| geneid | 27151 |
|---|---|
| ensemblid | ENSG00000160111.15 |
| hgncid | 23228 |
| symbol | CPAMD8 |
| name | C3 and PZP like alpha-2-macroglobulin domain containing 8 |
| refseq_nuc | NM_015692.5 |
| refseq_prot | NP_056507.3 |
| ensembl_nuc | ENST00000443236.7 |
| ensembl_prot | ENSP00000402505.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 16892951 |
| end | 17026810 |
| strand | - |
| ver | v1.2 |
| region | chr19:16892951-17026810 |
| region5000 | chr19:16887951-17031810 |
| regionname0 | CPAMD8_chr19_16892951_17026810 |
| regionname5000 | CPAMD8_chr19_16887951_17031810 |
| 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 | 0/0 | 1885 | 20 | 2 | 5 | 8 | 2 | 3 | 7 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002 | 0/0 | 1885 | 14 | 11 | 1 | 1 | 1 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0003 | 0/0 | 1885 | 12 | 0 | 2 | 7 | 0 | 3 | 5 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0004 | 0/0 | 1885 | 10 | 1 | 0 | 8 | 0 | 1 | 4 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0005 | 0/0 | 1885 | 9 | 0 | 3 | 4 | 0 | 2 | 3 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0006 | 0/1 | 1885 | 9 | 0 | 6 | 0 | 1 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007 | 0/0 | 1885 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0008 | 0/0 | 1885 | 6 | 0 | 3 | 2 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0009 | 0/0 | 1885 | 6 | 0 | 2 | 3 | 0 | 1 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0010 | 0/0 | 1885 | 6 | 1 | 4 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0011 | 0/0 | 1885 | 6 | 0 | 2 | 3 | 0 | 1 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0012 | 0/0 | 1885 | 5 | 0 | 2 | 1 | 0 | 2 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0013 | 0/0 | 1885 | 4 | 0 | 1 | 2 | 1 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0014 | 0/0 | 1885 | 4 | 0 | 0 | 3 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0015 | 0/0 | 1885 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0016 | 0/0 | 1885 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0017 | 0/0 | 1885 | 3 | 1 | 0 | 2 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0018 | 1/0 | 1885 | 3 | 0 | 1 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0019 | 0/0 | 1885 | 3 | 0 | 1 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0020 | 0/0 | 1885 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0021 | 0/0 | 1885 | 3 | 1 | 0 | 2 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0022 | 0/0 | 1885 | 3 | 0 | 0 | 1 | 0 | 2 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0023 | 0/0 | 1885 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0024 | 0/0 | 1885 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0025 | 0/0 | 1885 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0026 | 0/0 | 1885 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0027 | 0/0 | 1885 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0028 | 0/0 | 1885 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0029 | 0/0 | 1885 | 3 | 1 | 0 | 2 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0030 | 0/0 | 1885 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0031 | 0/0 | 1885 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0032 | 0/0 | 1885 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0033 | 0/0 | 1885 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0034 | 0/0 | 1885 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0035 | 0/0 | 1885 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0036 | 0/0 | 1885 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0037 | 0/0 | 1885 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0038 | 0/0 | 1885 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0039 | 0/0 | 1885 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0040 | 0/0 | 1885 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0041 | 0/0 | 1885 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0042 | 0/0 | 1885 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0043 | 0/0 | 1885 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0044 | 0/0 | 1885 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0045 | 0/0 | 1885 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0046 | 0/0 | 1885 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0047 | 0/0 | 1885 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0048 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0049 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0050 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0051 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0052 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0053 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0054 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0055 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0056 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0057 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0058 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0059 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0060 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0061 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0062 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0063 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0064 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0065 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0066 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0067 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0068 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0069 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0070 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0071 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0072 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0073 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0074 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0075 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0076 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0077 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0078 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0079 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0080 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0081 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0082 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0083 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0084 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0085 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0086 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0087 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0088 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0089 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0090 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0091 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0092 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0093 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0094 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0095 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0096 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0097 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0098 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0099 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0100 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0101 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0102 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0103 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0104 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0105 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0106 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0107 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0108 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0109 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0110 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0111 | 0/0 | 1885 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0112 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0113 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0114 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0115 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0116 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0117 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0118 | 0/0 | 1885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0119 | 0/0 | 1885 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0120 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0121 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0122 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0123 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0124 | 0/0 | 1885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| 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 | 5658 | 10 | 0 | 3 | 4 | 1 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0002 | 0/0 | 5658 | 9 | 0 | 1 | 5 | 0 | 3 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0003 | 0/0 | 5658 | 7 | 0 | 3 | 3 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0004 | 0/0 | 5658 | 6 | 1 | 4 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0005 | 0/0 | 5658 | 5 | 0 | 0 | 4 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0006 | 0/0 | 5658 | 5 | 0 | 4 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0007 | 0/0 | 5658 | 4 | 0 | 0 | 4 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0008 | 0/0 | 5658 | 4 | 0 | 2 | 0 | 2 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0009 | 0/0 | 5658 | 4 | 0 | 2 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0010 | 0/0 | 5658 | 4 | 0 | 2 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0011 | 0/0 | 5658 | 3 | 3 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0012 | 0/0 | 5658 | 3 | 0 | 1 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0013 | 0/0 | 5658 | 3 | 2 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0014 | 0/0 | 5658 | 3 | 0 | 0 | 3 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0015 | 0/1 | 5658 | 3 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0016 | 0/0 | 5658 | 3 | 1 | 2 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0017 | 0/0 | 5658 | 3 | 3 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0018 | 0/0 | 5658 | 3 | 3 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0019 | 0/0 | 5658 | 2 | 2 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0020 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0021 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0022 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0023 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0024 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0025 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0026 | 0/0 | 5658 | 2 | 0 | 2 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0027 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0028 | 0/0 | 5658 | 2 | 0 | 1 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0029 | 0/0 | 5658 | 2 | 0 | 0 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0030 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0031 | 0/0 | 5658 | 2 | 0 | 2 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0032 | 0/0 | 5658 | 2 | 0 | 0 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0033 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0034 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0035 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0036 | 0/0 | 5658 | 2 | 0 | 1 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0037 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0038 | 1/0 | 5658 | 2 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0039 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0040 | 0/0 | 5658 | 2 | 0 | 1 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0041 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0042 | 0/0 | 5658 | 2 | 0 | 0 | 1 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0043 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0044 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0045 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0046 | 0/0 | 5658 | 2 | 2 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0047 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0048 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0049 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0050 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0051 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0052 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0053 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0054 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0055 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0056 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0057 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0058 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0059 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0060 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0061 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0062 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0063 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0064 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0065 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0066 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0067 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0068 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0069 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0070 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0071 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0072 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0073 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0074 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0075 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0076 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0077 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0078 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0079 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0080 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0081 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0082 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0083 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0084 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0085 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0086 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0087 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0088 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0089 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0090 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0091 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0092 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0093 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0094 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0095 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0096 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0097 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0098 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0099 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0100 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0101 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0102 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0103 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0104 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0105 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0106 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0107 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0108 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0109 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0110 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0111 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0112 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0113 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0114 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0115 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0116 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0117 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0118 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0119 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0120 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0121 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0122 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0123 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0124 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0125 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0126 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0127 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0128 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0129 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0130 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0131 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0132 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0133 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0134 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0135 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0136 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0137 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0138 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0139 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0140 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0141 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0142 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0143 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0144 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0145 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0146 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0147 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0148 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0149 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0150 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0151 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0152 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0153 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0154 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0155 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0156 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0157 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0158 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0159 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0160 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0161 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0162 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0163 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0164 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0165 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0166 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0167 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0168 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0169 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0170 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0171 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0172 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0173 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0174 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0175 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0176 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0177 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0178 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0179 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0180 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0181 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0182 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0183 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0184 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0185 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| c0186 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 326 | 160 | 68 | 38 | 29 | 3 | 22 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| t0002 | 1/1 | 326 | 116 | 10 | 23 | 58 | 7 | 16 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| t0003 | 0/0 | 326 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| t0004 | 0/0 | 326 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| 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 | 5658 | 10 | 0 | 3 | 4 | 1 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0001c0007 | 0/0 | 5658 | 4 | 0 | 0 | 4 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0001c0013 | 0/0 | 5658 | 3 | 2 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0001c0033 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0001c0102 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0017 | 0/0 | 5658 | 3 | 3 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0018 | 0/0 | 5658 | 3 | 3 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0019 | 0/0 | 5658 | 2 | 2 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0056 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0058 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0059 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0062 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0120 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0176 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0003c0002 | 0/0 | 5658 | 9 | 0 | 1 | 5 | 0 | 3 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0003c0045 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0003c0151 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0004c0005 | 0/0 | 5658 | 5 | 0 | 0 | 4 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0004c0014 | 0/0 | 5658 | 3 | 0 | 0 | 3 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0004c0100 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0004c0180 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0005c0003 | 0/0 | 5658 | 7 | 0 | 3 | 3 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0005c0121 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0005c0131 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0006c0006 | 0/0 | 5658 | 5 | 0 | 4 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0006c0015 | 0/1 | 5658 | 3 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0006c0132 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007c0016 | 0/0 | 5658 | 3 | 1 | 2 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007c0052 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007c0053 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007c0119 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007c0170 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0008c0009 | 0/0 | 5658 | 4 | 0 | 2 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0008c0150 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0008c0160 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0009c0010 | 0/0 | 5658 | 4 | 0 | 2 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0009c0042 | 0/0 | 5658 | 2 | 0 | 0 | 1 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0010c0004 | 0/0 | 5658 | 6 | 1 | 4 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0011c0012 | 0/0 | 5658 | 3 | 0 | 1 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0011c0084 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0011c0090 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0011c0091 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0012c0028 | 0/0 | 5658 | 2 | 0 | 1 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0012c0029 | 0/0 | 5658 | 2 | 0 | 0 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0012c0083 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0013c0024 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0013c0049 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0013c0078 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0014c0027 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0014c0077 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0014c0105 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0015c0008 | 0/0 | 5658 | 4 | 0 | 2 | 0 | 2 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0016c0050 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0016c0116 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0016c0117 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0016c0185 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0017c0044 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0017c0147 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0018c0038 | 1/0 | 5658 | 2 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0018c0155 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0019c0039 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0019c0146 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0020c0011 | 0/0 | 5658 | 3 | 3 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0021c0037 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0021c0143 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0022c0032 | 0/0 | 5658 | 2 | 0 | 0 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0022c0106 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0023c0031 | 0/0 | 5658 | 2 | 0 | 2 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0023c0075 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0024c0030 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0024c0092 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0025c0020 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0025c0169 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0026c0034 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0026c0127 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0027c0035 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0027c0066 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0028c0114 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0028c0181 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0028c0182 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0029c0067 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0029c0125 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0029c0137 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0030c0166 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0030c0167 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0031c0041 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0032c0043 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0033c0040 | 0/0 | 5658 | 2 | 0 | 1 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0034c0070 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0034c0071 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0035c0026 | 0/0 | 5658 | 2 | 0 | 2 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0036c0025 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0037c0093 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0037c0104 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0038c0099 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0038c0109 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0039c0076 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0039c0107 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0040c0074 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0040c0141 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0041c0023 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0042c0174 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0042c0175 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0043c0022 | 0/0 | 5658 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0044c0021 | 0/0 | 5658 | 2 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0045c0051 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0045c0118 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0046c0036 | 0/0 | 5658 | 2 | 0 | 1 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0047c0046 | 0/0 | 5658 | 2 | 2 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0048c0168 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0049c0154 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0050c0148 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0051c0153 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0052c0152 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0053c0149 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0054c0159 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0055c0145 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0056c0072 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0057c0073 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0058c0158 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0059c0156 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0060c0157 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0061c0142 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0062c0069 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0063c0144 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0064c0161 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0065c0101 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0066c0103 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0067c0094 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0068c0095 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0069c0098 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0070c0096 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0071c0097 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0072c0081 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0073c0082 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0074c0080 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0075c0108 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0076c0088 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0077c0087 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0078c0086 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0079c0085 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0080c0089 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0081c0079 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0082c0165 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0083c0112 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0084c0111 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0085c0063 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0086c0179 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0087c0178 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0088c0047 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0089c0065 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0090c0064 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0091c0055 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0092c0173 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0093c0177 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0094c0060 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0095c0057 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0096c0061 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0097c0171 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0098c0172 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0099c0054 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0100c0068 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0101c0126 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0102c0130 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0103c0129 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0104c0133 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0105c0128 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0106c0134 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0107c0122 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0108c0183 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0109c0184 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0110c0115 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0111c0124 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0112c0135 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0113c0136 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0114c0113 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0115c0123 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0116c0138 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0117c0110 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0118c0139 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0119c0140 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0120c0164 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0121c0163 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0122c0162 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0123c0048 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0124c0186 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 5983 | 10 | 0 | 3 | 4 | 1 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0001c0007t0002 | 0/0 | 5983 | 4 | 0 | 0 | 4 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0001c0013t0001 | 0/0 | 5983 | 3 | 2 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0001c0033t0002 | 0/0 | 5983 | 2 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0001c0102t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0017t0001 | 0/0 | 5983 | 3 | 3 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0018t0001 | 0/0 | 5983 | 3 | 3 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0019t0001 | 0/0 | 5983 | 2 | 2 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0056t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0058t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0059t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0062t0002 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0120t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0002c0176t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0003c0002t0002 | 0/0 | 5983 | 9 | 0 | 1 | 5 | 0 | 3 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0003c0045t0002 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0003c0151t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0004c0005t0002 | 0/0 | 5983 | 5 | 0 | 0 | 4 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0004c0014t0002 | 0/0 | 5983 | 3 | 0 | 0 | 3 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0004c0100t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0004c0180t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0005c0003t0002 | 0/0 | 5983 | 7 | 0 | 3 | 3 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0005c0121t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0005c0131t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0006c0006t0001 | 0/0 | 5983 | 5 | 0 | 4 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0006c0015t0002 | 0/1 | 5983 | 3 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0006c0132t0002 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007c0016t0001 | 0/0 | 5983 | 3 | 1 | 2 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007c0052t0002 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007c0053t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007c0119t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0007c0170t0002 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0008c0009t0001 | 0/0 | 5983 | 4 | 0 | 2 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0008c0150t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0008c0160t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0009c0010t0002 | 0/0 | 5983 | 4 | 0 | 2 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0009c0042t0001 | 0/0 | 5983 | 2 | 0 | 0 | 1 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0010c0004t0001 | 0/0 | 5983 | 6 | 1 | 4 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0011c0012t0002 | 0/0 | 5983 | 3 | 0 | 1 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0011c0084t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0011c0090t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0011c0091t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0012c0028t0002 | 0/0 | 5983 | 2 | 0 | 1 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0012c0029t0001 | 0/0 | 5983 | 2 | 0 | 0 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0012c0083t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0013c0024t0002 | 0/0 | 5983 | 2 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0013c0049t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0013c0078t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0014c0027t0001 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0014c0077t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0014c0105t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0015c0008t0001 | 0/0 | 5983 | 3 | 0 | 1 | 0 | 2 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0015c0008t0004 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0016c0050t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0016c0116t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0016c0117t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0016c0185t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0017c0044t0001 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0017c0147t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0018c0038t0002 | 1/0 | 5983 | 2 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0018c0155t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0019c0039t0001 | 0/0 | 5983 | 2 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0019c0146t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0020c0011t0001 | 0/0 | 5983 | 3 | 3 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0021c0037t0002 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0021c0143t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0022c0032t0001 | 0/0 | 5983 | 2 | 0 | 0 | 0 | 0 | 2 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0022c0106t0003 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0023c0031t0001 | 0/0 | 5983 | 2 | 0 | 2 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0023c0075t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0024c0030t0001 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0024c0092t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0025c0020t0001 | 0/0 | 5983 | 2 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0025c0169t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0026c0034t0002 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0026c0127t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0027c0035t0001 | 0/0 | 5983 | 2 | 0 | 1 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0027c0066t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0028c0114t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0028c0181t0002 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0028c0182t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0029c0067t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0029c0125t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0029c0137t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0030c0166t0002 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0030c0167t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0031c0041t0001 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0032c0043t0001 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0033c0040t0001 | 0/0 | 5983 | 2 | 0 | 1 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0034c0070t0002 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0034c0071t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0035c0026t0001 | 0/0 | 5983 | 2 | 0 | 2 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0036c0025t0002 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0037c0093t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0037c0104t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0038c0099t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0038c0109t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0039c0076t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0039c0107t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0040c0074t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0040c0141t0002 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0041c0023t0002 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0042c0174t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0042c0175t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0043c0022t0001 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0044c0021t0002 | 0/0 | 5983 | 2 | 0 | 1 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0045c0051t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0045c0118t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0046c0036t0001 | 0/0 | 5983 | 2 | 0 | 1 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0047c0046t0002 | 0/0 | 5983 | 2 | 2 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0048c0168t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0049c0154t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0050c0148t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0051c0153t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0052c0152t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0053c0149t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0054c0159t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0055c0145t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0056c0072t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0057c0073t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0058c0158t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0059c0156t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0060c0157t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0061c0142t0002 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0062c0069t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0063c0144t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0064c0161t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0065c0101t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0066c0103t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0067c0094t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0068c0095t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0069c0098t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0070c0096t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0071c0097t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0072c0081t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0073c0082t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0074c0080t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0075c0108t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0076c0088t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0077c0087t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0078c0086t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0079c0085t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0080c0089t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0081c0079t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0082c0165t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0083c0112t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0084c0111t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0085c0063t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0086c0179t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0087c0178t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0088c0047t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0089c0065t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0090c0064t0002 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0091c0055t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0092c0173t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0093c0177t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0094c0060t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0095c0057t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0096c0061t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0097c0171t0002 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0098c0172t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0099c0054t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0100c0068t0002 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0101c0126t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0102c0130t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0103c0129t0001 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0104c0133t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0105c0128t0002 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0106c0134t0001 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0107c0122t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0108c0183t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0109c0184t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0110c0115t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0111c0124t0002 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0112c0135t0002 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0113c0136t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0114c0113t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0115c0123t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0116c0138t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0117c0110t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0118c0139t0001 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0119c0140t0002 | 0/0 | 5983 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0120c0164t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0121c0163t0002 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0122c0162t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0123c0048t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| a0124c0186t0001 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | copy fasta | chr19 | 16887951 | 17031810 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0007t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0007t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0007t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0007t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0013t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0013t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0013t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0033t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0033t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0001c0102t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0017t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0017t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0017t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0018t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0018t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0018t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0019t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0019t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0056t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0058t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0059t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0062t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0120t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0002c0176t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0045t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0045t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0003c0151t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0004c0005t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0004c0005t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0004c0005t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0004c0005t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0004c0005t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0004c0014t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0004c0014t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0004c0014t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0004c0100t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0004c0180t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0005c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0005c0003t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0005c0003t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0005c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0005c0003t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0005c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0005c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0005c0121t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0005c0131t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0006c0006t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0006c0006t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0006c0006t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0006c0006t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0006c0006t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0006c0015t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0006c0015t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0006c0015t0002g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0006c0132t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0007c0016t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0007c0016t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0007c0016t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0007c0052t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0007c0053t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0007c0119t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0007c0170t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0008c0009t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0008c0009t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0008c0009t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0008c0009t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0008c0150t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0008c0160t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0009c0010t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0009c0010t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0009c0010t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0009c0010t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0009c0042t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0009c0042t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0010c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0010c0004t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0010c0004t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0010c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0010c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0010c0004t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0011c0012t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0011c0012t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0011c0012t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0011c0084t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0011c0090t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0011c0091t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0012c0028t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0012c0028t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0012c0029t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0012c0029t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0012c0083t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0013c0024t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0013c0024t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0013c0049t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0013c0078t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0014c0027t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0014c0027t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0014c0077t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0014c0105t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0015c0008t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0015c0008t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0015c0008t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0015c0008t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0016c0050t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0016c0116t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0016c0117t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0016c0185t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0017c0044t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0017c0044t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0017c0147t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0018c0038t0002g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0018c0038t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0018c0155t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0019c0039t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0019c0039t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0019c0146t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0020c0011t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0020c0011t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0020c0011t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0021c0037t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0021c0037t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0021c0143t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0022c0032t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0022c0032t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0022c0106t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0023c0031t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0023c0031t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0023c0075t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0024c0030t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0024c0030t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0024c0092t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0025c0020t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0025c0020t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0025c0169t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0026c0034t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0026c0034t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0026c0127t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0027c0035t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0027c0035t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0027c0066t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0028c0114t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0028c0181t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0028c0182t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0029c0067t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0029c0125t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0029c0137t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0030c0166t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0030c0167t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0031c0041t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0031c0041t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0032c0043t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0032c0043t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0033c0040t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0033c0040t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0034c0070t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0034c0071t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0035c0026t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0035c0026t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0036c0025t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0036c0025t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0037c0093t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0037c0104t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0038c0099t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0038c0109t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0039c0076t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0039c0107t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0040c0074t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0040c0141t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0041c0023t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0041c0023t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0042c0174t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0042c0175t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0043c0022t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0043c0022t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0044c0021t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0044c0021t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0045c0051t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0045c0118t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0046c0036t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0046c0036t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0047c0046t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0047c0046t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0048c0168t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0049c0154t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0050c0148t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0051c0153t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0052c0152t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0053c0149t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0054c0159t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0055c0145t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0056c0072t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0057c0073t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0058c0158t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0059c0156t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0060c0157t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0061c0142t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0062c0069t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0063c0144t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0064c0161t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0065c0101t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0066c0103t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0067c0094t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0068c0095t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0069c0098t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0070c0096t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0071c0097t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0072c0081t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0073c0082t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0074c0080t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0075c0108t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0076c0088t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0077c0087t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0078c0086t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0079c0085t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0080c0089t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0081c0079t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0082c0165t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0083c0112t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0084c0111t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0085c0063t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0086c0179t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0087c0178t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0088c0047t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0089c0065t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0090c0064t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0091c0055t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0092c0173t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0093c0177t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0094c0060t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0095c0057t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0096c0061t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0097c0171t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0098c0172t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0099c0054t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0100c0068t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0101c0126t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0102c0130t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0103c0129t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0104c0133t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0105c0128t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0106c0134t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0107c0122t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0108c0183t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0109c0184t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0110c0115t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0111c0124t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0112c0135t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0113c0136t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0114c0113t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0115c0123t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0116c0138t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0117c0110t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0118c0139t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0119c0140t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0120c0164t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0121c0163t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0122c0162t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0123c0048t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| a0124c0186t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0248 | EUR | GBR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00099 | hp2 | a0001 | c0033 | t0002 | g0027 | EUR | GBR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00140 | hp1 | a0006 | c0015 | t0002 | g0133 | EUR | GBR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00140 | hp2 | a0095 | c0057 | t0002 | g0134 | EUR | GBR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00423 | hp1 | a0003 | c0002 | t0002 | g0252 | EAS | CHS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00423 | hp2 | a0013 | c0078 | t0002 | g0171 | EAS | CHS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00438 | hp1 | a0077 | c0087 | t0001 | g0225 | EAS | CHS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00438 | hp2 | a0021 | c0037 | t0002 | g0256 | EAS | CHS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00597 | hp1 | a0058 | c0158 | t0001 | g0230 | EAS | CHS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00597 | hp2 | a0014 | c0027 | t0001 | g0175 | EAS | CHS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00609 | hp1 | a0019 | c0146 | t0001 | g0198 | EAS | CHS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00609 | hp2 | a0079 | c0085 | t0001 | g0047 | EAS | CHS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00639 | hp1 | a0037 | c0104 | t0001 | g0150 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00639 | hp2 | a0112 | c0135 | t0002 | g0268 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00642 | hp1 | a0090 | c0064 | t0002 | g0144 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00642 | hp2 | a0033 | c0040 | t0001 | g0265 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00735 | hp1 | a0015 | c0008 | t0004 | g0278 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00735 | hp2 | a0076 | c0088 | t0001 | g0084 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00741 | hp1 | a0001 | c0033 | t0002 | g0002 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG00741 | hp2 | a0118 | c0139 | t0001 | g0108 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01070 | hp1 | a0115 | c0123 | t0001 | g0226 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01070 | hp2 | a0023 | c0031 | t0001 | g0025 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01071 | hp1 | a0008 | c0009 | t0001 | g0247 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01071 | hp2 | a0023 | c0031 | t0001 | g0026 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01081 | hp1 | a0006 | c0006 | t0001 | g0086 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01081 | hp2 | a0027 | c0035 | t0001 | g0045 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01099 | hp1 | a0040 | c0141 | t0002 | g0245 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01099 | hp2 | a0012 | c0083 | t0001 | g0132 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01109 | hp1 | a0034 | c0070 | t0002 | g0091 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01109 | hp2 | a0010 | c0004 | t0001 | g0254 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01167 | hp1 | a0007 | c0016 | t0001 | g0123 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01167 | hp2 | a0116 | c0138 | t0001 | g0028 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01168 | hp1 | a0035 | c0026 | t0001 | g0234 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01168 | hp2 | a0008 | c0150 | t0001 | g0273 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01169 | hp1 | a0035 | c0026 | t0001 | g0233 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01169 | hp2 | a0007 | c0016 | t0001 | g0124 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01175 | hp1 | a0044 | c0021 | t0002 | g0269 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01175 | hp2 | a0105 | c0128 | t0002 | g0127 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01192 | hp1 | a0015 | c0008 | t0001 | g0035 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01192 | hp2 | a0001 | c0013 | t0001 | g0261 | AMR | PUR | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01256 | hp1 | a0037 | c0093 | t0001 | g0274 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01256 | hp2 | a0009 | c0010 | t0002 | g0208 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01257 | hp1 | a0078 | c0086 | t0001 | g0242 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01257 | hp2 | a0008 | c0009 | t0001 | g0217 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01258 | hp1 | a0009 | c0010 | t0002 | g0209 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01258 | hp2 | a0010 | c0004 | t0001 | g0243 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01261 | hp1 | a0046 | c0036 | t0001 | g0204 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01261 | hp2 | a0006 | c0006 | t0001 | g0131 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01346 | hp1 | a0006 | c0132 | t0002 | g0087 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01346 | hp2 | a0003 | c0151 | t0001 | g0143 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01361 | hp1 | a0107 | c0122 | t0001 | g0023 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01361 | hp2 | a0005 | c0003 | t0002 | g0166 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01433 | hp1 | a0018 | c0038 | t0002 | g0193 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01496 | hp1 | a0005 | c0003 | t0002 | g0125 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01496 | hp2 | a0013 | c0024 | t0002 | g0178 | AMR | CLM | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01515 | hp1 | a0015 | c0008 | t0001 | g0005 | EUR | IBS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01515 | hp2 | a0013 | c0024 | t0002 | g0275 | EUR | IBS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01516 | hp1 | a0015 | c0008 | t0001 | g0174 | EUR | IBS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01516 | hp2 | a0082 | c0165 | t0002 | g0214 | EUR | IBS | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01884 | hp1 | a0124 | c0186 | t0001 | g0049 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01884 | hp2 | a0061 | c0142 | t0002 | g0015 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01891 | hp1 | a0001 | c0013 | t0001 | g0090 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01891 | hp2 | a0100 | c0068 | t0002 | g0159 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01928 | hp1 | a0010 | c0004 | t0001 | g0089 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01928 | hp2 | a0025 | c0169 | t0001 | g0120 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01934 | hp1 | a0025 | c0020 | t0001 | g0153 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01934 | hp2 | a0002 | c0062 | t0002 | g0176 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01975 | hp1 | a0039 | c0076 | t0001 | g0126 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01975 | hp2 | a0006 | c0015 | t0002 | g0110 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01978 | hp1 | a0019 | c0039 | t0001 | g0227 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01978 | hp2 | a0003 | c0002 | t0002 | g0196 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01981 | hp1 | a0006 | c0006 | t0001 | g0220 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01993 | hp1 | a0011 | c0012 | t0002 | g0207 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG01993 | hp2 | a0010 | c0004 | t0001 | g0088 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02015 | hp1 | a0014 | c0027 | t0001 | g0180 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02015 | hp2 | a0008 | c0009 | t0001 | g0197 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02027 | hp1 | a0022 | c0106 | t0003 | g0155 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02027 | hp2 | a0036 | c0025 | t0002 | g0264 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02040 | hp1 | a0005 | c0003 | t0002 | g0167 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02040 | hp2 | a0004 | c0005 | t0002 | g0146 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02055 | hp1 | a0020 | c0011 | t0001 | g0021 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02055 | hp2 | a0110 | c0115 | t0001 | g0098 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02056 | hp1 | a0017 | c0044 | t0001 | g0076 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02056 | hp2 | a0003 | c0002 | t0002 | g0092 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02074 | hp1 | a0009 | c0010 | t0002 | g0078 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02074 | hp2 | a0011 | c0091 | t0001 | g0179 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02083 | hp1 | a0004 | c0014 | t0002 | g0223 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02083 | hp2 | a0014 | c0077 | t0001 | g0249 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02129 | hp1 | a0004 | c0014 | t0002 | g0038 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02129 | hp2 | a0031 | c0041 | t0001 | g0253 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02132 | hp1 | a0001 | c0007 | t0002 | g0246 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02132 | hp2 | a0017 | c0044 | t0001 | g0077 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02135 | hp1 | a0104 | c0133 | t0002 | g0241 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02135 | hp2 | a0008 | c0009 | t0001 | g0231 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02145 | hp1 | a0020 | c0011 | t0001 | g0017 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02145 | hp2 | a0048 | c0168 | t0001 | g0272 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02148 | hp1 | a0051 | c0153 | t0001 | g0237 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02148 | hp2 | a0005 | c0003 | t0002 | g0236 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02155 | hp1 | a0080 | c0089 | t0002 | g0250 | EAS | CDX | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02155 | hp2 | a0096 | c0061 | t0001 | g0168 | EAS | CDX | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02257 | hp1 | a0042 | c0175 | t0001 | g0075 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02257 | hp2 | a0001 | c0013 | t0001 | g0138 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02293 | hp1 | a0011 | c0084 | t0001 | g0181 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02293 | hp2 | a0012 | c0028 | t0002 | g0177 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02300 | hp2 | a0006 | c0006 | t0001 | g0205 | AMR | PEL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02451 | hp1 | a0097 | c0171 | t0002 | g0163 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02451 | hp2 | a0086 | c0179 | t0001 | g0102 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02523 | hp1 | a0029 | c0137 | t0002 | g0270 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02523 | hp2 | a0004 | c0014 | t0002 | g0222 | EAS | KHV | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02572 | hp1 | a0016 | c0185 | t0001 | g0058 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02572 | hp2 | a0074 | c0080 | t0001 | g0082 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02602 | hp1 | a0060 | c0157 | t0002 | g0142 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02602 | hp2 | a0089 | c0065 | t0002 | g0130 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02615 | hp1 | a0002 | c0017 | t0001 | g0113 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02615 | hp2 | a0057 | c0073 | t0001 | g0066 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02622 | hp1 | a0002 | c0019 | t0001 | g0139 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02622 | hp2 | a0002 | c0018 | t0001 | g0115 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02647 | hp1 | a0028 | c0182 | t0001 | g0062 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02647 | hp2 | a0088 | c0047 | t0001 | g0161 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02683 | hp1 | a0064 | c0161 | t0002 | g0187 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02683 | hp2 | a0083 | c0112 | t0001 | g0096 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02698 | hp1 | a0008 | c0160 | t0001 | g0040 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02698 | hp2 | a0049 | c0154 | t0001 | g0195 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02717 | hp1 | a0055 | c0145 | t0001 | g0093 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02717 | hp2 | a0002 | c0018 | t0001 | g0116 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02735 | hp1 | a0025 | c0020 | t0001 | g0104 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02735 | hp2 | a0009 | c0042 | t0001 | g0194 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02809 | hp1 | a0108 | c0183 | t0001 | g0056 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02809 | hp2 | a0016 | c0117 | t0001 | g0114 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02818 | hp1 | a0002 | c0018 | t0001 | g0099 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02818 | hp2 | a0114 | c0113 | t0001 | g0101 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02886 | hp1 | a0002 | c0176 | t0001 | g0014 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02886 | hp2 | a0007 | c0119 | t0001 | g0122 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02895 | hp1 | a0002 | c0017 | t0001 | g0112 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02895 | hp2 | a0047 | c0046 | t0002 | g0135 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02897 | hp1 | a0047 | c0046 | t0002 | g0136 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02897 | hp2 | a0081 | c0079 | t0001 | g0080 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02922 | hp1 | a0007 | c0170 | t0002 | g0117 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02922 | hp2 | a0045 | c0118 | t0001 | g0024 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02965 | hp1 | a0109 | c0184 | t0001 | g0057 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02965 | hp2 | a0098 | c0172 | t0001 | g0006 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02976 | hp1 | a0030 | c0167 | t0001 | g0271 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02976 | hp2 | a0073 | c0082 | t0001 | g0069 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03098 | hp1 | a0056 | c0072 | t0001 | g0094 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03098 | hp2 | a0010 | c0004 | t0001 | g0068 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03130 | hp1 | a0042 | c0174 | t0001 | g0160 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03130 | hp2 | a0069 | c0098 | t0001 | g0065 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03195 | hp1 | a0016 | c0116 | t0001 | g0010 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03195 | hp2 | a0101 | c0126 | t0001 | g0061 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03209 | hp1 | a0007 | c0052 | t0002 | g0119 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03209 | hp2 | a0063 | c0144 | t0001 | g0118 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03239 | hp1 | a0019 | c0039 | t0001 | g0238 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03239 | hp2 | a0027 | c0066 | t0001 | g0016 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03453 | hp1 | a0120 | c0164 | t0001 | g0013 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03453 | hp2 | a0002 | c0019 | t0001 | g0008 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03486 | hp1 | a0121 | c0163 | t0002 | g0107 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03486 | hp2 | a0021 | c0143 | t0001 | g0012 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03490 | hp1 | a0012 | c0029 | t0001 | g0151 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03490 | hp2 | a0113 | c0136 | t0002 | g0169 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03491 | hp1 | a0075 | c0108 | t0001 | g0141 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03491 | hp2 | a0022 | c0032 | t0001 | g0229 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03492 | hp1 | a0012 | c0029 | t0001 | g0152 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03492 | hp2 | a0022 | c0032 | t0001 | g0228 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03516 | hp1 | a0028 | c0181 | t0002 | g0060 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03516 | hp2 | a0062 | c0069 | t0001 | g0071 | AFR | ESN | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03540 | hp1 | a0065 | c0101 | t0001 | g0001 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03540 | hp2 | a0045 | c0051 | t0001 | g0083 | AFR | GWD | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03579 | hp1 | a0072 | c0081 | t0001 | g0067 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03579 | hp2 | a0117 | c0110 | t0001 | g0055 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03669 | hp1 | a0004 | c0005 | t0002 | g0211 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03669 | hp2 | a0014 | c0105 | t0001 | g0140 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03688 | hp1 | a0003 | c0002 | t0002 | g0105 | SAS | STU | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03688 | hp2 | a0094 | c0060 | t0001 | g0262 | SAS | STU | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03704 | hp1 | a0119 | c0140 | t0002 | g0111 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03704 | hp2 | a0006 | c0006 | t0001 | g0183 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03710 | hp1 | a0005 | c0121 | t0002 | g0267 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03927 | hp1 | a0066 | c0103 | t0002 | g0022 | SAS | BEB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03927 | hp2 | a0084 | c0111 | t0001 | g0097 | SAS | BEB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | STU | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG04115 | hp2 | a0003 | c0002 | t0002 | g0154 | SAS | STU | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG04184 | hp1 | a0005 | c0003 | t0002 | g0244 | SAS | BEB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG04184 | hp2 | a0039 | c0107 | t0001 | g0184 | SAS | BEB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG04199 | hp1 | a0010 | c0004 | t0001 | g0201 | SAS | STU | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG04199 | hp2 | a0001 | c0102 | t0002 | g0079 | SAS | STU | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG04204 | hp1 | a0011 | c0090 | t0001 | g0255 | SAS | STU | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG04204 | hp2 | a0003 | c0002 | t0002 | g0200 | SAS | STU | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG04228 | hp1 | a0103 | c0129 | t0001 | g0129 | SAS | STU | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG04228 | hp2 | a0044 | c0021 | t0002 | g0085 | SAS | STU | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18522 | hp1 | a0030 | c0166 | t0002 | g0059 | AFR | YRI | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18522 | hp2 | a0034 | c0071 | t0001 | g0070 | AFR | YRI | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18612 | hp1 | a0111 | c0124 | t0002 | g0050 | EAS | CHB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18612 | hp2 | a0024 | c0092 | t0001 | g0260 | EAS | CHB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18906 | hp1 | a0002 | c0056 | t0001 | g0081 | AFR | YRI | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18906 | hp2 | a0085 | c0063 | t0001 | g0018 | AFR | YRI | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18943 | hp1 | a0043 | c0022 | t0001 | g0232 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18943 | hp2 | a0041 | c0023 | t0002 | g0258 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18944 | hp1 | a0067 | c0094 | t0002 | g0145 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18944 | hp2 | a0059 | c0156 | t0002 | g0259 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18947 | hp1 | a0032 | c0043 | t0001 | g0037 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18949 | hp1 | a0038 | c0099 | t0002 | g0224 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18950 | hp1 | a0031 | c0041 | t0001 | g0216 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18950 | hp2 | a0012 | c0028 | t0002 | g0073 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18959 | hp1 | a0003 | c0002 | t0002 | g0186 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18959 | hp2 | a0106 | c0134 | t0001 | g0109 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18963 | hp1 | a0052 | c0152 | t0002 | g0029 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18963 | hp2 | a0002 | c0059 | t0001 | g0044 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18965 | hp1 | a0046 | c0036 | t0001 | g0031 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18965 | hp2 | a0009 | c0042 | t0001 | g0206 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18966 | hp1 | a0011 | c0012 | t0002 | g0202 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18966 | hp2 | a0070 | c0096 | t0002 | g0251 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18971 | hp1 | a0040 | c0074 | t0002 | g0212 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18979 | hp1 | a0001 | c0007 | t0002 | g0053 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18979 | hp2 | a0038 | c0109 | t0002 | g0165 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18985 | hp1 | a0004 | c0100 | t0002 | g0054 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18985 | hp2 | a0005 | c0003 | t0002 | g0051 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18992 | hp1 | a0102 | c0130 | t0002 | g0030 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA18992 | hp2 | a0036 | c0025 | t0002 | g0189 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19000 | hp1 | a0029 | c0125 | t0002 | g0034 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19000 | hp2 | a0071 | c0097 | t0001 | g0182 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19002 | hp1 | a0053 | c0149 | t0001 | g0106 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19002 | hp2 | a0004 | c0005 | t0002 | g0042 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19007 | hp1 | a0043 | c0022 | t0001 | g0203 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19007 | hp2 | a0003 | c0002 | t0002 | g0039 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19010 | hp1 | a0001 | c0007 | t0002 | g0036 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19010 | hp2 | a0013 | c0049 | t0002 | g0170 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19011 | hp1 | a0021 | c0037 | t0002 | g0190 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19011 | hp2 | a0024 | c0030 | t0001 | g0173 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19012 | hp1 | a0001 | c0007 | t0002 | g0221 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19012 | hp2 | a0003 | c0045 | t0002 | g0218 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19030 | hp1 | a0123 | c0048 | t0001 | g0011 | AFR | LWK | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19030 | hp2 | a0002 | c0120 | t0001 | g0074 | AFR | LWK | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19043 | hp1 | a0029 | c0067 | t0001 | g0004 | AFR | LWK | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19043 | hp2 | a0007 | c0053 | t0001 | g0156 | AFR | LWK | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19065 | hp1 | a0041 | c0023 | t0002 | g0157 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19065 | hp2 | a0026 | c0034 | t0002 | g0032 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19066 | hp1 | a0033 | c0040 | t0001 | g0043 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19066 | hp2 | a0003 | c0002 | t0002 | g0213 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19067 | hp1 | a0026 | c0034 | t0002 | g0033 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19067 | hp2 | a0004 | c0005 | t0002 | g0188 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19070 | hp1 | a0011 | c0012 | t0002 | g0210 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19070 | hp2 | a0032 | c0043 | t0001 | g0191 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19074 | hp1 | a0005 | c0003 | t0002 | g0239 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19074 | hp2 | a0009 | c0010 | t0002 | g0257 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19081 | hp1 | a0003 | c0045 | t0002 | g0052 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19085 | hp1 | a0024 | c0030 | t0001 | g0148 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19085 | hp2 | a0050 | c0148 | t0002 | g0235 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19088 | hp1 | a0068 | c0095 | t0002 | g0064 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19088 | hp2 | a0018 | c0155 | t0002 | g0215 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19090 | hp1 | a0005 | c0131 | t0002 | g0063 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19090 | hp2 | a0004 | c0005 | t0002 | g0046 | EAS | JPT | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19240 | hp1 | a0092 | c0173 | t0001 | g0164 | AFR | YRI | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA19240 | hp2 | a0028 | c0114 | t0001 | g0100 | AFR | YRI | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA20129 | hp1 | a0023 | c0075 | t0001 | g0137 | AFR | ASW | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA20129 | hp2 | a0017 | c0147 | t0001 | g0009 | AFR | ASW | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA20805 | hp1 | a0027 | c0035 | t0001 | g0172 | EUR | TSI | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA20805 | hp2 | a0002 | c0058 | t0002 | g0149 | EUR | TSI | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA20905 | hp1 | a0054 | c0159 | t0001 | g0128 | SAS | GIH | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA20905 | hp2 | a0026 | c0127 | t0001 | g0240 | SAS | GIH | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02109 | hp1 | a0002 | c0017 | t0001 | g0162 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02109 | hp2 | a0007 | c0016 | t0001 | g0007 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02486 | hp1 | a0020 | c0011 | t0001 | g0020 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02486 | hp2 | a0099 | c0054 | t0001 | g0003 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02559 | hp1 | a0087 | c0178 | t0001 | g0103 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG02559 | hp2 | a0016 | c0050 | t0001 | g0095 | AFR | ACB | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03471 | hp1 | a0122 | c0162 | t0001 | g0019 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| HG03471 | hp2 | a0093 | c0177 | t0001 | g0072 | AFR | MSL | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA21309 | hp1 | a0004 | c0180 | t0001 | g0041 | AFR | LWK | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| NA21309 | hp2 | a0091 | c0055 | t0001 | g0121 | AFR | LWK | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| homoSapiens_chm13v2 | hp1 | a0006 | c0015 | t0002 | g0263 | REF | REF | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| homoSapiens_grch38 | hp1 | a0018 | c0038 | t0002 | g0192 | REF | REF | CPAMD8_chr19_16887951_17031810 | CPAMD8 | chr19 | 16887951 | 17031810 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16893238
|
T | C | 28 | a0008a0010a0015others(25): Show | 54 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(51): Show |
missense_variant | MODERATE | c.5528A>G | p.Gln1843Arg | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 42/42 | 5696/5983 | 5528/5658 | 1843/1885 | chr19 | 16893238 | ||
| chr19:16893308
|
T | C | 1 | a0097 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.5458A>G | p.Ser1820Gly | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 42/42 | 5626/5983 | 5458/5658 | 1820/1885 | chr19 | 16893308 | ||
| chr19:16896552
|
C | T | 9 | a0031a0055a0058others(6): Show | 10 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(7): Show |
missense_variant | MODERATE | c.5179G>A | p.Asp1727Asn | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 40/42 | 5347/5983 | 5179/5658 | 1727/1885 | chr19 | 16896552 | ||
| chr19:16896567
|
G | T | 2 | a0095a0112 | 2 | HG00140.hp2 HG00639.hp2 |
missense_variant | MODERATE | c.5164C>A | p.Pro1722Thr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 40/42 | 5332/5983 | 5164/5658 | 1722/1885 | chr19 | 16896567 | ||
| chr19:16897748
|
C | T | 1 | a0105 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.5008G>A | p.Glu1670Lys | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/42 | 5176/5983 | 5008/5658 | 1670/1885 | chr19 | 16897748 | ||
| chr19:16902674
|
T | C | 3 | a0052a0070a0104 | 3 | HG02135.hp1 NA18963.hp1 NA18966.hp2 |
missense_variant | MODERATE | c.4660A>G | p.Lys1554Glu | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/42 | 4828/5983 | 4660/5658 | 1554/1885 | chr19 | 16902674 | ||
| chr19:16902736
|
C | T | 1 | a0066 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.4598G>A | p.Arg1533Gln | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/42 | 4766/5983 | 4598/5658 | 1533/1885 | chr19 | 16902736 | ||
| chr19:16902845
|
C | A | 1 | a0063 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.4489G>T | p.Val1497Leu | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/42 | 4657/5983 | 4489/5658 | 1497/1885 | chr19 | 16902845 | ||
| chr19:16907068
|
G | A | 24 | a0006a0009a0011others(21): Show | 55 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(52): Show |
missense_variant | MODERATE | c.3911C>T | p.Ala1304Val | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/42 | 4079/5983 | 3911/5658 | 1304/1885 | chr19 | 16907068 | ||
| chr19:16914482
|
G | A | 83 | a0001a0002a0003others(80): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
missense_variant | MODERATE | c.3803C>T | p.Thr1268Ile | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/42 | 3971/5983 | 3803/5658 | 1268/1885 | chr19 | 16914482 | ||
| chr19:16925214
|
T | C | 1 | a0103 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.3529A>G | p.Thr1177Ala | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/42 | 3697/5983 | 3529/5658 | 1177/1885 | chr19 | 16925214 | ||
| chr19:16925277
|
C | T | 20 | a0017a0023a0028others(17): Show | 27 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(24): Show |
missense_variant | MODERATE | c.3466G>A | p.Val1156Ile | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/42 | 3634/5983 | 3466/5658 | 1156/1885 | chr19 | 16925277 | ||
| chr19:16928213
|
A | C | 4 | a0030a0035a0062others(1): Show | 6 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(3): Show |
missense_variant | MODERATE | c.3166T>G | p.Ser1056Ala | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/42 | 3334/5983 | 3166/5658 | 1056/1885 | chr19 | 16928213 | ||
| chr19:16938433
|
G | A | 1 | a0093 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.2807C>T | p.Pro936Leu | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/42 | 2975/5983 | 2807/5658 | 936/1885 | chr19 | 16938433 | ||
| chr19:16945565
|
C | T | 5 | a0055a0065a0085others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
missense_variant | MODERATE | c.2777G>A | p.Arg926His | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/42 | 2945/5983 | 2777/5658 | 926/1885 | chr19 | 16945565 | ||
| chr19:16947150
|
C | A | 1 | a0076 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.2586G>T | p.Met862Ile | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/42 | 2754/5983 | 2586/5658 | 862/1885 | chr19 | 16947150 | ||
| chr19:16947211
|
G | A | 1 | a0049 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.2525C>T | p.Ser842Leu | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/42 | 2693/5983 | 2525/5658 | 842/1885 | chr19 | 16947211 | ||
| chr19:16951974
|
C | T | 5 | a0028a0074a0088others(2): Show | 7 | HG02572.hp2 HG02647.hp1 HG02647.hp2 others(4): Show |
missense_variant | MODERATE | c.2503G>A | p.Ala835Thr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/42 | 2671/5983 | 2503/5658 | 835/1885 | chr19 | 16951974 | ||
| chr19:16952010
|
T | C | 2 | a0099a0107 | 2 | HG01361.hp1 HG02486.hp2 |
missense_variant | MODERATE | c.2467A>G | p.Ile823Val | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/42 | 2635/5983 | 2467/5658 | 823/1885 | chr19 | 16952010 | ||
| chr19:16952049
|
T | C | 1 | a0080 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.2428A>G | p.Met810Val | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/42 | 2596/5983 | 2428/5658 | 810/1885 | chr19 | 16952049 | ||
| chr19:16970895
|
G | C | 2 | a0054a0075 | 2 | HG03491.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.2209C>G | p.Pro737Ala | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/42 | 2377/5983 | 2209/5658 | 737/1885 | chr19 | 16970895 | ||
| chr19:16970897
|
G | T | 22 | a0020a0028a0045others(19): Show | 27 | HG00741.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
missense_variant | MODERATE | c.2207C>A | p.Pro736His | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/42 | 2375/5983 | 2207/5658 | 736/1885 | chr19 | 16970897 | ||
| chr19:16971007
|
G | T | 5 | a0034a0081a0087others(2): Show | 6 | HG01109.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
missense_variant | MODERATE | c.2097C>A | p.Asp699Glu | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/42 | 2265/5983 | 2097/5658 | 699/1885 | chr19 | 16971007 | ||
| chr19:16975213
|
C | T | 2 | a0066a0067 | 2 | HG03927.hp1 NA18944.hp1 |
missense_variant | MODERATE | c.1954G>A | p.Val652Met | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/42 | 2122/5983 | 1954/5658 | 652/1885 | chr19 | 16975213 | ||
| chr19:16977386
|
C | G | 2 | a0030a0048 | 3 | HG02145.hp2 HG02976.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1740G>C | p.Glu580Asp | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/42 | 1908/5983 | 1740/5658 | 580/1885 | chr19 | 16977386 | ||
| chr19:16977489
|
T | C | 82 | a0001a0002a0004others(79): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
missense_variant | MODERATE | c.1637A>G | p.His546Arg | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/42 | 1805/5983 | 1637/5658 | 546/1885 | chr19 | 16977489 | ||
| chr19:16977509
|
G | T | 38 | a0001a0007a0010others(35): Show | 91 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(88): Show |
missense_variant | MODERATE | c.1617C>A | p.Asp539Glu | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/42 | 1785/5983 | 1617/5658 | 539/1885 | chr19 | 16977509 | ||
| chr19:16980571
|
G | A | 8 | a0065a0083a0084others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
missense_variant | MODERATE | c.1511C>T | p.Thr504Ile | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/42 | 1679/5983 | 1511/5658 | 504/1885 | chr19 | 16980571 | ||
| chr19:16993429
|
T | C | 1 | a0116 | 1 | HG01167.hp2 | missense_variant | MODERATE | c.1253A>G | p.His418Arg | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/42 | 1421/5983 | 1253/5658 | 418/1885 | chr19 | 16993429 | ||
| chr19:16997212
|
C | T | 3 | a0040a0041a0082 | 5 | HG01099.hp1 HG01516.hp2 NA18943.hp2 others(2): Show |
missense_variant | MODERATE | c.994G>A | p.Ala332Thr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1162/5983 | 994/5658 | 332/1885 | chr19 | 16997212 | ||
| chr19:16997242
|
C | T | 4 | a0083a0084a0118others(1): Show | 4 | HG00741.hp2 HG02683.hp2 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.964G>A | p.Val322Met | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1132/5983 | 964/5658 | 322/1885 | chr19 | 16997242 | ||
| chr19:16997243
|
C | T | 24 | a0002a0007a0025others(21): Show | 50 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(47): Show |
missense_variant | MODERATE | c.963G>A | p.Met321Ile | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1131/5983 | 963/5658 | 321/1885 | chr19 | 16997243 | ||
| chr19:16997284
|
C | T | 4 | a0083a0084a0118others(1): Show | 4 | HG00741.hp2 HG02683.hp2 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.922G>A | p.Val308Ile | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1090/5983 | 922/5658 | 308/1885 | chr19 | 16997284 | ||
| chr19:16997289
|
G | A | 1 | a0064 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.917C>T | p.Ala306Val | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1085/5983 | 917/5658 | 306/1885 | chr19 | 16997289 | ||
| chr19:16997317
|
C | T | 1 | a0117 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.889G>A | p.Asp297Asn | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1057/5983 | 889/5658 | 297/1885 | chr19 | 16997317 | ||
| chr19:16997325
|
C | T | 36 | a0001a0004a0010others(33): Show | 97 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(94): Show |
missense_variant | MODERATE | c.881G>A | p.Arg294Gln | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1049/5983 | 881/5658 | 294/1885 | chr19 | 16997325 | ||
| chr19:16997326
|
G | A | 2 | a0118a0119 | 2 | HG00741.hp2 HG03704.hp1 |
missense_variant | MODERATE | c.880C>T | p.Arg294Trp | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1048/5983 | 880/5658 | 294/1885 | chr19 | 16997326 | ||
| chr19:17000487
|
A | G | 93 | a0001a0002a0004others(90): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
missense_variant | MODERATE | c.794T>C | p.Met265Thr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/42 | 962/5983 | 794/5658 | 265/1885 | chr19 | 17000487 | ||
| chr19:17002273
|
G | A | 5 | a0047a0120a0121others(2): Show | 6 | HG02895.hp2 HG02897.hp1 HG03453.hp1 others(3): Show |
missense_variant | MODERATE | c.751C>T | p.Arg251Trp | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/42 | 919/5983 | 751/5658 | 251/1885 | chr19 | 17002273 | ||
| chr19:17008543
|
C | T | 2 | a0030a0048 | 3 | HG02145.hp2 HG02976.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.521G>A | p.Arg174Gln | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/42 | 689/5983 | 521/5658 | 174/1885 | chr19 | 17008543 | ||
| chr19:17011643
|
C | T | 1 | a0123 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.382G>A | p.Ala128Thr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 4/42 | 550/5983 | 382/5658 | 128/1885 | chr19 | 17011643 | ||
| chr19:17011732
|
G | C | 1 | a0124 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.293C>G | p.Ala98Gly | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 4/42 | 461/5983 | 293/5658 | 98/1885 | chr19 | 17011732 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16897767
|
G | C | 118 | a0001c0013a0002c0017a0002c0018others(115): Show | 160 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(157): Show |
synonymous_variant | LOW | c.4989C>G | p.Thr1663Thr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/42 | 5157/5983 | 4989/5658 | 1663/1885 | chr19 | 16897767 | ||
| chr19:16897917
|
T | A | 1 | a0012c0083 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.4926A>T | p.Pro1642Pro | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 38/42 | 5094/5983 | 4926/5658 | 1642/1885 | chr19 | 16897917 | ||
| chr19:16903606
|
C | T | 1 | a0008c0150 | 1 | HG01168.hp2 | synonymous_variant | LOW | c.4425G>A | p.Thr1475Thr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/42 | 4593/5983 | 4425/5658 | 1475/1885 | chr19 | 16903606 | ||
| chr19:16914475
|
C | T | 1 | a0002c0056 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.3810G>A | p.Pro1270Pro | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/42 | 3978/5983 | 3810/5658 | 1270/1885 | chr19 | 16914475 | ||
| chr19:16914738
|
G | A | 1 | a0004c0100 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.3705C>T | p.Ala1235Ala | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 28/42 | 3873/5983 | 3705/5658 | 1235/1885 | chr19 | 16914738 | ||
| chr19:16929154
|
G | T | 1 | a0019c0146 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.2932C>A | p.Arg978Arg | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/42 | 3100/5983 | 2932/5658 | 978/1885 | chr19 | 16929154 | ||
| chr19:16938414
|
G | A | 2 | a0002c0120a0002c0176 | 2 | HG02886.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.2826C>T | p.Ser942Ser | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/42 | 2994/5983 | 2826/5658 | 942/1885 | chr19 | 16938414 | ||
| chr19:16938420
|
G | C | 15 | a0002c0018a0016c0185a0020c0011others(12): Show | 20 | HG01361.hp1 HG01884.hp1 HG02055.hp1 others(17): Show |
synonymous_variant | LOW | c.2820C>G | p.Thr940Thr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/42 | 2988/5983 | 2820/5658 | 940/1885 | chr19 | 16938420 | ||
| chr19:16938435
|
G | A | 23 | a0002c0120a0002c0176a0005c0131others(20): Show | 25 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
synonymous_variant | LOW | c.2805C>T | p.Val935Val | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/42 | 2973/5983 | 2805/5658 | 935/1885 | chr19 | 16938435 | ||
| chr19:16938444
|
C | T | 1 | a0110c0115 | 1 | HG02055.hp2 | splice_region_variant&synonymous_variant | LOW | c.2796G>A | p.Ala932Ala | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/42 | 2964/5983 | 2796/5658 | 932/1885 | chr19 | 16938444 | ||
| chr19:16945663
|
G | A | 1 | a0035c0026 | 2 | HG01168.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.2679C>T | p.Tyr893Tyr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/42 | 2847/5983 | 2679/5658 | 893/1885 | chr19 | 16945663 | ||
| chr19:16957885
|
G | A | 1 | a0011c0090 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.2244C>T | p.Pro748Pro | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/42 | 2412/5983 | 2244/5658 | 748/1885 | chr19 | 16957885 | ||
| chr19:16970980
|
G | A | 18 | a0001c0007a0001c0102a0002c0062others(15): Show | 25 | HG00423.hp2 HG00597.hp2 HG01346.hp1 others(22): Show |
synonymous_variant | LOW | c.2124C>T | p.Asp708Asp | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/42 | 2292/5983 | 2124/5658 | 708/1885 | chr19 | 16970980 | ||
| chr19:16977413
|
G | A | 5 | a0016c0185a0028c0181a0028c0182others(2): Show | 5 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.1713C>T | p.Val571Val | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/42 | 1881/5983 | 1713/5658 | 571/1885 | chr19 | 16977413 | ||
| chr19:16980546
|
C | T | 6 | a0065c0101a0083c0112a0084c0111others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
synonymous_variant | LOW | c.1536G>A | p.Ala512Ala | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/42 | 1704/5983 | 1536/5658 | 512/1885 | chr19 | 16980546 | ||
| chr19:16980558
|
T | G | 96 | a0001c0001a0001c0007a0001c0013others(93): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
synonymous_variant | LOW | c.1524A>C | p.Arg508Arg | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/42 | 1692/5983 | 1524/5658 | 508/1885 | chr19 | 16980558 | ||
| chr19:16989742
|
A | G | 121 | a0001c0001a0001c0007a0001c0013others(118): Show | 171 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(168): Show |
synonymous_variant | LOW | c.1296T>C | p.Pro432Pro | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/42 | 1464/5983 | 1296/5658 | 432/1885 | chr19 | 16989742 | ||
| chr19:16989751
|
G | A | 1 | a0029c0137 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.1287C>T | p.Asn429Asn | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/42 | 1455/5983 | 1287/5658 | 429/1885 | chr19 | 16989751 | ||
| chr19:16993500
|
G | A | 1 | a0100c0068 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1182C>T | p.Tyr394Tyr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/42 | 1350/5983 | 1182/5658 | 394/1885 | chr19 | 16993500 | ||
| chr19:16993569
|
G | A | 3 | a0008c0160a0029c0067a0047c0046 | 4 | HG02698.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.1113C>T | p.Pro371Pro | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/42 | 1281/5983 | 1113/5658 | 371/1885 | chr19 | 16993569 | ||
| chr19:16997228
|
G | A | 1 | a0038c0109 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.978C>T | p.Asp326Asp | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1146/5983 | 978/5658 | 326/1885 | chr19 | 16997228 | ||
| chr19:16997288
|
C | T | 15 | a0016c0050a0016c0116a0016c0117others(12): Show | 15 | HG00741.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
synonymous_variant | LOW | c.918G>A | p.Ala306Ala | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1086/5983 | 918/5658 | 306/1885 | chr19 | 16997288 | ||
| chr19:16997333
|
G | A | 1 | a0100c0068 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.873C>T | p.Leu291Leu | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/42 | 1041/5983 | 873/5658 | 291/1885 | chr19 | 16997333 | ||
| chr19:17000462
|
T | C | 1 | a0040c0141 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.819A>G | p.Val273Val | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/42 | 987/5983 | 819/5658 | 273/1885 | chr19 | 17000462 | ||
| chr19:17002337
|
A | G | 48 | a0002c0017a0002c0018a0002c0019others(45): Show | 60 | HG00140.hp2 HG00642.hp1 HG01109.hp1 others(57): Show |
synonymous_variant | LOW | c.687T>C | p.Phe229Phe | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/42 | 855/5983 | 687/5658 | 229/1885 | chr19 | 17002337 | ||
| chr19:17004358
|
G | A | 1 | a0082c0165 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.588C>T | p.Ser196Ser | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/42 | 756/5983 | 588/5658 | 196/1885 | chr19 | 17004358 | ||
| chr19:17011653
|
G | A | 23 | a0002c0017a0002c0018a0002c0176others(20): Show | 29 | HG01167.hp1 HG01169.hp2 HG01928.hp2 others(26): Show |
synonymous_variant | LOW | c.372C>T | p.Asp124Asp | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 4/42 | 540/5983 | 372/5658 | 124/1885 | chr19 | 17011653 | ||
| chr19:17011749
|
C | T | 2 | a0002c0019a0088c0047 | 3 | HG02622.hp1 HG02647.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.276G>A | p.Thr92Thr | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 4/42 | 444/5983 | 276/5658 | 92/1885 | chr19 | 17011749 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16892955
|
A | C | 1 | a0022c0106t0003 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*153T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 42/42 | 153 | chr19 | 16892955 | |||||
| chr19:16892978
|
T | G | 120 | a0001c0013t0001a0002c0017t0001a0002c0018t0001others(117): Show | 161 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*130A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 42/42 | 130 | chr19 | 16892978 | |||||
| chr19:17026805
|
C | A | 1 | a0015c0008t0004 | 1 | HG00735.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-163G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/42 | chr19 | 17026805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16893388
|
G | A | 6 | a0007c0016t0001g0123a0007c0016t0001g0124a0030c0167t0001g0271others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5427-49C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16893388 | ||||||
| chr19:16893425
|
G | A | 1 | a0063c0144t0001g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5427-86C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16893425 | ||||||
| chr19:16893744
|
C | T | 1 | a0019c0146t0001g0198 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.5427-405G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16893744 | ||||||
| chr19:16893763
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5427-424G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16893763 | ||||||
| chr19:16893808
|
C | G | 4 | a0010c0004t0001g0068a0063c0144t0001g0118a0117c0110t0001g0055others(1): Show | 4 | HG03098.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.5427-469G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16893808 | ||||||
| chr19:16893841
|
G | A | 1 | a0011c0084t0001g0181 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.5427-502C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16893841 | ||||||
| chr19:16893919
|
G | A | 1 | a0002c0056t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5427-580C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16893919 | ||||||
| chr19:16893962
|
G | A | 2 | a0123c0048t0001g0011a0124c0186t0001g0049 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5427-623C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16893962 | ||||||
| chr19:16894218
|
C | T | 12 | a0002c0017t0001g0112a0002c0120t0001g0074a0020c0011t0001g0017others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.5427-879G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894218 | ||||||
| chr19:16894385
|
T | C | 1 | a0016c0117t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5427-1046A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894385 | ||||||
| chr19:16894544
|
C | T | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5427-1205G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894544 | ||||||
| chr19:16894576
|
T | A | 52 | a0007c0016t0001g0123a0007c0016t0001g0124a0008c0009t0001g0197others(49): Show | 52 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.5427-1237A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894576 | ||||||
| chr19:16894675
|
A | G | 2 | a0028c0181t0002g0060a0061c0142t0002g0015 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.5427-1336T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894675 | ||||||
| chr19:16894895
|
G | A | 6 | a0007c0016t0001g0123a0007c0016t0001g0124a0030c0167t0001g0271others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5426+1281C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894895 | ||||||
| chr19:16894921
|
A | AAC | 102 | a0001c0001t0002g0199a0001c0001t0002g0219a0001c0001t0002g0248others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.5426+1253_5426+125 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894921 | ||||||
| chr19:16894921
|
A | AACAC | 37 | a0001c0001t0002g0147a0001c0007t0002g0036a0001c0007t0002g0053others(34): Show | 37 | HG00609.hp1 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.5426+1251_5426+125 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894921 | ||||||
| chr19:16894921
|
A | AACACAC | 36 | a0001c0013t0001g0261a0002c0120t0001g0074a0004c0180t0001g0041others(33): Show | 36 | HG00735.hp1 HG01070.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.5426+1249_5426+125 others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894921 | ||||||
| chr19:16894921
|
A | AACACACA others(1): Show |
20 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0017t0001g0112others(17): Show | 20 | HG01071.hp1 HG01081.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.5426+1247_5426+125 others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894921 | ||||||
| chr19:16894921
|
A | AACACACA others(3): Show |
17 | a0002c0018t0001g0099a0002c0018t0001g0115a0002c0018t0001g0116others(14): Show | 17 | HG01168.hp1 HG01169.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.5426+1245_5426+125 others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894921 | ||||||
| chr19:16894921
|
A | AACACACA others(5): Show |
13 | a0002c0017t0001g0113a0002c0019t0001g0008a0002c0019t0001g0139others(10): Show | 13 | HG02109.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.5426+1243_5426+125 others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894921 | ||||||
| chr19:16894921
|
A | AACACACA others(7): Show |
5 | a0031c0041t0001g0253a0045c0051t0001g0083a0045c0118t0001g0024others(2): Show | 5 | HG00438.hp1 HG00597.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.5426+1241_5426+125 others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894921 | ||||||
| chr19:16894921
|
A | AACACACA others(9): Show |
5 | a0002c0017t0001g0162a0016c0116t0001g0010a0031c0041t0001g0216others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5426+1239_5426+125 others(20): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894921 | ||||||
| chr19:16894921
|
A | AACACACA others(11): Show |
2 | a0079c0085t0001g0047a0087c0178t0001g0103 | 2 | HG00609.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.5426+1237_5426+125 others(22): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894921 | ||||||
| chr19:16894921
|
AACACACA others(5): Show |
A | 6 | a0007c0016t0001g0123a0007c0016t0001g0124a0030c0167t0001g0271others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5426+1243_5426+125 others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894921 | ||||||
| chr19:16894971
|
G | A | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5426+1205C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16894971 | ||||||
| chr19:16895072
|
C | A | 2 | a0035c0026t0001g0233a0035c0026t0001g0234 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.5426+1104G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895072 | ||||||
| chr19:16895168
|
G | C | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5426+1008C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895168 | ||||||
| chr19:16895255
|
C | CA | 12 | a0002c0017t0001g0112a0002c0120t0001g0074a0020c0011t0001g0017others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.5426+920dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895255 | ||||||
| chr19:16895270
|
G | T | 2 | a0035c0026t0001g0233a0035c0026t0001g0234 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.5426+906C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895270 | ||||||
| chr19:16895299
|
G | A | 52 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(49): Show | 52 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.5426+877C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895299 | ||||||
| chr19:16895307
|
G | A | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5426+869C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895307 | ||||||
| chr19:16895322
|
A | T | 1 | a0051c0153t0001g0237 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.5426+854T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895322 | ||||||
| chr19:16895417
|
G | A | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5426+759C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895417 | ||||||
| chr19:16895589
|
A | G | 4 | a0016c0117t0001g0114a0023c0075t0001g0137a0042c0174t0001g0160others(1): Show | 4 | HG02647.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5426+587T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895589 | ||||||
| chr19:16895879
|
C | T | 1 | a0009c0042t0001g0206 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.5426+297G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895879 | ||||||
| chr19:16895884
|
T | TGC | 30 | a0001c0001t0002g0048a0001c0001t0002g0276a0002c0062t0002g0176others(27): Show | 30 | HG00423.hp1 HG00423.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.5426+290_5426+291d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895884 | ||||||
| chr19:16895886
|
C | A | 41 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(38): Show | 41 | HG00609.hp1 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.5426+290G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895886 | ||||||
| chr19:16895887
|
G | T | 1 | a0008c0160t0001g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5426+289C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895887 | ||||||
| chr19:16895889
|
G | T | 41 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(38): Show | 41 | HG00609.hp1 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.5426+287C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895889 | ||||||
| chr19:16895901
|
A | G | 6 | a0011c0090t0001g0255a0014c0077t0001g0249a0017c0044t0001g0076others(3): Show | 6 | HG02055.hp2 HG02056.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.5426+275T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895901 | ||||||
| chr19:16895903
|
G | A | 7 | a0011c0090t0001g0255a0014c0077t0001g0249a0017c0044t0001g0076others(4): Show | 7 | HG02055.hp2 HG02056.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.5426+273C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895903 | ||||||
| chr19:16895903
|
G | GCA | 25 | a0001c0001t0002g0147a0001c0001t0002g0277a0001c0013t0001g0090others(22): Show | 25 | HG00140.hp1 HG00741.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.5426+271_5426+272d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895903 | ||||||
| chr19:16895903
|
G | GCGCA | 3 | a0055c0145t0001g0093a0073c0082t0001g0069a0108c0183t0001g0056 | 3 | HG02717.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5426+272_5426+273i others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895903 | ||||||
| chr19:16895903
|
GCA | G | 47 | a0001c0013t0001g0261a0002c0017t0001g0113a0002c0018t0001g0099others(44): Show | 47 | HG00597.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.5426+271_5426+272d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895903 | ||||||
| chr19:16895903
|
GCACACA | G | 6 | a0007c0016t0001g0123a0007c0016t0001g0124a0030c0167t0001g0271others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5426+267_5426+272d others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895903 | ||||||
| chr19:16895905
|
A | G | 12 | a0011c0090t0001g0255a0014c0077t0001g0249a0017c0044t0001g0076others(9): Show | 12 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.5426+271T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895905 | ||||||
| chr19:16895907
|
A | G | 2 | a0007c0119t0001g0122a0029c0067t0001g0004 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.5426+269T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895907 | ||||||
| chr19:16895923
|
A | G | 1 | a0002c0017t0001g0112 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5426+253T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895923 | ||||||
| chr19:16895925
|
A | G | 29 | a0002c0017t0001g0112a0002c0017t0001g0162a0002c0120t0001g0074others(26): Show | 29 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.5426+251T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895925 | ||||||
| chr19:16895927
|
A | ACACACAC others(5): Show |
1 | a0063c0144t0001g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5426+248_5426+249i others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895927 | ||||||
| chr19:16895927
|
A | ACACACAC others(3): Show |
1 | a0046c0036t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5426+248_5426+249i others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895927 | ||||||
| chr19:16895927
|
A | ACACACGC others(1): Show |
7 | a0008c0009t0001g0247a0010c0004t0001g0088a0010c0004t0001g0089others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.5426+248_5426+249i others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895927 | ||||||
| chr19:16895927
|
A | ACACGCG | 21 | a0008c0009t0001g0217a0008c0150t0001g0273a0010c0004t0001g0201others(18): Show | 21 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.5426+248_5426+249i others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895927 | ||||||
| chr19:16895927
|
A | ACACGCGC others(1): Show |
4 | a0008c0009t0001g0197a0010c0004t0001g0254a0049c0154t0001g0195others(1): Show | 4 | HG01109.hp2 HG02015.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.5426+248_5426+249i others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895927 | ||||||
| chr19:16895927
|
A | ACGCGCG | 12 | a0008c0160t0001g0040a0015c0008t0001g0005a0015c0008t0001g0174others(9): Show | 12 | HG00609.hp1 HG01167.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.5426+243_5426+248d others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895927 | ||||||
| chr19:16895927
|
A | G | 99 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(96): Show | 99 | HG00597.hp2 HG00642.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.5426+249T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895927 | ||||||
| chr19:16895976
|
G | A | 43 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(40): Show | 43 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.5426+200C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16895976 | ||||||
| chr19:16896136
|
A | C | 4 | a0055c0145t0001g0093a0073c0082t0001g0069a0086c0179t0001g0102others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.5426+40T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16896136 | ||||||
| chr19:16896154
|
C | A | 1 | a0098c0172t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5426+22G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 41/41 | chr19 | 16896154 | ||||||
| chr19:16896339
|
G | A | 1 | a0109c0184t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5276-13C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 40/41 | chr19 | 16896339 | ||||||
| chr19:16896407
|
A | G | 1 | a0123c0048t0001g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5275+49T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 40/41 | chr19 | 16896407 | ||||||
| chr19:16896772
|
C | G | 1 | a0079c0085t0001g0047 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.5066-107G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16896772 | ||||||
| chr19:16896929
|
G | A | 7 | a0002c0056t0001g0081a0016c0117t0001g0114a0023c0075t0001g0137others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.5066-264C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16896929 | ||||||
| chr19:16896930
|
C | T | 1 | a0016c0185t0001g0058 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5066-265G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16896930 | ||||||
| chr19:16896990
|
A | C | 41 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(38): Show | 41 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.5066-325T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16896990 | ||||||
| chr19:16897001
|
A | C | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5066-336T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16897001 | ||||||
| chr19:16897042
|
G | C | 43 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(40): Show | 43 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.5066-377C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16897042 | ||||||
| chr19:16897062
|
A | G | 43 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(40): Show | 43 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.5066-397T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16897062 | ||||||
| chr19:16897103
|
T | C | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5066-438A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16897103 | ||||||
| chr19:16897167
|
C | T | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5066-502G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16897167 | ||||||
| chr19:16897206
|
C | T | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5065+485G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16897206 | ||||||
| chr19:16897294
|
A | T | 67 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0013t0001g0261others(64): Show | 67 | HG00597.hp2 HG00642.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.5065+397T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16897294 | ||||||
| chr19:16897394
|
A | G | 1 | a0004c0005t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.5065+297T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16897394 | ||||||
| chr19:16897568
|
C | G | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5065+123G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 39/41 | chr19 | 16897568 | ||||||
| chr19:16897810
|
C | A | 5 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0019t0001g0008others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4955-9G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 38/41 | chr19 | 16897810 | ||||||
| chr19:16897999
|
G | A | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.4849-5C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16897999 | ||||||
| chr19:16898144
|
C | CT | 39 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(36): Show | 39 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.4849-151dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898144 | ||||||
| chr19:16898144
|
C | CTT | 7 | a0010c0004t0001g0089a0010c0004t0001g0254a0025c0020t0001g0153others(4): Show | 7 | HG01109.hp2 HG01261.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.4849-152_4849-151d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898144 | ||||||
| chr19:16898186
|
C | A | 5 | a0002c0056t0001g0081a0016c0117t0001g0114a0023c0075t0001g0137others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.4849-192G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898186 | ||||||
| chr19:16898286
|
A | G | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4849-292T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898286 | ||||||
| chr19:16898295
|
C | G | 1 | a0073c0082t0001g0069 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4849-301G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898295 | ||||||
| chr19:16898346
|
A | AT | 12 | a0002c0017t0001g0112a0002c0120t0001g0074a0020c0011t0001g0017others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.4849-353dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898346 | ||||||
| chr19:16898368
|
A | G | 1 | a0073c0082t0001g0069 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4849-374T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898368 | ||||||
| chr19:16898459
|
A | G | 1 | a0006c0015t0002g0263 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4849-465T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898459 | ||||||
| chr19:16898537
|
A | G | 1 | a0011c0012t0002g0202 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.4849-543T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898537 | ||||||
| chr19:16898561
|
A | G | 66 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0013t0001g0261others(63): Show | 66 | HG00597.hp2 HG00642.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.4849-567T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898561 | ||||||
| chr19:16898691
|
A | T | 3 | a0008c0009t0001g0217a0008c0150t0001g0273a0010c0004t0001g0243 | 3 | HG01168.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.4849-697T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898691 | ||||||
| chr19:16898921
|
G | GT | 16 | a0002c0017t0001g0113a0002c0018t0001g0099a0002c0018t0001g0115others(13): Show | 16 | HG00597.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.4848+553dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898921 | ||||||
| chr19:16898921
|
G | T | 1 | a0084c0111t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4848+554C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16898921 | ||||||
| chr19:16899201
|
G | A | 1 | a0014c0105t0001g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4848+274C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16899201 | ||||||
| chr19:16899228
|
T | A | 1 | a0006c0006t0001g0205 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4848+247A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16899228 | ||||||
| chr19:16899387
|
G | T | 4 | a0002c0017t0001g0162a0016c0116t0001g0010a0048c0168t0001g0272others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4848+88C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16899387 | ||||||
| chr19:16899388
|
C | G | 2 | a0028c0181t0002g0060a0061c0142t0002g0015 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4848+87G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 37/41 | chr19 | 16899388 | ||||||
| chr19:16899573
|
G | T | 6 | a0007c0016t0001g0123a0007c0016t0001g0124a0030c0167t0001g0271others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-24C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16899573 | ||||||
| chr19:16899681
|
C | T | 1 | a0076c0088t0001g0084 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4774-132G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16899681 | ||||||
| chr19:16899781
|
C | T | 30 | a0002c0017t0001g0112a0002c0017t0001g0162a0002c0056t0001g0081others(27): Show | 30 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.4774-232G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16899781 | ||||||
| chr19:16899841
|
G | A | 1 | a0043c0022t0001g0232 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4774-292C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16899841 | ||||||
| chr19:16899847
|
C | T | 2 | a0063c0144t0001g0118a0117c0110t0001g0055 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4774-298G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16899847 | ||||||
| chr19:16899898
|
A | AT | 61 | a0002c0017t0001g0113a0002c0018t0001g0099a0002c0018t0001g0115others(58): Show | 61 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.4774-350dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16899898 | ||||||
| chr19:16899898
|
AT | A | 18 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0013t0001g0261others(15): Show | 18 | HG01099.hp2 HG01168.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.4774-350delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16899898 | ||||||
| chr19:16899998
|
C | A | 1 | a0002c0018t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4774-449G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16899998 | ||||||
| chr19:16900115
|
C | T | 52 | a0007c0016t0001g0123a0007c0016t0001g0124a0008c0009t0001g0197others(49): Show | 52 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.4774-566G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16900115 | ||||||
| chr19:16900206
|
C | G | 7 | a0002c0056t0001g0081a0016c0117t0001g0114a0023c0075t0001g0137others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4774-657G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16900206 | ||||||
| chr19:16900320
|
C | G | 43 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(40): Show | 43 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.4774-771G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16900320 | ||||||
| chr19:16900382
|
G | A | 22 | a0002c0017t0001g0112a0002c0017t0001g0162a0002c0120t0001g0074others(19): Show | 22 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.4773+828C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16900382 | ||||||
| chr19:16900436
|
C | A | 44 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(41): Show | 44 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.4773+774G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16900436 | ||||||
| chr19:16900471
|
G | C | 1 | a0119c0140t0002g0111 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4773+739C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16900471 | ||||||
| chr19:16900599
|
T | G | 1 | a0003c0151t0001g0143 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4773+611A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16900599 | ||||||
| chr19:16900674
|
T | C | 54 | a0007c0016t0001g0123a0007c0016t0001g0124a0008c0009t0001g0197others(51): Show | 54 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.4773+536A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16900674 | ||||||
| chr19:16900754
|
G | A | 41 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(38): Show | 41 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.4773+456C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16900754 | ||||||
| chr19:16901006
|
C | A | 3 | a0027c0035t0001g0045a0039c0076t0001g0126a0083c0112t0001g0096 | 3 | HG01081.hp2 HG01975.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.4773+204G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16901006 | ||||||
| chr19:16901049
|
G | T | 41 | a0008c0009t0001g0197a0008c0009t0001g0217a0008c0009t0001g0231others(38): Show | 41 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.4773+161C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16901049 | ||||||
| chr19:16901074
|
A | G | 1 | a0038c0099t0002g0224 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.4773+136T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16901074 | ||||||
| chr19:16901106
|
A | G | 2 | a0063c0144t0001g0118a0117c0110t0001g0055 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4773+104T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16901106 | ||||||
| chr19:16901166
|
G | A | 2 | a0030c0167t0001g0271a0034c0071t0001g0070 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4773+44C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 36/41 | chr19 | 16901166 | ||||||
| chr19:16901547
|
A | G | 13 | a0007c0016t0001g0123a0007c0016t0001g0124a0010c0004t0001g0068others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.4686-250T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16901547 | ||||||
| chr19:16901573
|
C | T | 1 | a0001c0102t0002g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4686-276G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16901573 | ||||||
| chr19:16901799
|
T | C | 1 | a0113c0136t0002g0169 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.4686-502A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16901799 | ||||||
| chr19:16901847
|
G | A | 8 | a0001c0001t0002g0277a0001c0033t0002g0027a0002c0058t0002g0149others(5): Show | 8 | HG00099.hp2 HG01099.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.4686-550C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16901847 | ||||||
| chr19:16901911
|
T | C | 2 | a0063c0144t0001g0118a0117c0110t0001g0055 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4686-614A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16901911 | ||||||
| chr19:16901946
|
C | CG | 26 | a0001c0007t0002g0221a0002c0017t0001g0113a0005c0003t0002g0051others(23): Show | 26 | HG00741.hp2 HG01099.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.4686-650dupC | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16901946 | ||||||
| chr19:16902013
|
G | A | 2 | a0017c0147t0001g0009a0069c0098t0001g0065 | 2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4685+636C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902013 | ||||||
| chr19:16902053
|
G | T | 2 | a0063c0144t0001g0118a0117c0110t0001g0055 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4685+596C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902053 | ||||||
| chr19:16902140
|
C | T | 1 | a0098c0172t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4685+509G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902140 | ||||||
| chr19:16902242
|
C | T | 1 | a0020c0011t0001g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4685+407G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902242 | ||||||
| chr19:16902252
|
C | G | 8 | a0001c0001t0002g0048a0003c0002t0002g0196a0003c0045t0002g0052others(5): Show | 8 | HG01978.hp2 HG02148.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.4685+397G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902252 | ||||||
| chr19:16902312
|
C | T | 2 | a0028c0181t0002g0060a0061c0142t0002g0015 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4685+337G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902312 | ||||||
| chr19:16902324
|
G | A | 4 | a0002c0017t0001g0162a0016c0116t0001g0010a0048c0168t0001g0272others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4685+325C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902324 | ||||||
| chr19:16902379
|
T | C | 2 | a0017c0147t0001g0009a0069c0098t0001g0065 | 2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4685+270A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902379 | ||||||
| chr19:16902391
|
C | A | 1 | a0001c0001t0002g0248 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4685+258G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902391 | ||||||
| chr19:16902562
|
G | A | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4685+87C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902562 | ||||||
| chr19:16902573
|
C | T | 1 | a0073c0082t0001g0069 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4685+76G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902573 | ||||||
| chr19:16902628
|
C | T | 1 | a0020c0011t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4685+21G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 35/41 | chr19 | 16902628 | ||||||
| chr19:16902900
|
G | T | 1 | a0025c0169t0001g0120 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4471-37C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16902900 | ||||||
| chr19:16902901
|
G | A | 1 | a0004c0014t0002g0222 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4471-38C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16902901 | ||||||
| chr19:16903006
|
G | A | 1 | a0113c0136t0002g0169 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.4471-143C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16903006 | ||||||
| chr19:16903109
|
C | T | 73 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0013t0001g0261others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.4471-246G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16903109 | ||||||
| chr19:16903289
|
C | T | 1 | a0079c0085t0001g0047 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4470+272G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16903289 | ||||||
| chr19:16903366
|
TGGGGGTG others(12): Show |
T | 14 | a0007c0016t0001g0123a0007c0016t0001g0124a0010c0004t0001g0068others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4470+176_4470+194d others(21): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16903366 | ||||||
| chr19:16903387
|
G | C | 1 | a0014c0105t0001g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4470+174C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16903387 | ||||||
| chr19:16903506
|
G | A | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4470+55C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16903506 | ||||||
| chr19:16903508
|
A | T | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4470+53T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16903508 | ||||||
| chr19:16903509
|
T | G | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4470+52A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16903509 | ||||||
| chr19:16903551
|
A | C | 3 | a0063c0144t0001g0118a0098c0172t0001g0006a0117c0110t0001g0055 | 3 | HG02965.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4470+10T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 34/41 | chr19 | 16903551 | ||||||
| chr19:16903670
|
A | C | 1 | a0098c0172t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4407+32T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 33/41 | chr19 | 16903670 | ||||||
| chr19:16903877
|
C | T | 1 | a0003c0002t0002g0213 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4252-20G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 32/41 | chr19 | 16903877 | ||||||
| chr19:16903887
|
C | A | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4252-30G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 32/41 | chr19 | 16903887 | ||||||
| chr19:16903908
|
T | C | 2 | a0025c0169t0001g0120a0037c0104t0001g0150 | 2 | HG00639.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.4252-51A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 32/41 | chr19 | 16903908 | ||||||
| chr19:16903932
|
A | C | 4 | a0055c0145t0001g0093a0073c0082t0001g0069a0086c0179t0001g0102others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4252-75T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 32/41 | chr19 | 16903932 | ||||||
| chr19:16903956
|
C | T | 10 | a0002c0176t0001g0014a0010c0004t0001g0068a0029c0067t0001g0004others(7): Show | 10 | HG00438.hp1 HG00597.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.4252-99G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 32/41 | chr19 | 16903956 | ||||||
| chr19:16903961
|
C | T | 4 | a0002c0017t0001g0162a0016c0116t0001g0010a0048c0168t0001g0272others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4252-104G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 32/41 | chr19 | 16903961 | ||||||
| chr19:16904061
|
G | A | 169 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0013t0001g0261others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.4251+165C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 32/41 | chr19 | 16904061 | ||||||
| chr19:16904209
|
G | T | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4251+17C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 32/41 | chr19 | 16904209 | ||||||
| chr19:16904581
|
T | C | 1 | a0054c0159t0001g0128 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4028-29A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16904581 | ||||||
| chr19:16904610
|
C | G | 18 | a0002c0176t0001g0014a0007c0016t0001g0123a0007c0016t0001g0124others(15): Show | 18 | HG00438.hp1 HG00597.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.4028-58G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16904610 | ||||||
| chr19:16904618
|
G | A | 92 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0017t0001g0112others(89): Show | 92 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.4028-66C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16904618 | ||||||
| chr19:16904654
|
G | A | 1 | a0001c0001t0002g0185 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4028-102C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16904654 | ||||||
| chr19:16904689
|
G | A | 11 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0019t0001g0008others(8): Show | 11 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.4028-137C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16904689 | ||||||
| chr19:16904797
|
T | C | 120 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0013t0001g0261others(117): Show | 120 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.4028-245A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16904797 | ||||||
| chr19:16904875
|
C | T | 84 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(81): Show | 84 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.4028-323G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16904875 | ||||||
| chr19:16904950
|
A | C | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4028-398T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16904950 | ||||||
| chr19:16904958
|
T | A | 3 | a0023c0075t0001g0137a0042c0174t0001g0160a0088c0047t0001g0161 | 3 | HG02647.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4028-406A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16904958 | ||||||
| chr19:16904990
|
G | A | 95 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0017t0001g0112others(92): Show | 95 | HG00609.hp1 HG00639.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.4028-438C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16904990 | ||||||
| chr19:16905133
|
C | A | 1 | a0063c0144t0001g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4028-581G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905133 | ||||||
| chr19:16905317
|
T | C | 123 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0013t0001g0261others(120): Show | 123 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.4028-765A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905317 | ||||||
| chr19:16905378
|
G | C | 4 | a0014c0027t0001g0175a0014c0077t0001g0249a0096c0061t0001g0168others(1): Show | 4 | HG00597.hp2 HG02083.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.4028-826C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905378 | ||||||
| chr19:16905540
|
C | CA | 9 | a0001c0001t0002g0199a0002c0062t0002g0176a0003c0002t0002g0105others(6): Show | 9 | HG01934.hp2 HG02083.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.4028-989dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905540 | ||||||
| chr19:16905540
|
CA | C | 43 | a0001c0001t0002g0248a0001c0001t0002g0276a0001c0013t0001g0261others(40): Show | 43 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.4028-989delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905540 | ||||||
| chr19:16905540
|
CAA | C | 77 | a0002c0017t0001g0112a0002c0017t0001g0162a0002c0018t0001g0099others(74): Show | 77 | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.4028-990_4028-989d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905540 | ||||||
| chr19:16905540
|
CAAAAAAA others(22): Show |
C | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4028-1017_4028-989 others(32): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905540 | ||||||
| chr19:16905545
|
AAAAAAAA others(17): Show |
A | 3 | a0027c0035t0001g0045a0039c0076t0001g0126a0083c0112t0001g0096 | 3 | HG01081.hp2 HG01975.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.4028-1017_4028-994 others(27): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905545 | ||||||
| chr19:16905567
|
A | T | 1 | a0077c0087t0001g0225 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4028-1015T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905567 | ||||||
| chr19:16905569
|
G | GA | 16 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0017t0001g0113others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.4028-1018dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905569 | ||||||
| chr19:16905569
|
GA | G | 66 | a0001c0001t0002g0185a0002c0017t0001g0112a0002c0059t0001g0044others(63): Show | 66 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.4028-1018delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905569 | ||||||
| chr19:16905703
|
T | C | 1 | a0034c0071t0001g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4028-1151A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905703 | ||||||
| chr19:16905725
|
A | G | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4028-1173T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905725 | ||||||
| chr19:16905764
|
C | A | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4027+1188G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905764 | ||||||
| chr19:16905824
|
T | A | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4027+1128A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905824 | ||||||
| chr19:16905840
|
T | C | 1 | a0063c0144t0001g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4027+1112A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16905840 | ||||||
| chr19:16906005
|
CT | C | 8 | a0006c0015t0002g0110a0006c0132t0002g0087a0009c0010t0002g0078others(5): Show | 8 | HG01346.hp1 HG01433.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.4027+946delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906005 | ||||||
| chr19:16906043
|
G | A | 1 | a0080c0089t0002g0250 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4027+909C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906043 | ||||||
| chr19:16906052
|
G | A | 2 | a0063c0144t0001g0118a0117c0110t0001g0055 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4027+900C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906052 | ||||||
| chr19:16906098
|
T | C | 1 | a0025c0020t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4027+854A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906098 | ||||||
| chr19:16906104
|
T | C | 2 | a0006c0015t0002g0263a0113c0136t0002g0169 | 2 | HG03490.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4027+848A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906104 | ||||||
| chr19:16906136
|
T | G | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4027+816A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906136 | ||||||
| chr19:16906191
|
C | T | 1 | a0009c0042t0001g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4027+761G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906191 | ||||||
| chr19:16906200
|
A | C | 1 | a0123c0048t0001g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4027+752T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906200 | ||||||
| chr19:16906289
|
C | G | 8 | a0002c0018t0001g0099a0002c0018t0001g0115a0002c0018t0001g0116others(5): Show | 8 | HG02486.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4027+663G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906289 | ||||||
| chr19:16906300
|
CCTCT | C | 4 | a0055c0145t0001g0093a0073c0082t0001g0069a0086c0179t0001g0102others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4027+648_4027+651d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906300 | ||||||
| chr19:16906304
|
T | C | 3 | a0001c0013t0001g0261a0003c0151t0001g0143a0012c0083t0001g0132 | 3 | HG01099.hp2 HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.4027+648A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906304 | ||||||
| chr19:16906337
|
C | CCTTT | 17 | a0001c0001t0002g0147a0001c0001t0002g0266a0003c0045t0002g0052others(14): Show | 17 | HG01109.hp1 HG01975.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.4027+611_4027+614d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
C | CCTTTCTT others(1): Show |
9 | a0001c0007t0002g0221a0001c0033t0002g0002a0003c0002t0002g0105others(6): Show | 9 | HG00741.hp1 HG01433.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.4027+607_4027+614d others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
C | CCTTTCTT others(5): Show |
2 | a0068c0095t0002g0064a0103c0129t0001g0129 | 2 | HG04228.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.4027+603_4027+614d others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
C | CCTTTCTT others(9): Show |
1 | a0004c0014t0002g0222 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4027+599_4027+614d others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
C | CTTTCTTT others(12): Show |
1 | a0003c0002t0002g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4027+614_4027+615i others(21): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
CCTTT | C | 29 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0013t0001g0261others(26): Show | 29 | HG00099.hp2 HG00597.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.4027+611_4027+614d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
CCTTTCTT others(1): Show |
C | 22 | a0001c0001t0002g0185a0001c0001t0002g0219a0001c0013t0001g0138others(19): Show | 22 | HG00423.hp2 HG01099.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.4027+607_4027+614d others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
CCTTTCTT others(5): Show |
C | 16 | a0003c0002t0002g0186a0003c0002t0002g0200a0004c0005t0002g0188others(13): Show | 16 | HG00438.hp1 HG01099.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.4027+603_4027+614d others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
CCTTTCTT others(9): Show |
C | 9 | a0002c0059t0001g0044a0002c0176t0001g0014a0003c0002t0002g0252others(6): Show | 9 | HG00423.hp1 HG01081.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.4027+599_4027+614d others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
CCTTTCTT others(13): Show |
C | 19 | a0001c0001t0002g0048a0001c0013t0001g0090a0006c0006t0001g0131others(16): Show | 19 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.4027+595_4027+614d others(22): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
CCTTTCTT others(17): Show |
C | 13 | a0006c0006t0001g0220a0006c0015t0002g0263a0009c0010t0002g0208others(10): Show | 13 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4027+591_4027+614d others(26): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
CCTTTCTT others(21): Show |
C | 4 | a0024c0030t0001g0148a0046c0036t0001g0031a0112c0135t0002g0268others(1): Show | 4 | HG00639.hp2 HG03490.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4027+587_4027+614d others(30): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906337
|
CCTTTCTT others(29): Show |
C | 1 | a0011c0090t0001g0255 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4027+579_4027+614d others(38): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906337 | ||||||
| chr19:16906346
|
CTTTCTTT others(3): Show |
C | 1 | a0059c0156t0002g0259 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.4027+596_4027+605d others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906346 | ||||||
| chr19:16906348
|
TTCTTTCT others(3): Show |
T | 1 | a0002c0017t0001g0112 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4027+594_4027+603d others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906348 | ||||||
| chr19:16906348
|
TTCTTTCT others(7): Show |
T | 1 | a0093c0177t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4027+590_4027+603d others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906348 | ||||||
| chr19:16906348
|
TTCTTTCT others(11): Show |
T | 3 | a0020c0011t0001g0017a0020c0011t0001g0021a0021c0143t0001g0012 | 3 | HG02055.hp1 HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4027+586_4027+603d others(20): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906348 | ||||||
| chr19:16906351
|
TTTCTTTC others(8): Show |
T | 1 | a0099c0054t0001g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4027+586_4027+600d others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906351 | ||||||
| chr19:16906366
|
CTTTCTTT others(4): Show |
C | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4027+575_4027+585d others(13): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906366 | ||||||
| chr19:16906370
|
CTTTCTTT others(4): Show |
C | 2 | a0002c0017t0001g0113a0007c0016t0001g0007 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.4027+571_4027+581d others(13): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906370 | ||||||
| chr19:16906383
|
T | C | 1 | a0106c0134t0001g0109 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4027+569A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906383 | ||||||
| chr19:16906383
|
T | TTTCCTTC others(9): Show |
2 | a0035c0026t0001g0233a0035c0026t0001g0234 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4027+568_4027+569i others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906383 | ||||||
| chr19:16906383
|
TTTCTTTC others(21): Show |
T | 1 | a0003c0002t0002g0092 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4027+541_4027+568d others(30): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906383 | ||||||
| chr19:16906387
|
T | C | 10 | a0006c0006t0001g0086a0006c0006t0001g0205a0009c0042t0001g0206others(7): Show | 10 | HG01081.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.4027+565A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906387 | ||||||
| chr19:16906387
|
TTTCTTTC others(17): Show |
T | 2 | a0010c0004t0001g0201a0025c0020t0001g0153 | 2 | HG01934.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.4027+541_4027+564d others(26): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906387 | ||||||
| chr19:16906391
|
T | C | 37 | a0002c0059t0001g0044a0006c0006t0001g0086a0006c0006t0001g0131others(34): Show | 37 | HG00597.hp2 HG00609.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.4027+561A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906391 | ||||||
| chr19:16906391
|
T | TTTCCTTC others(5): Show |
1 | a0063c0144t0001g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4027+560_4027+561i others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906391 | ||||||
| chr19:16906391
|
T | TTTCCTTC others(9): Show |
1 | a0026c0127t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4027+560_4027+561i others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906391 | ||||||
| chr19:16906391
|
TTTCTTTC others(13): Show |
T | 1 | a0027c0035t0001g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4027+541_4027+560d others(22): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906391 | ||||||
| chr19:16906395
|
T | C | 52 | a0002c0059t0001g0044a0003c0151t0001g0143a0006c0006t0001g0086others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.4027+557A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906395 | ||||||
| chr19:16906395
|
TTTCTTTC others(9): Show |
T | 7 | a0008c0009t0001g0217a0010c0004t0001g0243a0037c0104t0001g0150others(4): Show | 7 | HG00639.hp1 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.4027+541_4027+556d others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906395 | ||||||
| chr19:16906399
|
T | C | 59 | a0001c0013t0001g0090a0001c0013t0001g0261a0002c0019t0001g0139others(56): Show | 59 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4027+553A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906399 | ||||||
| chr19:16906399
|
TTTCTTTC others(5): Show |
T | 9 | a0002c0056t0001g0081a0008c0009t0001g0231a0010c0004t0001g0088others(6): Show | 9 | HG00438.hp2 HG00741.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.4027+541_4027+552d others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906399 | ||||||
| chr19:16906400
|
T | C | 1 | a0055c0145t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4027+552A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906400 | ||||||
| chr19:16906403
|
T | A | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4027+549A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906403 | ||||||
| chr19:16906403
|
T | C | 60 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0013t0001g0261others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.4027+549A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906403 | ||||||
| chr19:16906403
|
T | TTTCCTTC others(5): Show |
4 | a0002c0019t0001g0008a0007c0016t0001g0123a0007c0016t0001g0124others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4027+548_4027+549i others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906403 | ||||||
| chr19:16906403
|
TTTCTTTC others(1): Show |
T | 18 | a0002c0018t0001g0115a0002c0018t0001g0116a0010c0004t0001g0089others(15): Show | 18 | HG00609.hp1 HG00735.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.4027+541_4027+548d others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906403 | ||||||
| chr19:16906404
|
T | C | 1 | a0124c0186t0001g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4027+548A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906404 | ||||||
| chr19:16906407
|
T | C | 83 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0013t0001g0261others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.4027+545A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906407
|
T | TTTCC | 4 | a0001c0102t0002g0079a0005c0003t0002g0236a0012c0028t0002g0177others(1): Show | 4 | HG02148.hp2 HG02293.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4027+541_4027+544d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906407
|
T | TTTCCTTC others(5): Show |
2 | a0081c0079t0001g0080a0122c0162t0001g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4027+533_4027+544d others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906407
|
T | TTTCCTTC others(9): Show |
1 | a0098c0172t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4027+529_4027+544d others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906407
|
T | TTTCTTTC others(1): Show |
3 | a0001c0001t0002g0199a0003c0002t0002g0196a0005c0003t0002g0166 | 3 | HG01361.hp2 HG01978.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.4027+544_4027+545i others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906407
|
T | TTTCTTTC others(5): Show |
1 | a0108c0183t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4027+544_4027+545i others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906407
|
T | TTTCTTTC others(9): Show |
2 | a0010c0004t0001g0068a0042c0175t0001g0075 | 2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4027+544_4027+545i others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906407
|
T | TTTCTTTC others(9): Show |
1 | a0034c0071t0001g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4027+544_4027+545i others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906407
|
T | TTTCTTTC others(9): Show |
1 | a0061c0142t0002g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4027+544_4027+545i others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906407
|
T | TTTCTTTC others(13): Show |
1 | a0102c0130t0002g0030 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.4027+544_4027+545i others(22): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906407
|
TTTCC | T | 15 | a0001c0007t0002g0053a0002c0018t0001g0099a0004c0005t0002g0046others(12): Show | 15 | HG01071.hp1 HG01071.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.4027+541_4027+544d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906407 | ||||||
| chr19:16906410
|
C | CTTTCTTT others(3): Show |
1 | a0026c0034t0002g0032 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4027+541_4027+542i others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906410 | ||||||
| chr19:16906411
|
C | T | 19 | a0002c0017t0001g0112a0002c0017t0001g0162a0002c0120t0001g0074others(16): Show | 19 | HG01070.hp1 HG01070.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.4027+541G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906411 | ||||||
| chr19:16906414
|
C | T | 1 | a0028c0114t0001g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4027+538G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906414 | ||||||
| chr19:16906415
|
C | T | 2 | a0016c0185t0001g0058a0104c0133t0002g0241 | 2 | HG02135.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.4027+537G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906415 | ||||||
| chr19:16906529
|
G | A | 1 | a0002c0176t0001g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4027+423C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906529 | ||||||
| chr19:16906537
|
G | A | 4 | a0055c0145t0001g0093a0073c0082t0001g0069a0086c0179t0001g0102others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4027+415C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906537 | ||||||
| chr19:16906598
|
T | C | 1 | a0003c0002t0002g0252 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4027+354A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906598 | ||||||
| chr19:16906606
|
A | G | 212 | a0001c0001t0002g0147a0001c0001t0002g0219a0001c0001t0002g0248others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.4027+346T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906606 | ||||||
| chr19:16906802
|
C | G | 1 | a0099c0054t0001g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4027+150G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906802 | ||||||
| chr19:16906887
|
G | A | 1 | a0001c0013t0001g0261 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4027+65C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 30/41 | chr19 | 16906887 | ||||||
| chr19:16907281
|
C | G | 8 | a0012c0029t0001g0151a0012c0029t0001g0152a0026c0127t0001g0240others(5): Show | 8 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.3862-164G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907281 | ||||||
| chr19:16907307
|
C | CT | 170 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0199others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.3862-191dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907307 | ||||||
| chr19:16907307
|
C | CTT | 49 | a0001c0013t0001g0261a0002c0056t0001g0081a0002c0058t0002g0149others(46): Show | 49 | HG00423.hp1 HG00735.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.3862-192_3862-191d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907307 | ||||||
| chr19:16907307
|
CT | C | 5 | a0001c0001t0002g0266a0055c0145t0001g0093a0073c0082t0001g0069others(2): Show | 5 | HG01884.hp1 HG02300.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3862-191delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907307 | ||||||
| chr19:16907381
|
G | A | 6 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0019t0001g0008others(3): Show | 6 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3862-264C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907381 | ||||||
| chr19:16907606
|
C | CA | 106 | a0001c0001t0002g0147a0001c0001t0002g0219a0001c0001t0002g0276others(103): Show | 106 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.3862-490dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907606 | ||||||
| chr19:16907606
|
C | CAA | 21 | a0001c0007t0002g0036a0002c0120t0001g0074a0004c0180t0001g0041others(18): Show | 21 | HG01071.hp1 HG01071.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.3862-491_3862-490d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907606 | ||||||
| chr19:16907606
|
CA | C | 16 | a0001c0013t0001g0261a0003c0151t0001g0143a0007c0170t0002g0117others(13): Show | 16 | HG01099.hp2 HG01192.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.3862-490delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907606 | ||||||
| chr19:16907606
|
CAA | C | 53 | a0006c0006t0001g0086a0006c0006t0001g0131a0006c0006t0001g0183others(50): Show | 53 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.3862-491_3862-490d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907606 | ||||||
| chr19:16907670
|
C | T | 1 | a0006c0015t0002g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3862-553G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907670 | ||||||
| chr19:16907794
|
A | G | 8 | a0007c0052t0002g0119a0007c0170t0002g0117a0034c0070t0002g0091others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3862-677T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907794 | ||||||
| chr19:16907815
|
C | T | 11 | a0001c0001t0002g0048a0003c0002t0002g0092a0003c0002t0002g0196others(8): Show | 11 | HG00423.hp2 HG00438.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.3862-698G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16907815 | ||||||
| chr19:16908042
|
C | T | 142 | a0001c0001t0002g0147a0001c0001t0002g0219a0001c0001t0002g0248others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.3862-925G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16908042 | ||||||
| chr19:16908362
|
TA | T | 254 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0199others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.3862-1246delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16908362 | ||||||
| chr19:16908362
|
TAA | T | 8 | a0008c0009t0001g0247a0009c0010t0002g0208a0009c0010t0002g0209others(5): Show | 8 | HG01071.hp1 HG01071.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.3862-1247_3862-124 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16908362 | ||||||
| chr19:16908376
|
AT | A | 3 | a0001c0013t0001g0261a0003c0151t0001g0143a0012c0083t0001g0132 | 3 | HG01099.hp2 HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.3862-1260delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16908376 | ||||||
| chr19:16908412
|
C | T | 2 | a0052c0152t0002g0029a0070c0096t0002g0251 | 2 | NA18963.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.3862-1295G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16908412 | ||||||
| chr19:16908821
|
G | C | 1 | a0002c0176t0001g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3862-1704C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16908821 | ||||||
| chr19:16908980
|
C | T | 140 | a0001c0001t0002g0147a0001c0001t0002g0219a0001c0001t0002g0248others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.3862-1863G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16908980 | ||||||
| chr19:16909082
|
C | T | 2 | a0001c0001t0002g0219a0003c0002t0002g0105 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3862-1965G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909082 | ||||||
| chr19:16909083
|
A | T | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3862-1966T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909083 | ||||||
| chr19:16909097
|
G | A | 142 | a0001c0001t0002g0147a0001c0001t0002g0219a0001c0001t0002g0248others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.3862-1980C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909097 | ||||||
| chr19:16909134
|
G | A | 1 | a0070c0096t0002g0251 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3862-2017C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909134 | ||||||
| chr19:16909222
|
G | A | 5 | a0001c0013t0001g0261a0012c0083t0001g0132a0055c0145t0001g0093others(2): Show | 5 | HG01099.hp2 HG01192.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3862-2105C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909222 | ||||||
| chr19:16909255
|
T | A | 2 | a0002c0176t0001g0014a0107c0122t0001g0023 | 2 | HG01361.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3862-2138A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909255 | ||||||
| chr19:16909300
|
T | A | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3862-2183A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909300 | ||||||
| chr19:16909340
|
C | T | 1 | a0041c0023t0002g0157 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3862-2223G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909340 | ||||||
| chr19:16909417
|
G | A | 1 | a0039c0107t0001g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3862-2300C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909417 | ||||||
| chr19:16909493
|
G | A | 1 | a0036c0025t0002g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3862-2376C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909493 | ||||||
| chr19:16909537
|
C | T | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3862-2420G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909537 | ||||||
| chr19:16909551
|
G | A | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3862-2434C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909551 | ||||||
| chr19:16909552
|
A | G | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3862-2435T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909552 | ||||||
| chr19:16909740
|
G | A | 8 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0019t0001g0008others(5): Show | 8 | HG01361.hp1 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3862-2623C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909740 | ||||||
| chr19:16909744
|
C | CA | 162 | a0001c0001t0002g0147a0001c0001t0002g0219a0001c0001t0002g0248others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.3862-2628dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909744 | ||||||
| chr19:16909852
|
G | A | 27 | a0001c0001t0002g0248a0001c0001t0002g0276a0001c0001t0002g0277others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(24): Show |
intron_variant | MODIFIER | c.3862-2735C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909852 | ||||||
| chr19:16909878
|
A | G | 166 | a0001c0001t0002g0147a0001c0001t0002g0219a0001c0001t0002g0248others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.3862-2761T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909878 | ||||||
| chr19:16909965
|
C | T | 1 | a0002c0059t0001g0044 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3862-2848G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909965 | ||||||
| chr19:16909998
|
C | T | 72 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0019t0001g0008others(69): Show | 72 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3862-2881G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16909998 | ||||||
| chr19:16910072
|
G | A | 5 | a0002c0056t0001g0081a0016c0117t0001g0114a0023c0075t0001g0137others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3862-2955C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910072 | ||||||
| chr19:16910081
|
G | A | 5 | a0004c0005t0002g0211a0005c0003t0002g0167a0013c0049t0002g0170others(2): Show | 5 | HG02040.hp1 HG03669.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.3862-2964C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910081 | ||||||
| chr19:16910219
|
G | C | 1 | a0025c0020t0001g0153 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3862-3102C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910219 | ||||||
| chr19:16910231
|
G | A | 5 | a0001c0013t0001g0261a0012c0083t0001g0132a0055c0145t0001g0093others(2): Show | 5 | HG01099.hp2 HG01192.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3862-3114C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910231 | ||||||
| chr19:16910256
|
G | A | 143 | a0001c0001t0002g0147a0001c0001t0002g0219a0001c0001t0002g0248others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.3862-3139C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910256 | ||||||
| chr19:16910382
|
C | G | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3862-3265G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910382 | ||||||
| chr19:16910408
|
G | A | 1 | a0083c0112t0001g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3862-3291C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910408 | ||||||
| chr19:16910418
|
C | T | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3862-3301G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910418 | ||||||
| chr19:16910451
|
G | A | 1 | a0073c0082t0001g0069 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3862-3334C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910451 | ||||||
| chr19:16910455
|
C | G | 1 | a0013c0049t0002g0170 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3862-3338G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910455 | ||||||
| chr19:16910466
|
G | A | 1 | a0007c0170t0002g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3862-3349C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910466 | ||||||
| chr19:16910466
|
G | C | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3862-3349C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910466 | ||||||
| chr19:16910467
|
C | G | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3862-3350G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910467 | ||||||
| chr19:16910468
|
CT | C | 254 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.3862-3352delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910468 | ||||||
| chr19:16910469
|
T | C | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3862-3352A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910469 | ||||||
| chr19:16910806
|
G | A | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3861+3618C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910806 | ||||||
| chr19:16910988
|
T | C | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3861+3436A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910988 | ||||||
| chr19:16910989
|
C | T | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3861+3435G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16910989 | ||||||
| chr19:16911013
|
G | C | 1 | a0093c0177t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3861+3411C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16911013 | ||||||
| chr19:16911076
|
G | A | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3861+3348C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16911076 | ||||||
| chr19:16911124
|
C | T | 3 | a0005c0003t0002g0244a0013c0078t0002g0171a0038c0109t0002g0165 | 3 | HG00423.hp2 HG04184.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3861+3300G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16911124 | ||||||
| chr19:16911125
|
G | A | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3861+3299C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16911125 | ||||||
| chr19:16911142
|
C | T | 4 | a0004c0005t0002g0211a0013c0049t0002g0170a0068c0095t0002g0064others(1): Show | 4 | HG03669.hp1 NA18992.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.3861+3282G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16911142 | ||||||
| chr19:16911236
|
G | A | 1 | a0009c0042t0001g0206 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3861+3188C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16911236 | ||||||
| chr19:16911379
|
T | C | 1 | a0039c0107t0001g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3861+3045A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16911379 | ||||||
| chr19:16911510
|
C | T | 1 | a0008c0009t0001g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3861+2914G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16911510 | ||||||
| chr19:16911671
|
G | A | 2 | a0005c0121t0002g0267a0060c0157t0002g0142 | 2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.3861+2753C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16911671 | ||||||
| chr19:16911761
|
G | A | 7 | a0007c0119t0001g0122a0056c0072t0001g0094a0065c0101t0001g0001others(4): Show | 7 | HG02486.hp2 HG02886.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3861+2663C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16911761 | ||||||
| chr19:16912040
|
C | T | 1 | a0006c0006t0001g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3861+2384G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16912040 | ||||||
| chr19:16912296
|
A | G | 2 | a0045c0118t0001g0024a0101c0126t0001g0061 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3861+2128T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16912296 | ||||||
| chr19:16912538
|
C | A | 4 | a0001c0013t0001g0261a0012c0083t0001g0132a0073c0082t0001g0069others(1): Show | 4 | HG01099.hp2 HG01192.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.3861+1886G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16912538 | ||||||
| chr19:16912595
|
G | A | 6 | a0002c0056t0001g0081a0016c0117t0001g0114a0023c0075t0001g0137others(3): Show | 6 | HG02647.hp2 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3861+1829C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16912595 | ||||||
| chr19:16912646
|
G | A | 1 | a0011c0012t0002g0207 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3861+1778C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16912646 | ||||||
| chr19:16912735
|
C | T | 1 | a0001c0007t0002g0053 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3861+1689G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16912735 | ||||||
| chr19:16912771
|
C | T | 1 | a0124c0186t0001g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3861+1653G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16912771 | ||||||
| chr19:16913206
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3861+1218C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913206 | ||||||
| chr19:16913259
|
A | T | 4 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0019t0001g0008others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3861+1165T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913259 | ||||||
| chr19:16913346
|
G | T | 8 | a0001c0001t0002g0277a0001c0033t0002g0027a0002c0058t0002g0149others(5): Show | 8 | HG00099.hp2 HG01099.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.3861+1078C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913346 | ||||||
| chr19:16913451
|
G | A | 7 | a0007c0119t0001g0122a0056c0072t0001g0094a0065c0101t0001g0001others(4): Show | 7 | HG02486.hp2 HG02886.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3861+973C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913451 | ||||||
| chr19:16913451
|
G | GCCATGTG others(40): Show |
1 | a0001c0001t0002g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3861+926_3861+972d others(49): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913451 | ||||||
| chr19:16913652
|
A | G | 3 | a0001c0013t0001g0261a0003c0151t0001g0143a0012c0083t0001g0132 | 3 | HG01099.hp2 HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.3861+772T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913652 | ||||||
| chr19:16913723
|
T | C | 40 | a0001c0001t0002g0248a0001c0001t0002g0276a0001c0001t0002g0277others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.3861+701A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913723 | ||||||
| chr19:16913822
|
A | G | 1 | a0040c0074t0002g0212 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3861+602T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913822 | ||||||
| chr19:16913843
|
G | A | 2 | a0091c0055t0001g0121a0117c0110t0001g0055 | 2 | HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3861+581C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913843 | ||||||
| chr19:16913862
|
G | T | 44 | a0001c0001t0002g0248a0001c0001t0002g0276a0001c0001t0002g0277others(41): Show | 44 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.3861+562C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913862 | ||||||
| chr19:16913974
|
G | A | 1 | a0026c0127t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3861+450C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16913974 | ||||||
| chr19:16914254
|
AAG | A | 4 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0019t0001g0008others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3861+168_3861+169d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16914254 | ||||||
| chr19:16914257
|
A | G | 4 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0019t0001g0008others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3861+167T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 29/41 | chr19 | 16914257 | ||||||
| chr19:16914501
|
G | A | 43 | a0002c0018t0001g0099a0002c0018t0001g0115a0002c0018t0001g0116others(40): Show | 43 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(40): Show |
splice_region_variant&intron_variant | LOW | c.3787-3C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 28/41 | chr19 | 16914501 | ||||||
| chr19:16914839
|
A | T | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3630-26T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16914839 | ||||||
| chr19:16914954
|
C | G | 1 | a0051c0153t0001g0237 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3630-141G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16914954 | ||||||
| chr19:16915015
|
C | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3630-202G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915015 | ||||||
| chr19:16915175
|
G | GTCCT | 7 | a0002c0120t0001g0074a0020c0011t0001g0017a0020c0011t0001g0021others(4): Show | 7 | HG01361.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3630-366_3630-363d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915175 | ||||||
| chr19:16915265
|
C | A | 1 | a0026c0127t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3630-452G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915265 | ||||||
| chr19:16915631
|
G | T | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3630-818C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915631 | ||||||
| chr19:16915638
|
C | T | 122 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(119): Show | 122 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.3630-825G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915638 | ||||||
| chr19:16915810
|
C | A | 117 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(114): Show | 117 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.3630-997G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915810 | ||||||
| chr19:16915822
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3630-1009A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915822 | ||||||
| chr19:16915827
|
GCCTT | G | 121 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(118): Show | 121 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.3630-1018_3630-101 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915827 | ||||||
| chr19:16915831
|
T | G | 1 | a0001c0001t0002g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3630-1018A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915831 | ||||||
| chr19:16915885
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3630-1072A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915885 | ||||||
| chr19:16915890
|
TTTTC | T | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3630-1081_3630-107 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16915890 | ||||||
| chr19:16916130
|
C | A | 119 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(116): Show | 119 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.3630-1317G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916130 | ||||||
| chr19:16916161
|
G | A | 1 | a0006c0006t0001g0220 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3630-1348C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916161 | ||||||
| chr19:16916220
|
C | T | 1 | a0004c0005t0002g0042 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3630-1407G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916220 | ||||||
| chr19:16916233
|
C | T | 1 | a0005c0003t0002g0236 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3630-1420G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916233 | ||||||
| chr19:16916251
|
T | C | 119 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(116): Show | 119 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.3630-1438A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916251 | ||||||
| chr19:16916385
|
G | A | 4 | a0056c0072t0001g0094a0072c0081t0001g0067a0092c0173t0001g0164others(1): Show | 4 | HG02486.hp2 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3630-1572C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916385 | ||||||
| chr19:16916579
|
A | G | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3630-1766T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916579 | ||||||
| chr19:16916580
|
T | TA | 7 | a0023c0031t0001g0025a0023c0031t0001g0026a0023c0075t0001g0137others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3630-1768dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916580 | ||||||
| chr19:16916625
|
G | C | 2 | a0001c0001t0002g0158a0001c0001t0002g0185 | 2 | NA18971.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.3630-1812C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916625 | ||||||
| chr19:16916632
|
G | A | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3630-1819C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916632 | ||||||
| chr19:16916669
|
G | T | 1 | a0001c0001t0002g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3630-1856C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916669 | ||||||
| chr19:16916797
|
A | G | 119 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(116): Show | 119 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.3630-1984T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916797 | ||||||
| chr19:16916892
|
G | T | 2 | a0032c0043t0001g0191a0046c0036t0001g0031 | 2 | NA18965.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.3630-2079C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916892 | ||||||
| chr19:16916937
|
G | A | 6 | a0017c0147t0001g0009a0028c0114t0001g0100a0028c0181t0002g0060others(3): Show | 6 | HG02647.hp1 HG03195.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3630-2124C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16916937 | ||||||
| chr19:16917024
|
G | A | 3 | a0006c0006t0001g0183a0014c0105t0001g0140a0060c0157t0002g0142 | 3 | HG02602.hp1 HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.3630-2211C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917024 | ||||||
| chr19:16917063
|
C | G | 1 | a0004c0005t0002g0042 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3630-2250G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917063 | ||||||
| chr19:16917180
|
C | T | 2 | a0008c0009t0001g0197a0040c0074t0002g0212 | 2 | HG02015.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.3630-2367G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917180 | ||||||
| chr19:16917397
|
T | A | 2 | a0003c0151t0001g0143a0044c0021t0002g0269 | 2 | HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.3630-2584A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917397 | ||||||
| chr19:16917459
|
G | A | 4 | a0002c0056t0001g0081a0002c0176t0001g0014a0016c0117t0001g0114others(1): Show | 4 | HG01361.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3630-2646C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917459 | ||||||
| chr19:16917470
|
G | A | 118 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(115): Show | 118 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.3630-2657C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917470 | ||||||
| chr19:16917695
|
T | G | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3630-2882A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917695 | ||||||
| chr19:16917734
|
T | C | 1 | a0007c0016t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3630-2921A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917734 | ||||||
| chr19:16917861
|
C | T | 1 | a0089c0065t0002g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3630-3048G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917861 | ||||||
| chr19:16917886
|
G | A | 1 | a0025c0020t0001g0153 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3630-3073C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917886 | ||||||
| chr19:16917939
|
G | A | 1 | a0081c0079t0001g0080 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3630-3126C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16917939 | ||||||
| chr19:16918056
|
C | T | 120 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(117): Show | 120 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.3630-3243G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918056 | ||||||
| chr19:16918084
|
C | CTCCA | 4 | a0019c0039t0001g0227a0019c0039t0001g0238a0039c0107t0001g0184others(1): Show | 4 | HG00642.hp1 HG01978.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.3630-3275_3630-327 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918084 | ||||||
| chr19:16918330
|
A | C | 2 | a0027c0035t0001g0045a0039c0076t0001g0126 | 2 | HG01081.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.3630-3517T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918330 | ||||||
| chr19:16918418
|
TG | T | 120 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(117): Show | 120 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.3629+3486delC | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918418 | ||||||
| chr19:16918428
|
T | A | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3629+3477A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918428 | ||||||
| chr19:16918430
|
G | A | 9 | a0001c0013t0001g0138a0007c0052t0002g0119a0007c0170t0002g0117others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.3629+3475C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918430 | ||||||
| chr19:16918441
|
ACTT | A | 3 | a0036c0025t0002g0189a0103c0129t0001g0129a0118c0139t0001g0108 | 3 | HG00741.hp2 HG04228.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.3629+3461_3629+346 others(7): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918441 | ||||||
| chr19:16918441
|
ACTTT | A | 115 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(112): Show | 115 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.3629+3460_3629+346 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918441 | ||||||
| chr19:16918442
|
C | CT | 37 | a0002c0056t0001g0081a0003c0002t0002g0154a0010c0004t0001g0068others(34): Show | 37 | HG00438.hp1 HG00735.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.3629+3462dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918442 | ||||||
| chr19:16918442
|
CT | C | 6 | a0001c0001t0002g0048a0003c0002t0002g0092a0021c0037t0002g0256others(3): Show | 6 | HG00438.hp2 HG02056.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.3629+3462delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918442 | ||||||
| chr19:16918463
|
T | A | 120 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(117): Show | 120 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.3629+3442A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918463 | ||||||
| chr19:16918529
|
C | G | 1 | a0026c0127t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3629+3376G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918529 | ||||||
| chr19:16918604
|
G | A | 42 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(39): Show | 42 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.3629+3301C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918604 | ||||||
| chr19:16918747
|
C | CT | 10 | a0001c0033t0002g0027a0002c0056t0001g0081a0002c0062t0002g0176others(7): Show | 10 | HG00099.hp2 HG01361.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.3629+3157dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918747 | ||||||
| chr19:16918747
|
CT | C | 28 | a0001c0001t0002g0048a0005c0003t0002g0125a0007c0119t0001g0122others(25): Show | 28 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3629+3157delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918747 | ||||||
| chr19:16918747
|
CTT | C | 14 | a0003c0002t0002g0105a0003c0002t0002g0186a0003c0002t0002g0200others(11): Show | 14 | HG00438.hp1 HG02056.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.3629+3156_3629+315 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918747 | ||||||
| chr19:16918747
|
CTTT | C | 117 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(114): Show | 117 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.3629+3155_3629+315 others(7): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918747 | ||||||
| chr19:16918780
|
G | A | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3629+3125C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918780 | ||||||
| chr19:16918858
|
A | G | 5 | a0002c0056t0001g0081a0002c0176t0001g0014a0016c0117t0001g0114others(2): Show | 5 | HG01361.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3629+3047T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918858 | ||||||
| chr19:16918928
|
C | A | 4 | a0002c0056t0001g0081a0002c0176t0001g0014a0016c0117t0001g0114others(1): Show | 4 | HG01361.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3629+2977G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16918928 | ||||||
| chr19:16919042
|
A | C | 1 | a0003c0002t0002g0186 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3629+2863T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919042 | ||||||
| chr19:16919079
|
T | C | 1 | a0059c0156t0002g0259 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3629+2826A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919079 | ||||||
| chr19:16919152
|
G | A | 1 | a0101c0126t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3629+2753C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919152 | ||||||
| chr19:16919210
|
GA | G | 119 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(116): Show | 119 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.3629+2694delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919210 | ||||||
| chr19:16919221
|
A | G | 1 | a0003c0002t0002g0186 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3629+2684T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919221 | ||||||
| chr19:16919401
|
G | A | 1 | a0085c0063t0001g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3629+2504C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919401 | ||||||
| chr19:16919402
|
GCCT | G | 5 | a0002c0056t0001g0081a0002c0176t0001g0014a0016c0117t0001g0114others(2): Show | 5 | HG01361.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3629+2500_3629+250 others(7): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919402 | ||||||
| chr19:16919426
|
G | A | 1 | a0103c0129t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3629+2479C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919426 | ||||||
| chr19:16919696
|
G | A | 95 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(92): Show | 95 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.3629+2209C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919696 | ||||||
| chr19:16919701
|
C | T | 2 | a0063c0144t0001g0118a0124c0186t0001g0049 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3629+2204G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919701 | ||||||
| chr19:16919716
|
CA | C | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3629+2188delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919716 | ||||||
| chr19:16919739
|
A | T | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3629+2166T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919739 | ||||||
| chr19:16919783
|
G | A | 120 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(117): Show | 120 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.3629+2122C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919783 | ||||||
| chr19:16919858
|
A | C | 194 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(191): Show | 194 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.3629+2047T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919858 | ||||||
| chr19:16919901
|
T | C | 1 | a0057c0073t0001g0066 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3629+2004A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919901 | ||||||
| chr19:16919921
|
C | G | 1 | a0001c0001t0002g0276 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3629+1984G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919921 | ||||||
| chr19:16919948
|
G | A | 6 | a0023c0031t0001g0025a0023c0031t0001g0026a0023c0075t0001g0137others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3629+1957C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919948 | ||||||
| chr19:16919984
|
C | T | 11 | a0017c0044t0001g0076a0017c0044t0001g0077a0045c0051t0001g0083others(8): Show | 11 | HG00438.hp1 HG02056.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.3629+1921G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16919984 | ||||||
| chr19:16920104
|
C | T | 1 | a0002c0120t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3629+1801G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920104 | ||||||
| chr19:16920251
|
G | A | 1 | a0003c0045t0002g0052 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3629+1654C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920251 | ||||||
| chr19:16920295
|
C | T | 8 | a0017c0044t0001g0076a0017c0044t0001g0077a0050c0148t0002g0235others(5): Show | 8 | HG00438.hp1 HG02056.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.3629+1610G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920295 | ||||||
| chr19:16920314
|
T | C | 4 | a0002c0056t0001g0081a0002c0176t0001g0014a0016c0117t0001g0114others(1): Show | 4 | HG01361.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3629+1591A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920314 | ||||||
| chr19:16920372
|
C | T | 3 | a0002c0062t0002g0176a0005c0003t0002g0244a0059c0156t0002g0259 | 3 | HG01934.hp2 HG04184.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.3629+1533G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920372 | ||||||
| chr19:16920466
|
C | T | 4 | a0002c0056t0001g0081a0002c0176t0001g0014a0016c0117t0001g0114others(1): Show | 4 | HG01361.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3629+1439G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920466 | ||||||
| chr19:16920467
|
G | A | 1 | a0011c0090t0001g0255 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3629+1438C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920467 | ||||||
| chr19:16920577
|
C | T | 114 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(111): Show | 114 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.3629+1328G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920577 | ||||||
| chr19:16920593
|
C | T | 119 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(116): Show | 119 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.3629+1312G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920593 | ||||||
| chr19:16920596
|
C | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3629+1309G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920596 | ||||||
| chr19:16920620
|
C | T | 1 | a0016c0117t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3629+1285G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920620 | ||||||
| chr19:16920637
|
T | C | 119 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(116): Show | 119 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.3629+1268A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920637 | ||||||
| chr19:16920720
|
A | G | 134 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(131): Show | 134 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.3629+1185T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920720 | ||||||
| chr19:16920855
|
C | CA | 27 | a0001c0001t0002g0048a0001c0001t0002g0219a0002c0017t0001g0112others(24): Show | 27 | HG00438.hp1 HG01361.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.3629+1049dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920855 | ||||||
| chr19:16920855
|
CA | C | 8 | a0005c0003t0002g0125a0012c0029t0001g0151a0029c0137t0002g0270others(5): Show | 8 | HG01168.hp1 HG01169.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.3629+1049delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920855 | ||||||
| chr19:16920855
|
CAAAAAAA others(5): Show |
C | 119 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(116): Show | 119 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.3629+1038_3629+104 others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920855 | ||||||
| chr19:16920991
|
G | A | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3629+914C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16920991 | ||||||
| chr19:16921015
|
C | T | 118 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(115): Show | 118 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.3629+890G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921015 | ||||||
| chr19:16921027
|
C | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0185 | 2 | NA18971.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.3629+878G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921027 | ||||||
| chr19:16921031
|
C | T | 118 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(115): Show | 118 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.3629+874G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921031 | ||||||
| chr19:16921044
|
C | A | 118 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(115): Show | 118 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.3629+861G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921044 | ||||||
| chr19:16921190
|
C | T | 1 | a0066c0103t0002g0022 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3629+715G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921190 | ||||||
| chr19:16921398
|
A | C | 1 | a0093c0177t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3629+507T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921398 | ||||||
| chr19:16921450
|
C | T | 25 | a0001c0007t0002g0036a0001c0007t0002g0053a0002c0062t0002g0176others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.3629+455G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921450 | ||||||
| chr19:16921458
|
T | A | 122 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(119): Show | 122 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.3629+447A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921458 | ||||||
| chr19:16921464
|
C | T | 7 | a0002c0018t0001g0099a0002c0018t0001g0115a0002c0018t0001g0116others(4): Show | 7 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3629+441G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921464 | ||||||
| chr19:16921505
|
C | G | 122 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(119): Show | 122 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.3629+400G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921505 | ||||||
| chr19:16921682
|
ACAG | A | 131 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(128): Show | 131 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.3629+220_3629+222d others(5): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921682 | ||||||
| chr19:16921740
|
A | G | 131 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(128): Show | 131 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.3629+165T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921740 | ||||||
| chr19:16921749
|
T | C | 131 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(128): Show | 131 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.3629+156A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921749 | ||||||
| chr19:16921863
|
C | T | 1 | a0091c0055t0001g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3629+42G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 27/41 | chr19 | 16921863 | ||||||
| chr19:16921999
|
C | A | 1 | a0044c0021t0002g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3548-13G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16921999 | ||||||
| chr19:16922076
|
C | A | 1 | a0020c0011t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3548-90G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922076 | ||||||
| chr19:16922159
|
T | C | 138 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(135): Show | 138 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.3548-173A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922159 | ||||||
| chr19:16922319
|
T | C | 1 | a0103c0129t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3548-333A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922319 | ||||||
| chr19:16922344
|
A | G | 15 | a0004c0180t0001g0041a0010c0004t0001g0068a0029c0067t0001g0004others(12): Show | 15 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.3548-358T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922344 | ||||||
| chr19:16922373
|
G | A | 1 | a0007c0170t0002g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3548-387C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922373 | ||||||
| chr19:16922393
|
G | A | 2 | a0008c0009t0001g0197a0040c0074t0002g0212 | 2 | HG02015.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.3548-407C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922393 | ||||||
| chr19:16922541
|
G | C | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3548-555C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922541 | ||||||
| chr19:16922560
|
T | C | 163 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(160): Show | 163 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.3548-574A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922560 | ||||||
| chr19:16922648
|
G | A | 5 | a0002c0056t0001g0081a0002c0176t0001g0014a0016c0117t0001g0114others(2): Show | 5 | HG01361.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3548-662C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922648 | ||||||
| chr19:16922935
|
C | T | 21 | a0002c0056t0001g0081a0002c0176t0001g0014a0004c0180t0001g0041others(18): Show | 21 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.3548-949G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922935 | ||||||
| chr19:16922962
|
C | T | 10 | a0017c0044t0001g0076a0017c0044t0001g0077a0050c0148t0002g0235others(7): Show | 10 | HG00438.hp1 HG02056.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.3548-976G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16922962 | ||||||
| chr19:16923006
|
G | A | 3 | a0004c0005t0002g0188a0080c0089t0002g0250a0096c0061t0001g0168 | 3 | HG02155.hp1 HG02155.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.3548-1020C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923006 | ||||||
| chr19:16923069
|
A | G | 1 | a0002c0176t0001g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3548-1083T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923069 | ||||||
| chr19:16923132
|
T | C | 15 | a0004c0180t0001g0041a0010c0004t0001g0068a0029c0067t0001g0004others(12): Show | 15 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.3548-1146A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923132 | ||||||
| chr19:16923330
|
C | T | 1 | a0025c0020t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3548-1344G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923330 | ||||||
| chr19:16923348
|
G | A | 1 | a0007c0053t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3548-1362C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923348 | ||||||
| chr19:16923356
|
C | A | 1 | a0069c0098t0001g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3548-1370G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923356 | ||||||
| chr19:16923425
|
G | T | 1 | a0027c0035t0001g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3548-1439C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923425 | ||||||
| chr19:16923440
|
G | A | 1 | a0010c0004t0001g0201 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3548-1454C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923440 | ||||||
| chr19:16923440
|
G | T | 1 | a0027c0035t0001g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3548-1454C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923440 | ||||||
| chr19:16923449
|
C | T | 123 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(120): Show | 123 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.3548-1463G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923449 | ||||||
| chr19:16923538
|
T | C | 1 | a0055c0145t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3548-1552A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923538 | ||||||
| chr19:16923579
|
T | C | 2 | a0004c0014t0002g0223a0004c0100t0002g0054 | 2 | HG02083.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.3548-1593A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923579 | ||||||
| chr19:16923737
|
G | C | 1 | a0075c0108t0001g0141 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3547+1459C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923737 | ||||||
| chr19:16923753
|
C | T | 1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3547+1443G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923753 | ||||||
| chr19:16923756
|
G | C | 2 | a0007c0016t0001g0007a0021c0143t0001g0012 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3547+1440C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923756 | ||||||
| chr19:16923925
|
C | T | 1 | a0060c0157t0002g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3547+1271G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923925 | ||||||
| chr19:16923959
|
C | A | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3547+1237G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923959 | ||||||
| chr19:16923959
|
C | CA | 8 | a0017c0044t0001g0076a0017c0044t0001g0077a0050c0148t0002g0235others(5): Show | 8 | HG02056.hp1 HG02132.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.3547+1236dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923959 | ||||||
| chr19:16923976
|
A | C | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3547+1220T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16923976 | ||||||
| chr19:16924125
|
A | G | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3547+1071T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924125 | ||||||
| chr19:16924163
|
A | G | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3547+1033T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924163 | ||||||
| chr19:16924206
|
C | T | 1 | a0009c0042t0001g0206 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3547+990G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924206 | ||||||
| chr19:16924224
|
T | C | 45 | a0002c0056t0001g0081a0002c0176t0001g0014a0004c0180t0001g0041others(42): Show | 45 | HG00438.hp1 HG00735.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.3547+972A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924224 | ||||||
| chr19:16924243
|
G | GTGGGTAG others(3): Show |
1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+952_3547+953i others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924243 | ||||||
| chr19:16924245
|
A | G | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+951T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924245 | ||||||
| chr19:16924252
|
T | A | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+944A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924252 | ||||||
| chr19:16924261
|
G | T | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+935C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924261 | ||||||
| chr19:16924266
|
A | G | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+930T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924266 | ||||||
| chr19:16924267
|
G | T | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+929C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924267 | ||||||
| chr19:16924269
|
T | A | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+927A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924269 | ||||||
| chr19:16924303
|
A | C | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+893T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924303 | ||||||
| chr19:16924304
|
C | G | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+892G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924304 | ||||||
| chr19:16924305
|
T | C | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+891A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924305 | ||||||
| chr19:16924306
|
G | T | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+890C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924306 | ||||||
| chr19:16924307
|
C | T | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+889G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924307 | ||||||
| chr19:16924371
|
A | C | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3547+825T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924371 | ||||||
| chr19:16924607
|
G | T | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3547+589C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924607 | ||||||
| chr19:16924609
|
C | T | 1 | a0110c0115t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3547+587G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924609 | ||||||
| chr19:16924615
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3547+581G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924615 | ||||||
| chr19:16924695
|
C | T | 1 | a0021c0143t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3547+501G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924695 | ||||||
| chr19:16924739
|
T | C | 44 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(41): Show | 44 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.3547+457A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924739 | ||||||
| chr19:16924757
|
T | A | 1 | a0039c0076t0001g0126 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3547+439A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924757 | ||||||
| chr19:16924837
|
G | A | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3547+359C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924837 | ||||||
| chr19:16924941
|
T | TA | 45 | a0002c0056t0001g0081a0002c0176t0001g0014a0007c0119t0001g0122others(42): Show | 45 | HG00438.hp1 HG00735.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.3547+254dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924941 | ||||||
| chr19:16924965
|
A | G | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3547+231T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16924965 | ||||||
| chr19:16925015
|
A | C | 1 | a0002c0056t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3547+181T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16925015 | ||||||
| chr19:16925032
|
G | C | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3547+164C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16925032 | ||||||
| chr19:16925088
|
C | A | 25 | a0001c0007t0002g0036a0001c0007t0002g0053a0002c0062t0002g0176others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.3547+108G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16925088 | ||||||
| chr19:16925097
|
C | T | 2 | a0056c0072t0001g0094a0092c0173t0001g0164 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3547+99G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 26/41 | chr19 | 16925097 | ||||||
| chr19:16925436
|
C | T | 6 | a0030c0166t0002g0059a0030c0167t0001g0271a0035c0026t0001g0233others(3): Show | 6 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.3371-64G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16925436 | ||||||
| chr19:16925441
|
C | A | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3371-69G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16925441 | ||||||
| chr19:16925585
|
T | C | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3371-213A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16925585 | ||||||
| chr19:16925758
|
A | AT | 15 | a0002c0056t0001g0081a0002c0176t0001g0014a0010c0004t0001g0068others(12): Show | 15 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.3371-387dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16925758 | ||||||
| chr19:16925758
|
AT | A | 99 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(96): Show | 99 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.3371-387delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16925758 | ||||||
| chr19:16925786
|
C | G | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3371-414G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16925786 | ||||||
| chr19:16925899
|
G | A | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3371-527C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16925899 | ||||||
| chr19:16925951
|
G | C | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3371-579C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16925951 | ||||||
| chr19:16925961
|
A | C | 30 | a0007c0119t0001g0122a0016c0050t0001g0095a0017c0044t0001g0076others(27): Show | 30 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.3371-589T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16925961 | ||||||
| chr19:16925996
|
G | C | 96 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(93): Show | 96 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.3371-624C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16925996 | ||||||
| chr19:16926029
|
G | A | 27 | a0001c0007t0002g0036a0001c0007t0002g0053a0002c0062t0002g0176others(24): Show | 27 | HG00438.hp2 HG00597.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.3371-657C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926029 | ||||||
| chr19:16926270
|
C | A | 40 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(37): Show | 40 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.3371-898G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926270 | ||||||
| chr19:16926304
|
C | CTTTATTT others(3): Show |
4 | a0002c0176t0001g0014a0016c0117t0001g0114a0029c0067t0001g0004others(1): Show | 4 | HG01361.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3371-942_3371-933d others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926304 | ||||||
| chr19:16926304
|
C | CTTTATTT others(8): Show |
11 | a0002c0056t0001g0081a0016c0050t0001g0095a0030c0166t0002g0059others(8): Show | 11 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.3371-947_3371-933d others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926304 | ||||||
| chr19:16926304
|
C | CTTTATTT others(13): Show |
10 | a0007c0119t0001g0122a0010c0004t0001g0068a0028c0114t0001g0100others(7): Show | 10 | HG02257.hp1 HG02886.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.3371-952_3371-933d others(22): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926304 | ||||||
| chr19:16926304
|
C | CTTTATTT others(18): Show |
5 | a0017c0147t0001g0009a0028c0182t0001g0062a0088c0047t0001g0161others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.3371-957_3371-933d others(27): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926304 | ||||||
| chr19:16926304
|
C | CTTTATTT others(23): Show |
2 | a0050c0148t0002g0235a0100c0068t0002g0159 | 2 | HG01891.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.3371-933_3371-932i others(32): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926304 | ||||||
| chr19:16926304
|
C | CTTTATTT others(28): Show |
11 | a0017c0044t0001g0076a0017c0044t0001g0077a0023c0075t0001g0137others(8): Show | 11 | HG00438.hp1 HG02056.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.3371-933_3371-932i others(37): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926304 | ||||||
| chr19:16926304
|
C | CTTTATTT others(33): Show |
2 | a0023c0031t0001g0025a0023c0031t0001g0026 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3371-933_3371-932i others(42): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926304 | ||||||
| chr19:16926474
|
C | T | 4 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3371-1102G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926474 | ||||||
| chr19:16926560
|
C | A | 1 | a0022c0106t0003g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3371-1188G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926560 | ||||||
| chr19:16926607
|
C | T | 30 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(27): Show | 30 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.3371-1235G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926607 | ||||||
| chr19:16926637
|
C | T | 1 | a0025c0020t0001g0153 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3371-1265G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926637 | ||||||
| chr19:16926767
|
G | A | 1 | a0110c0115t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3370+1242C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926767 | ||||||
| chr19:16926805
|
G | T | 14 | a0002c0056t0001g0081a0002c0176t0001g0014a0010c0004t0001g0068others(11): Show | 14 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.3370+1204C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926805 | ||||||
| chr19:16926920
|
C | T | 1 | a0009c0010t0002g0257 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3370+1089G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926920 | ||||||
| chr19:16926954
|
C | T | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3370+1055G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16926954 | ||||||
| chr19:16927006
|
C | T | 1 | a0053c0149t0001g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3370+1003G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927006 | ||||||
| chr19:16927030
|
A | G | 32 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(29): Show | 32 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.3370+979T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927030 | ||||||
| chr19:16927140
|
T | C | 31 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(28): Show | 31 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.3370+869A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927140 | ||||||
| chr19:16927141
|
G | C | 12 | a0004c0180t0001g0041a0023c0031t0001g0025a0023c0031t0001g0026others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3370+868C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927141 | ||||||
| chr19:16927234
|
C | T | 1 | a0103c0129t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3370+775G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927234 | ||||||
| chr19:16927355
|
G | A | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3370+654C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927355 | ||||||
| chr19:16927398
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3370+611G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927398 | ||||||
| chr19:16927473
|
T | C | 2 | a0014c0105t0001g0140a0103c0129t0001g0129 | 2 | HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3370+536A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927473 | ||||||
| chr19:16927749
|
G | T | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3370+260C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927749 | ||||||
| chr19:16927752
|
G | A | 1 | a0002c0176t0001g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3370+257C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927752 | ||||||
| chr19:16927888
|
G | A | 1 | a0009c0042t0001g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3370+121C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927888 | ||||||
| chr19:16927960
|
C | T | 1 | a0115c0123t0001g0226 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3370+49G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927960 | ||||||
| chr19:16927975
|
G | A | 1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3370+34C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 25/41 | chr19 | 16927975 | ||||||
| chr19:16928249
|
C | A | 1 | a0016c0117t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3145-15G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928249 | ||||||
| chr19:16928263
|
G | A | 9 | a0002c0018t0001g0099a0002c0018t0001g0115a0002c0018t0001g0116others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.3145-29C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928263 | ||||||
| chr19:16928510
|
C | T | 1 | a0108c0183t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3145-276G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928510 | ||||||
| chr19:16928525
|
T | G | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3145-291A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928525 | ||||||
| chr19:16928535
|
C | T | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3145-301G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928535 | ||||||
| chr19:16928632
|
A | G | 1 | a0007c0016t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3144+310T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928632 | ||||||
| chr19:16928769
|
G | GT | 32 | a0002c0056t0001g0081a0002c0176t0001g0014a0003c0002t0002g0200others(29): Show | 32 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.3144+172dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928769 | ||||||
| chr19:16928769
|
G | GTT | 5 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072others(2): Show | 5 | HG01361.hp1 HG02055.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3144+171_3144+172d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928769 | ||||||
| chr19:16928812
|
C | T | 4 | a0004c0180t0001g0041a0056c0072t0001g0094a0072c0081t0001g0067others(1): Show | 4 | HG03098.hp1 HG03579.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.3144+130G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928812 | ||||||
| chr19:16928814
|
T | G | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3144+128A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928814 | ||||||
| chr19:16928825
|
T | C | 23 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3144+117A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928825 | ||||||
| chr19:16928853
|
T | C | 24 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(21): Show | 24 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.3144+89A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928853 | ||||||
| chr19:16928884
|
G | C | 1 | a0110c0115t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3144+58C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928884 | ||||||
| chr19:16928888
|
G | A | 23 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3144+54C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928888 | ||||||
| chr19:16928923
|
A | C | 1 | a0093c0177t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3144+19T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 24/41 | chr19 | 16928923 | ||||||
| chr19:16929284
|
G | A | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2846-44C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16929284 | ||||||
| chr19:16929436
|
A | G | 23 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2846-196T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16929436 | ||||||
| chr19:16929494
|
C | A | 7 | a0017c0044t0001g0076a0017c0044t0001g0077a0050c0148t0002g0235others(4): Show | 7 | HG00438.hp1 HG02056.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.2846-254G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16929494 | ||||||
| chr19:16929530
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2846-290G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16929530 | ||||||
| chr19:16929595
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2846-355C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16929595 | ||||||
| chr19:16929615
|
G | A | 1 | a0003c0045t0002g0052 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2846-375C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16929615 | ||||||
| chr19:16929830
|
G | C | 1 | a0002c0120t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2846-590C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16929830 | ||||||
| chr19:16929966
|
G | T | 23 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2846-726C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16929966 | ||||||
| chr19:16930060
|
A | G | 38 | a0002c0056t0001g0081a0002c0176t0001g0014a0004c0180t0001g0041others(35): Show | 38 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.2846-820T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930060 | ||||||
| chr19:16930125
|
G | A | 23 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2846-885C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930125 | ||||||
| chr19:16930140
|
G | A | 23 | a0007c0119t0001g0122a0016c0050t0001g0095a0017c0147t0001g0009others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2846-900C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930140 | ||||||
| chr19:16930160
|
T | C | 35 | a0002c0056t0001g0081a0002c0176t0001g0014a0004c0180t0001g0041others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.2846-920A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930160 | ||||||
| chr19:16930178
|
C | T | 23 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2846-938G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930178 | ||||||
| chr19:16930197
|
G | GT | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2846-958dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930197 | ||||||
| chr19:16930255
|
C | CA | 13 | a0017c0147t0001g0009a0023c0031t0001g0025a0023c0031t0001g0026others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2846-1016dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930255 | ||||||
| chr19:16930362
|
G | A | 26 | a0001c0007t0002g0036a0001c0007t0002g0053a0002c0062t0002g0176others(23): Show | 26 | HG00438.hp2 HG00597.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.2846-1122C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930362 | ||||||
| chr19:16930433
|
C | CAAA | 38 | a0002c0056t0001g0081a0002c0176t0001g0014a0004c0180t0001g0041others(35): Show | 38 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.2846-1194_2846-119 others(7): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930433 | ||||||
| chr19:16930439
|
A | C | 1 | a0041c0023t0002g0157 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2846-1199T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930439 | ||||||
| chr19:16930557
|
G | A | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2846-1317C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930557 | ||||||
| chr19:16930637
|
C | T | 1 | a0005c0003t0002g0125 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2846-1397G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930637 | ||||||
| chr19:16930801
|
G | A | 95 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(92): Show | 95 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2846-1561C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930801 | ||||||
| chr19:16930806
|
G | A | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2846-1566C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16930806 | ||||||
| chr19:16931036
|
C | T | 1 | a0046c0036t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2846-1796G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931036 | ||||||
| chr19:16931038
|
G | A | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2846-1798C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931038 | ||||||
| chr19:16931166
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2846-1926G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931166 | ||||||
| chr19:16931172
|
A | C | 23 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2846-1932T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931172 | ||||||
| chr19:16931221
|
C | A | 1 | a0016c0117t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2846-1981G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931221 | ||||||
| chr19:16931245
|
G | A | 22 | a0007c0119t0001g0122a0016c0050t0001g0095a0017c0147t0001g0009others(19): Show | 22 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2846-2005C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931245 | ||||||
| chr19:16931322
|
C | T | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2846-2082G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931322 | ||||||
| chr19:16931326
|
C | T | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2846-2086G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931326 | ||||||
| chr19:16931352
|
T | C | 38 | a0002c0056t0001g0081a0002c0176t0001g0014a0004c0180t0001g0041others(35): Show | 38 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.2846-2112A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931352 | ||||||
| chr19:16931445
|
A | G | 1 | a0002c0176t0001g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2846-2205T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931445 | ||||||
| chr19:16931545
|
G | T | 9 | a0002c0018t0001g0099a0002c0018t0001g0115a0002c0018t0001g0116others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2846-2305C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931545 | ||||||
| chr19:16931553
|
G | T | 4 | a0028c0114t0001g0100a0028c0181t0002g0060a0028c0182t0001g0062others(1): Show | 4 | HG02647.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2846-2313C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931553 | ||||||
| chr19:16931755
|
C | G | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2846-2515G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931755 | ||||||
| chr19:16931803
|
C | A | 1 | a0002c0120t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2846-2563G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931803 | ||||||
| chr19:16931850
|
C | T | 1 | a0038c0099t0002g0224 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2846-2610G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931850 | ||||||
| chr19:16931870
|
A | G | 13 | a0004c0180t0001g0041a0023c0031t0001g0025a0023c0031t0001g0026others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2846-2630T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931870 | ||||||
| chr19:16931969
|
G | A | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2846-2729C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16931969 | ||||||
| chr19:16932000
|
G | A | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2846-2760C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932000 | ||||||
| chr19:16932087
|
A | G | 1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2846-2847T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932087 | ||||||
| chr19:16932090
|
T | G | 3 | a0002c0017t0001g0112a0002c0017t0001g0113a0108c0183t0001g0056 | 3 | HG02615.hp1 HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2846-2850A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932090 | ||||||
| chr19:16932096
|
TA | T | 14 | a0004c0180t0001g0041a0023c0031t0001g0025a0023c0031t0001g0026others(11): Show | 14 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2846-2857delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932096 | ||||||
| chr19:16932231
|
G | A | 23 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2846-2991C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932231 | ||||||
| chr19:16932406
|
G | A | 7 | a0017c0147t0001g0009a0028c0114t0001g0100a0028c0181t0002g0060others(4): Show | 7 | HG02055.hp2 HG02647.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2846-3166C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932406 | ||||||
| chr19:16932563
|
A | AAATAC | 38 | a0002c0056t0001g0081a0002c0176t0001g0014a0004c0180t0001g0041others(35): Show | 38 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.2846-3324_2846-332 others(9): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932563 | ||||||
| chr19:16932599
|
A | C | 23 | a0004c0180t0001g0041a0007c0119t0001g0122a0016c0050t0001g0095others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2846-3359T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932599 | ||||||
| chr19:16932650
|
AC | A | 14 | a0002c0056t0001g0081a0002c0176t0001g0014a0010c0004t0001g0068others(11): Show | 14 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2846-3411delG | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932650 | ||||||
| chr19:16932844
|
A | C | 1 | a0014c0027t0001g0180 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2846-3604T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932844 | ||||||
| chr19:16932874
|
G | A | 1 | a0003c0002t0002g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2846-3634C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932874 | ||||||
| chr19:16932924
|
A | G | 1 | a0049c0154t0001g0195 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2846-3684T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16932924 | ||||||
| chr19:16933039
|
T | C | 35 | a0002c0056t0001g0081a0002c0176t0001g0014a0007c0119t0001g0122others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.2846-3799A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933039 | ||||||
| chr19:16933135
|
G | C | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2846-3895C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933135 | ||||||
| chr19:16933251
|
GA | G | 6 | a0017c0147t0001g0009a0028c0181t0002g0060a0028c0182t0001g0062others(3): Show | 6 | HG02055.hp2 HG02647.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2846-4012delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933251 | ||||||
| chr19:16933296
|
T | C | 36 | a0002c0056t0001g0081a0002c0176t0001g0014a0004c0180t0001g0041others(33): Show | 36 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.2846-4056A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933296 | ||||||
| chr19:16933352
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2846-4112G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933352 | ||||||
| chr19:16933371
|
A | G | 22 | a0007c0119t0001g0122a0016c0050t0001g0095a0017c0147t0001g0009others(19): Show | 22 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2846-4131T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933371 | ||||||
| chr19:16933391
|
A | C | 6 | a0017c0147t0001g0009a0028c0114t0001g0100a0028c0181t0002g0060others(3): Show | 6 | HG02647.hp1 HG03195.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2846-4151T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933391 | ||||||
| chr19:16933418
|
A | G | 22 | a0007c0119t0001g0122a0016c0050t0001g0095a0017c0147t0001g0009others(19): Show | 22 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2846-4178T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933418 | ||||||
| chr19:16933535
|
G | A | 22 | a0007c0119t0001g0122a0016c0050t0001g0095a0017c0147t0001g0009others(19): Show | 22 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2846-4295C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933535 | ||||||
| chr19:16933555
|
ACATACT | A | 4 | a0028c0114t0001g0100a0028c0181t0002g0060a0028c0182t0001g0062others(1): Show | 4 | HG02647.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2846-4321_2846-431 others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933555 | ||||||
| chr19:16933710
|
G | A | 1 | a0065c0101t0001g0001 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2846-4470C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933710 | ||||||
| chr19:16933743
|
T | C | 4 | a0010c0004t0001g0201a0049c0154t0001g0195a0054c0159t0001g0128others(1): Show | 4 | HG02698.hp2 HG03927.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2846-4503A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933743 | ||||||
| chr19:16933805
|
C | T | 1 | a0064c0161t0002g0187 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2846-4565G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933805 | ||||||
| chr19:16933806
|
G | T | 2 | a0063c0144t0001g0118a0124c0186t0001g0049 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2846-4566C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933806 | ||||||
| chr19:16933953
|
T | C | 36 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.2845+4442A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16933953 | ||||||
| chr19:16934065
|
A | G | 8 | a0001c0007t0002g0246a0004c0005t0002g0042a0004c0005t0002g0146others(5): Show | 8 | HG00609.hp1 HG02040.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.2845+4330T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16934065 | ||||||
| chr19:16934115
|
G | A | 37 | a0002c0056t0001g0081a0002c0176t0001g0014a0007c0119t0001g0122others(34): Show | 37 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.2845+4280C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16934115 | ||||||
| chr19:16934217
|
G | A | 1 | a0002c0120t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2845+4178C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16934217 | ||||||
| chr19:16934537
|
A | C | 7 | a0029c0067t0001g0004a0030c0166t0002g0059a0030c0167t0001g0271others(4): Show | 7 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.2845+3858T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16934537 | ||||||
| chr19:16934763
|
C | A | 1 | a0007c0052t0002g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2845+3632G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16934763 | ||||||
| chr19:16934769
|
T | C | 5 | a0042c0175t0001g0075a0056c0072t0001g0094a0072c0081t0001g0067others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2845+3626A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16934769 | ||||||
| chr19:16934787
|
T | C | 1 | a0112c0135t0002g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2845+3608A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16934787 | ||||||
| chr19:16934832
|
T | C | 6 | a0030c0166t0002g0059a0030c0167t0001g0271a0035c0026t0001g0233others(3): Show | 6 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.2845+3563A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16934832 | ||||||
| chr19:16934918
|
T | C | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2845+3477A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16934918 | ||||||
| chr19:16934928
|
G | A | 6 | a0030c0166t0002g0059a0030c0167t0001g0271a0035c0026t0001g0233others(3): Show | 6 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.2845+3467C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16934928 | ||||||
| chr19:16935160
|
G | T | 1 | a0002c0176t0001g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2845+3235C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935160 | ||||||
| chr19:16935327
|
A | T | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2845+3068T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935327 | ||||||
| chr19:16935381
|
C | T | 42 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.2845+3014G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935381 | ||||||
| chr19:16935382
|
G | A | 2 | a0002c0176t0001g0014a0100c0068t0002g0159 | 2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2845+3013C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935382 | ||||||
| chr19:16935405
|
A | G | 1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2845+2990T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935405 | ||||||
| chr19:16935649
|
T | C | 13 | a0004c0180t0001g0041a0023c0031t0001g0025a0023c0031t0001g0026others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2845+2746A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935649 | ||||||
| chr19:16935660
|
C | T | 6 | a0004c0180t0001g0041a0042c0175t0001g0075a0056c0072t0001g0094others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2845+2735G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935660 | ||||||
| chr19:16935711
|
A | G | 38 | a0002c0056t0001g0081a0002c0176t0001g0014a0004c0180t0001g0041others(35): Show | 38 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.2845+2684T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935711 | ||||||
| chr19:16935930
|
A | AT | 32 | a0001c0013t0001g0090a0002c0017t0001g0162a0002c0018t0001g0115others(29): Show | 32 | HG01070.hp2 HG01071.hp2 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.2845+2464dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935930 | ||||||
| chr19:16935930
|
A | ATT | 8 | a0004c0005t0002g0046a0017c0147t0001g0009a0028c0114t0001g0100others(5): Show | 8 | HG02055.hp2 HG02647.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.2845+2463_2845+246 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935930 | ||||||
| chr19:16935966
|
C | T | 1 | a0116c0138t0001g0028 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2845+2429G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935966 | ||||||
| chr19:16935976
|
G | T | 15 | a0002c0056t0001g0081a0002c0176t0001g0014a0010c0004t0001g0068others(12): Show | 15 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.2845+2419C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16935976 | ||||||
| chr19:16936219
|
C | T | 14 | a0002c0056t0001g0081a0002c0176t0001g0014a0010c0004t0001g0068others(11): Show | 14 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2845+2176G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16936219 | ||||||
| chr19:16936220
|
G | A | 1 | a0015c0008t0004g0278 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2845+2175C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16936220 | ||||||
| chr19:16936222
|
C | T | 5 | a0003c0002t0002g0039a0007c0053t0001g0156a0008c0160t0001g0040others(2): Show | 5 | HG02027.hp2 HG02698.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.2845+2173G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16936222 | ||||||
| chr19:16936225
|
G | C | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2845+2170C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16936225 | ||||||
| chr19:16936313
|
T | C | 7 | a0017c0147t0001g0009a0028c0114t0001g0100a0028c0181t0002g0060others(4): Show | 7 | HG02055.hp2 HG02647.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2845+2082A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16936313 | ||||||
| chr19:16936463
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2845+1932G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16936463 | ||||||
| chr19:16936658
|
C | T | 1 | a0103c0129t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2845+1737G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16936658 | ||||||
| chr19:16936961
|
G | A | 5 | a0003c0002t0002g0039a0007c0053t0001g0156a0008c0160t0001g0040others(2): Show | 5 | HG02027.hp2 HG02698.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.2845+1434C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16936961 | ||||||
| chr19:16936963
|
T | C | 11 | a0001c0001t0002g0219a0001c0001t0002g0248a0008c0009t0001g0247others(8): Show | 11 | HG00099.hp1 HG00735.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.2845+1432A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16936963 | ||||||
| chr19:16937049
|
C | G | 1 | a0001c0001t0002g0266 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2845+1346G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937049 | ||||||
| chr19:16937063
|
G | GCCTT | 125 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.2845+1328_2845+133 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937063 | ||||||
| chr19:16937063
|
G | GCCTTCCT others(1): Show |
11 | a0002c0056t0001g0081a0017c0147t0001g0009a0030c0167t0001g0271others(8): Show | 11 | HG00735.hp2 HG01361.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2845+1324_2845+133 others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937063 | ||||||
| chr19:16937063
|
G | GCCTTCCT others(5): Show |
8 | a0016c0117t0001g0114a0028c0114t0001g0100a0028c0181t0002g0060others(5): Show | 8 | HG01168.hp1 HG01169.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2845+1320_2845+133 others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937063 | ||||||
| chr19:16937063
|
G | GCCTTCCT others(9): Show |
3 | a0002c0176t0001g0014a0042c0175t0001g0075a0100c0068t0002g0159 | 3 | HG01891.hp2 HG02257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2845+1316_2845+133 others(20): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937063 | ||||||
| chr19:16937063
|
G | GCCTTCCT others(13): Show |
1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2845+1312_2845+133 others(24): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937063 | ||||||
| chr19:16937063
|
G | GCCTTCCT others(17): Show |
4 | a0010c0004t0001g0068a0029c0067t0001g0004a0045c0118t0001g0024others(1): Show | 4 | HG02922.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2845+1308_2845+133 others(28): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937063 | ||||||
| chr19:16937065
|
C | G | 1 | a0012c0083t0001g0132 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2845+1330G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937065 | ||||||
| chr19:16937249
|
C | G | 1 | a0066c0103t0002g0022 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2845+1146G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937249 | ||||||
| chr19:16937292
|
G | A | 1 | a0016c0117t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2845+1103C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937292 | ||||||
| chr19:16937382
|
T | C | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2845+1013A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937382 | ||||||
| chr19:16937408
|
C | T | 7 | a0017c0147t0001g0009a0028c0114t0001g0100a0028c0181t0002g0060others(4): Show | 7 | HG02055.hp2 HG02647.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2845+987G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937408 | ||||||
| chr19:16937442
|
C | T | 38 | a0002c0056t0001g0081a0002c0176t0001g0014a0007c0119t0001g0122others(35): Show | 38 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.2845+953G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937442 | ||||||
| chr19:16937444
|
T | C | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2845+951A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937444 | ||||||
| chr19:16937452
|
G | A | 1 | a0002c0120t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2845+943C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937452 | ||||||
| chr19:16937521
|
G | A | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2845+874C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937521 | ||||||
| chr19:16937650
|
C | CT | 32 | a0001c0001t0002g0266a0001c0013t0001g0090a0001c0013t0001g0138others(29): Show | 32 | HG00099.hp2 HG01109.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.2845+744dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937650 | ||||||
| chr19:16937650
|
C | CTT | 9 | a0003c0002t0002g0039a0005c0003t0002g0125a0007c0053t0001g0156others(6): Show | 9 | HG00639.hp2 HG01496.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.2845+743_2845+744d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937650 | ||||||
| chr19:16937650
|
CT | C | 13 | a0001c0001t0002g0199a0005c0003t0002g0236a0005c0121t0002g0267others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2845+744delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937650 | ||||||
| chr19:16937650
|
CTT | C | 12 | a0007c0119t0001g0122a0016c0050t0001g0095a0017c0147t0001g0009others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2845+743_2845+744d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937650 | ||||||
| chr19:16937650
|
CTTTT | C | 15 | a0002c0056t0001g0081a0016c0117t0001g0114a0029c0067t0001g0004others(12): Show | 15 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.2845+741_2845+744d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937650 | ||||||
| chr19:16937673
|
G | A | 1 | a0002c0176t0001g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2845+722C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937673 | ||||||
| chr19:16937684
|
G | A | 1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2845+711C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937684 | ||||||
| chr19:16937687
|
C | A | 18 | a0007c0119t0001g0122a0016c0050t0001g0095a0017c0147t0001g0009others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.2845+708G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937687 | ||||||
| chr19:16937702
|
G | T | 3 | a0007c0119t0001g0122a0016c0050t0001g0095a0093c0177t0001g0072 | 3 | HG02559.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2845+693C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937702 | ||||||
| chr19:16937714
|
G | A | 1 | a0006c0006t0001g0086 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2845+681C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937714 | ||||||
| chr19:16937739
|
G | A | 18 | a0007c0119t0001g0122a0016c0050t0001g0095a0017c0147t0001g0009others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.2845+656C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937739 | ||||||
| chr19:16937776
|
C | A | 1 | a0002c0176t0001g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2845+619G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937776 | ||||||
| chr19:16937787
|
G | A | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2845+608C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937787 | ||||||
| chr19:16937943
|
C | T | 2 | a0045c0118t0001g0024a0113c0136t0002g0169 | 2 | HG02922.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.2845+452G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937943 | ||||||
| chr19:16937945
|
C | T | 1 | a0012c0083t0001g0132 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2845+450G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16937945 | ||||||
| chr19:16938038
|
C | T | 42 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.2845+357G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16938038 | ||||||
| chr19:16938123
|
T | TCCTGTGT others(19): Show |
1 | a0002c0176t0001g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2845+246_2845+271d others(28): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16938123 | ||||||
| chr19:16938154
|
TGTATTCA others(8): Show |
T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2845+226_2845+240d others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16938154 | ||||||
| chr19:16938167
|
T | C | 2 | a0063c0144t0001g0118a0124c0186t0001g0049 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2845+228A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16938167 | ||||||
| chr19:16938242
|
C | T | 3 | a0002c0120t0001g0074a0063c0144t0001g0118a0124c0186t0001g0049 | 3 | HG01884.hp1 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2845+153G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16938242 | ||||||
| chr19:16938290
|
T | C | 1 | a0069c0098t0001g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2845+105A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16938290 | ||||||
| chr19:16938302
|
G | A | 1 | a0002c0120t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2845+93C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 23/41 | chr19 | 16938302 | ||||||
| chr19:16938484
|
G | C | 3 | a0045c0118t0001g0024a0088c0047t0001g0161a0100c0068t0002g0159 | 3 | HG01891.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2794-38C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16938484 | ||||||
| chr19:16938515
|
C | A | 1 | a0073c0082t0001g0069 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2794-69G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16938515 | ||||||
| chr19:16938575
|
C | T | 1 | a0009c0010t0002g0257 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2794-129G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16938575 | ||||||
| chr19:16938776
|
G | A | 37 | a0001c0001t0002g0266a0001c0013t0001g0090a0001c0013t0001g0138others(34): Show | 37 | HG00099.hp2 HG01109.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.2794-330C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16938776 | ||||||
| chr19:16938957
|
C | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0185 | 2 | NA18971.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2794-511G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16938957 | ||||||
| chr19:16939022
|
T | C | 93 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.2794-576A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939022 | ||||||
| chr19:16939105
|
C | A | 1 | a0026c0127t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2794-659G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939105 | ||||||
| chr19:16939149
|
T | TTTTA | 37 | a0001c0001t0002g0276a0003c0002t0002g0039a0003c0002t0002g0196others(34): Show | 37 | HG00609.hp2 HG01081.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.2794-707_2794-704d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939149 | ||||||
| chr19:16939149
|
TTTTA | T | 31 | a0001c0007t0002g0036a0002c0017t0001g0112a0003c0002t0002g0092others(28): Show | 31 | HG00597.hp1 HG01070.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2794-707_2794-704d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939149 | ||||||
| chr19:16939149
|
TTTTATTT others(1): Show |
T | 3 | a0063c0144t0001g0118a0100c0068t0002g0159a0110c0115t0001g0098 | 3 | HG01891.hp2 HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2794-711_2794-704d others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939149 | ||||||
| chr19:16939149
|
TTTTATTT others(5): Show |
T | 4 | a0010c0004t0001g0068a0045c0118t0001g0024a0088c0047t0001g0161others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2794-715_2794-704d others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939149 | ||||||
| chr19:16939149
|
TTTTATTT others(9): Show |
T | 1 | a0016c0117t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2794-719_2794-704d others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939149 | ||||||
| chr19:16939171
|
TTATTTAT others(17): Show |
T | 9 | a0001c0001t0002g0248a0008c0009t0001g0247a0010c0004t0001g0088others(6): Show | 9 | HG00099.hp1 HG00735.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.2794-749_2794-726d others(26): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939171 | ||||||
| chr19:16939175
|
TTATTTAT others(13): Show |
T | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0277others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2794-749_2794-730d others(22): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939175 | ||||||
| chr19:16939179
|
T | C | 7 | a0023c0031t0001g0025a0023c0031t0001g0026a0023c0075t0001g0137others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.2794-733A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939179 | ||||||
| chr19:16939179
|
TTATTTAT others(9): Show |
T | 11 | a0002c0062t0002g0176a0005c0131t0002g0063a0013c0078t0002g0171others(8): Show | 11 | HG00423.hp2 HG00438.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.2794-749_2794-734d others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939179 | ||||||
| chr19:16939183
|
T | C | 9 | a0023c0031t0001g0025a0023c0031t0001g0026a0023c0075t0001g0137others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2794-737A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939183 | ||||||
| chr19:16939187
|
T | C | 43 | a0001c0007t0002g0036a0002c0017t0001g0162a0002c0019t0001g0008others(40): Show | 43 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.2794-741A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939187 | ||||||
| chr19:16939203
|
G | A | 75 | a0001c0001t0002g0266a0001c0007t0002g0036a0001c0013t0001g0090others(72): Show | 75 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.2794-757C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939203 | ||||||
| chr19:16939203
|
G | C | 94 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.2794-757C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939203 | ||||||
| chr19:16939207
|
C | A | 1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2794-761G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939207 | ||||||
| chr19:16939222
|
T | C | 174 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2794-776A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939222 | ||||||
| chr19:16939260
|
G | A | 37 | a0001c0001t0002g0266a0001c0013t0001g0138a0001c0013t0001g0261others(34): Show | 37 | HG00099.hp2 HG01109.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.2794-814C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939260 | ||||||
| chr19:16939283
|
T | C | 1 | a0120c0164t0001g0013 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2794-837A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939283 | ||||||
| chr19:16939447
|
G | A | 1 | a0003c0151t0001g0143 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2794-1001C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939447 | ||||||
| chr19:16939452
|
G | A | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2794-1006C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939452 | ||||||
| chr19:16939584
|
G | A | 2 | a0002c0120t0001g0074a0002c0176t0001g0014 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2794-1138C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939584 | ||||||
| chr19:16939588
|
G | A | 1 | a0109c0184t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2794-1142C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939588 | ||||||
| chr19:16939619
|
T | C | 1 | a0003c0002t0002g0039 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2794-1173A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939619 | ||||||
| chr19:16939758
|
T | C | 166 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.2794-1312A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939758 | ||||||
| chr19:16939879
|
G | T | 43 | a0001c0001t0002g0266a0001c0013t0001g0138a0001c0013t0001g0261others(40): Show | 43 | HG00099.hp2 HG01070.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.2794-1433C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939879 | ||||||
| chr19:16939882
|
G | C | 1 | a0001c0001t0002g0276 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2794-1436C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939882 | ||||||
| chr19:16939902
|
T | G | 164 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2794-1456A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939902 | ||||||
| chr19:16939929
|
T | C | 1 | a0069c0098t0001g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2794-1483A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939929 | ||||||
| chr19:16939953
|
C | T | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2794-1507G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16939953 | ||||||
| chr19:16940056
|
G | T | 85 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.2794-1610C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940056 | ||||||
| chr19:16940103
|
G | A | 35 | a0001c0007t0002g0036a0001c0013t0001g0090a0002c0017t0001g0162others(32): Show | 35 | HG00597.hp1 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.2794-1657C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940103 | ||||||
| chr19:16940191
|
C | T | 11 | a0007c0119t0001g0122a0023c0031t0001g0025a0023c0031t0001g0026others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2794-1745G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940191 | ||||||
| chr19:16940207
|
C | T | 1 | a0036c0025t0002g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2794-1761G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940207 | ||||||
| chr19:16940422
|
C | T | 1 | a0037c0093t0001g0274 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2794-1976G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940422 | ||||||
| chr19:16940464
|
TG | T | 168 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2794-2019delC | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940464 | ||||||
| chr19:16940599
|
C | T | 2 | a0001c0001t0002g0199a0013c0024t0002g0178 | 2 | HG01496.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2794-2153G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940599 | ||||||
| chr19:16940610
|
T | C | 2 | a0003c0151t0001g0143a0044c0021t0002g0269 | 2 | HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2794-2164A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940610 | ||||||
| chr19:16940624
|
A | C | 86 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.2794-2178T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940624 | ||||||
| chr19:16940783
|
C | T | 1 | a0026c0127t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2794-2337G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940783 | ||||||
| chr19:16940848
|
C | T | 2 | a0010c0004t0001g0068a0122c0162t0001g0019 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2794-2402G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940848 | ||||||
| chr19:16940861
|
T | A | 168 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2794-2415A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940861 | ||||||
| chr19:16940883
|
G | A | 82 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.2794-2437C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940883 | ||||||
| chr19:16940967
|
G | A | 15 | a0001c0013t0001g0090a0002c0017t0001g0162a0002c0019t0001g0008others(12): Show | 15 | HG00735.hp2 HG00741.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.2794-2521C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940967 | ||||||
| chr19:16940991
|
C | T | 171 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.2794-2545G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16940991 | ||||||
| chr19:16941121
|
C | A | 1 | a0019c0039t0001g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2794-2675G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941121 | ||||||
| chr19:16941123
|
G | C | 87 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.2794-2677C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941123 | ||||||
| chr19:16941364
|
C | T | 2 | a0029c0067t0001g0004a0120c0164t0001g0013 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2794-2918G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941364 | ||||||
| chr19:16941367
|
A | ATC | 80 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0001t0002g0248others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.2794-2923_2794-292 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941367 | ||||||
| chr19:16941380
|
C | T | 1 | a0021c0037t0002g0256 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2794-2934G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941380 | ||||||
| chr19:16941386
|
T | A | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2794-2940A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941386 | ||||||
| chr19:16941451
|
C | T | 2 | a0045c0051t0001g0083a0120c0164t0001g0013 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2794-3005G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941451 | ||||||
| chr19:16941498
|
G | C | 28 | a0001c0007t0002g0036a0001c0013t0001g0261a0001c0033t0002g0027others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.2794-3052C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941498 | ||||||
| chr19:16941587
|
G | C | 68 | a0001c0001t0002g0276a0001c0007t0002g0036a0001c0013t0001g0138others(65): Show | 68 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.2794-3141C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941587 | ||||||
| chr19:16941664
|
T | G | 1 | a0040c0074t0002g0212 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2794-3218A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941664 | ||||||
| chr19:16941845
|
T | C | 1 | a0001c0001t0002g0158 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2794-3399A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941845 | ||||||
| chr19:16941863
|
T | C | 3 | a0001c0001t0002g0248a0010c0004t0001g0254a0113c0136t0002g0169 | 3 | HG00099.hp1 HG01109.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.2794-3417A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941863 | ||||||
| chr19:16941903
|
C | T | 112 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0219others(109): Show | 112 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.2794-3457G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941903 | ||||||
| chr19:16941946
|
G | A | 1 | a0027c0035t0001g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2794-3500C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941946 | ||||||
| chr19:16941950
|
C | T | 1 | a0012c0083t0001g0132 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2794-3504G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16941950 | ||||||
| chr19:16942236
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2793+3313G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942236 | ||||||
| chr19:16942256
|
G | A | 1 | a0009c0010t0002g0257 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2793+3293C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942256 | ||||||
| chr19:16942342
|
G | A | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2793+3207C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942342 | ||||||
| chr19:16942418
|
C | T | 1 | a0045c0051t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2793+3131G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942418 | ||||||
| chr19:16942440
|
C | G | 1 | a0026c0127t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2793+3109G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942440 | ||||||
| chr19:16942440
|
C | T | 4 | a0002c0056t0001g0081a0007c0016t0001g0007a0062c0069t0001g0071others(1): Show | 4 | HG02109.hp2 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2793+3109G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942440 | ||||||
| chr19:16942487
|
C | T | 25 | a0007c0053t0001g0156a0010c0004t0001g0068a0017c0147t0001g0009others(22): Show | 25 | HG01361.hp1 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.2793+3062G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942487 | ||||||
| chr19:16942595
|
G | A | 7 | a0021c0143t0001g0012a0034c0070t0002g0091a0034c0071t0001g0070others(4): Show | 7 | HG01109.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2793+2954C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942595 | ||||||
| chr19:16942609
|
G | T | 4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2793+2940C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942609 | ||||||
| chr19:16942719
|
G | A | 1 | a0050c0148t0002g0235 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2793+2830C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942719 | ||||||
| chr19:16942864
|
C | T | 33 | a0001c0013t0001g0138a0007c0016t0001g0123a0007c0016t0001g0124others(30): Show | 33 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.2793+2685G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942864 | ||||||
| chr19:16942915
|
C | T | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2793+2634G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942915 | ||||||
| chr19:16942935
|
G | C | 77 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(74): Show | 77 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.2793+2614C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942935 | ||||||
| chr19:16942950
|
T | C | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2793+2599A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942950 | ||||||
| chr19:16942973
|
T | C | 4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2793+2576A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16942973 | ||||||
| chr19:16943008
|
T | C | 1 | a0001c0001t0002g0266 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2793+2541A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943008 | ||||||
| chr19:16943008
|
TTTC | T | 55 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(52): Show | 55 | HG00735.hp2 HG00741.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.2793+2538_2793+254 others(7): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943008 | ||||||
| chr19:16943010
|
TC | T | 12 | a0007c0053t0001g0156a0018c0038t0002g0193a0020c0011t0001g0017others(9): Show | 12 | HG01433.hp1 HG01884.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.2793+2538delG | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943010 | ||||||
| chr19:16943011
|
C | T | 46 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0033t0002g0002others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2793+2538G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943011 | ||||||
| chr19:16943031
|
A | G | 45 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(42): Show | 45 | HG00735.hp2 HG01099.hp2 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.2793+2518T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943031 | ||||||
| chr19:16943064
|
G | A | 4 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2793+2485C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943064 | ||||||
| chr19:16943167
|
C | A | 1 | a0029c0137t0002g0270 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2793+2382G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943167 | ||||||
| chr19:16943363
|
C | T | 1 | a0093c0177t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2793+2186G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943363 | ||||||
| chr19:16943383
|
C | CTTTA | 3 | a0001c0001t0002g0266a0023c0075t0001g0137a0042c0174t0001g0160 | 3 | HG02300.hp1 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2793+2162_2793+216 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943383 | ||||||
| chr19:16943402
|
T | TATTC | 4 | a0010c0004t0001g0068a0017c0147t0001g0009a0109c0184t0001g0057others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2793+2143_2793+214 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943402 | ||||||
| chr19:16943604
|
C | T | 2 | a0001c0013t0001g0138a0124c0186t0001g0049 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2793+1945G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943604 | ||||||
| chr19:16943682
|
T | C | 81 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(78): Show | 81 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.2793+1867A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943682 | ||||||
| chr19:16943700
|
T | C | 81 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(78): Show | 81 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.2793+1849A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943700 | ||||||
| chr19:16943747
|
C | T | 1 | a0038c0109t0002g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2793+1802G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943747 | ||||||
| chr19:16943753
|
T | A | 81 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(78): Show | 81 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.2793+1796A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943753 | ||||||
| chr19:16943817
|
C | T | 1 | a0033c0040t0001g0265 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2793+1732G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943817 | ||||||
| chr19:16943826
|
C | T | 58 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(55): Show | 58 | HG00735.hp2 HG01099.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.2793+1723G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16943826 | ||||||
| chr19:16944036
|
C | T | 1 | a0002c0017t0001g0113 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2793+1513G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944036 | ||||||
| chr19:16944073
|
AC | A | 4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2793+1475delG | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944073 | ||||||
| chr19:16944076
|
C | G | 4 | a0016c0117t0001g0114a0023c0031t0001g0025a0023c0031t0001g0026others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2793+1473G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944076 | ||||||
| chr19:16944123
|
C | T | 4 | a0010c0004t0001g0068a0017c0147t0001g0009a0109c0184t0001g0057others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2793+1426G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944123 | ||||||
| chr19:16944148
|
C | T | 79 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(76): Show | 79 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.2793+1401G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944148 | ||||||
| chr19:16944176
|
C | T | 1 | a0094c0060t0001g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2793+1373G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944176 | ||||||
| chr19:16944511
|
G | T | 79 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(76): Show | 79 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.2793+1038C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944511 | ||||||
| chr19:16944594
|
T | C | 79 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(76): Show | 79 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.2793+955A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944594 | ||||||
| chr19:16944720
|
TGACCTGT others(17): Show |
T | 79 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(76): Show | 79 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.2793+805_2793+828d others(26): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944720 | ||||||
| chr19:16944867
|
T | A | 79 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(76): Show | 79 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.2793+682A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944867 | ||||||
| chr19:16944870
|
C | T | 2 | a0004c0005t0002g0042a0024c0092t0001g0260 | 2 | NA18612.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2793+679G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944870 | ||||||
| chr19:16944888
|
G | GGCT | 79 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(76): Show | 79 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.2793+658_2793+660d others(5): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944888 | ||||||
| chr19:16944896
|
G | A | 28 | a0001c0001t0002g0199a0001c0001t0002g0219a0001c0001t0002g0276others(25): Show | 28 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2793+653C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944896 | ||||||
| chr19:16944909
|
T | C | 75 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(72): Show | 75 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.2793+640A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16944909 | ||||||
| chr19:16945043
|
C | T | 1 | a0090c0064t0002g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2793+506G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16945043 | ||||||
| chr19:16945140
|
C | A | 79 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(76): Show | 79 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.2793+409G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16945140 | ||||||
| chr19:16945219
|
G | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2793+330C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16945219 | ||||||
| chr19:16945231
|
G | T | 1 | a0076c0088t0001g0084 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2793+318C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16945231 | ||||||
| chr19:16945335
|
G | A | 122 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(119): Show |
intron_variant | MODIFIER | c.2793+214C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16945335 | ||||||
| chr19:16945349
|
G | A | 1 | a0029c0125t0002g0034 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2793+200C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16945349 | ||||||
| chr19:16945484
|
G | C | 79 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(76): Show | 79 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.2793+65C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 22/41 | chr19 | 16945484 | ||||||
| chr19:16945747
|
T | A | 1 | a0002c0017t0001g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663-68A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16945747 | ||||||
| chr19:16945866
|
T | C | 126 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(123): Show |
intron_variant | MODIFIER | c.2663-187A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16945866 | ||||||
| chr19:16945918
|
C | T | 5 | a0008c0009t0001g0217a0010c0004t0001g0243a0012c0083t0001g0132others(2): Show | 5 | HG01099.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2663-239G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16945918 | ||||||
| chr19:16945936
|
C | T | 114 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(111): Show | 114 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(111): Show |
intron_variant | MODIFIER | c.2663-257G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16945936 | ||||||
| chr19:16945956
|
C | T | 4 | a0010c0004t0001g0068a0017c0147t0001g0009a0109c0184t0001g0057others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2663-277G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16945956 | ||||||
| chr19:16945973
|
TTG | T | 4 | a0001c0013t0001g0090a0002c0019t0001g0008a0002c0019t0001g0139others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2663-296_2663-295d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16945973 | ||||||
| chr19:16945989
|
A | T | 258 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0001t0002g0185others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2663-310T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16945989 | ||||||
| chr19:16946085
|
G | C | 1 | a0029c0125t0002g0034 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2663-406C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946085 | ||||||
| chr19:16946169
|
T | A | 116 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(113): Show | 116 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(113): Show |
intron_variant | MODIFIER | c.2663-490A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946169 | ||||||
| chr19:16946173
|
T | TG | 117 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(114): Show | 117 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(114): Show |
intron_variant | MODIFIER | c.2663-495dupC | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946173 | ||||||
| chr19:16946177
|
T | TTG | 3 | a0001c0007t0002g0036a0002c0062t0002g0176a0006c0132t0002g0087 | 3 | HG01346.hp1 HG01934.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2663-500_2663-499d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946177 | ||||||
| chr19:16946189
|
G | A | 117 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(114): Show | 117 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(114): Show |
intron_variant | MODIFIER | c.2663-510C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946189 | ||||||
| chr19:16946294
|
T | A | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01099.hp2 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.2663-615A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946294 | ||||||
| chr19:16946335
|
ATATG | A | 4 | a0010c0004t0001g0068a0017c0147t0001g0009a0109c0184t0001g0057others(1): Show | 4 | HG02965.hp1 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2663-660_2663-657d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946335 | ||||||
| chr19:16946362
|
T | G | 4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2663-683A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946362 | ||||||
| chr19:16946392
|
T | C | 45 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0033t0002g0002others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2662+682A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946392 | ||||||
| chr19:16946436
|
A | AATGCATG others(35): Show |
1 | a0117c0110t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2662+596_2662+637d others(44): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946436 | ||||||
| chr19:16946460
|
T | C | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2662+614A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946460 | ||||||
| chr19:16946515
|
TTG | T | 125 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(122): Show |
intron_variant | MODIFIER | c.2662+557_2662+558d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946515 | ||||||
| chr19:16946552
|
C | T | 1 | a0038c0099t0002g0224 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2662+522G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946552 | ||||||
| chr19:16946648
|
A | G | 1 | a0067c0094t0002g0145 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2662+426T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946648 | ||||||
| chr19:16946649
|
T | C | 4 | a0016c0117t0001g0114a0023c0031t0001g0025a0023c0031t0001g0026others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2662+425A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946649 | ||||||
| chr19:16946688
|
G | A | 123 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(120): Show |
intron_variant | MODIFIER | c.2662+386C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946688 | ||||||
| chr19:16946741
|
G | A | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2662+333C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946741 | ||||||
| chr19:16946750
|
T | G | 53 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0013t0001g0138others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.2662+324A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946750 | ||||||
| chr19:16946784
|
C | T | 48 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0033t0002g0002others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2662+290G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946784 | ||||||
| chr19:16946885
|
G | A | 1 | a0011c0090t0001g0255 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2662+189C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 21/41 | chr19 | 16946885 | ||||||
| chr19:16947378
|
T | C | 4 | a0016c0117t0001g0114a0023c0031t0001g0025a0023c0031t0001g0026others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-151A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947378 | ||||||
| chr19:16947382
|
C | T | 1 | a0007c0170t0002g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2509-155G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947382 | ||||||
| chr19:16947459
|
C | T | 2 | a0001c0013t0001g0138a0124c0186t0001g0049 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2509-232G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947459 | ||||||
| chr19:16947552
|
A | T | 1 | a0011c0091t0001g0179 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2509-325T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947552 | ||||||
| chr19:16947631
|
C | T | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2509-404G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947631 | ||||||
| chr19:16947717
|
TC | T | 277 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.2509-491delG | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947717 | ||||||
| chr19:16947845
|
G | A | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2509-618C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947845 | ||||||
| chr19:16947864
|
T | A | 4 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2509-637A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947864 | ||||||
| chr19:16947884
|
G | T | 2 | a0003c0045t0002g0218a0018c0155t0002g0215 | 2 | NA19012.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2509-657C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947884 | ||||||
| chr19:16947931
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2509-704A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947931 | ||||||
| chr19:16947984
|
G | A | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2509-757C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16947984 | ||||||
| chr19:16948003
|
T | C | 234 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0001t0002g0185others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.2509-776A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948003 | ||||||
| chr19:16948083
|
C | T | 114 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.2509-856G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948083 | ||||||
| chr19:16948089
|
C | T | 122 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(119): Show |
intron_variant | MODIFIER | c.2509-862G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948089 | ||||||
| chr19:16948091
|
T | C | 122 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(119): Show |
intron_variant | MODIFIER | c.2509-864A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948091 | ||||||
| chr19:16948399
|
G | T | 123 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(120): Show |
intron_variant | MODIFIER | c.2509-1172C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948399 | ||||||
| chr19:16948465
|
G | A | 51 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0033t0002g0002others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.2509-1238C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948465 | ||||||
| chr19:16948592
|
A | G | 127 | a0001c0001t0002g0248a0001c0001t0002g0266a0001c0001t0002g0277others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(124): Show |
intron_variant | MODIFIER | c.2509-1365T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948592 | ||||||
| chr19:16948730
|
T | A | 1 | a0110c0115t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2509-1503A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948730 | ||||||
| chr19:16948812
|
A | G | 4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-1585T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948812 | ||||||
| chr19:16948815
|
G | A | 4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-1588C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948815 | ||||||
| chr19:16948825
|
A | G | 4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-1598T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948825 | ||||||
| chr19:16948827
|
G | A | 4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-1600C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948827 | ||||||
| chr19:16948835
|
G | A | 4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-1608C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948835 | ||||||
| chr19:16948840
|
A | AGGGAACA others(13): Show |
1 | a0110c0115t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2509-1614_2509-161 others(24): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948840 | ||||||
| chr19:16948840
|
A | AGGGAAGA others(13): Show |
3 | a0007c0016t0001g0124a0016c0117t0001g0114a0023c0031t0001g0025 | 3 | HG01070.hp2 HG01169.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2509-1633_2509-161 others(24): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948840 | ||||||
| chr19:16948840
|
A | AGGGAAGG others(3): Show |
4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-1614_2509-161 others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948840 | ||||||
| chr19:16948863
|
A | G | 61 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(58): Show | 61 | HG00735.hp2 HG01071.hp2 HG01099.hp2 others(58): Show |
intron_variant | MODIFIER | c.2509-1636T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948863 | ||||||
| chr19:16948867
|
G | A | 61 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(58): Show | 61 | HG00735.hp2 HG01071.hp2 HG01099.hp2 others(58): Show |
intron_variant | MODIFIER | c.2509-1640C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948867 | ||||||
| chr19:16948868
|
A | AAAGGG | 5 | a0001c0007t0002g0221a0001c0013t0001g0090a0011c0091t0001g0179others(2): Show | 5 | HG01891.hp1 HG02074.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.2509-1646_2509-164 others(9): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948868 | ||||||
| chr19:16948868
|
A | AAAGGGAA others(3): Show |
1 | a0010c0004t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2509-1651_2509-164 others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948868 | ||||||
| chr19:16948868
|
A | AAAGGGAA others(13): Show |
2 | a0001c0001t0002g0248a0113c0136t0002g0169 | 2 | HG00099.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.2509-1661_2509-164 others(24): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948868 | ||||||
| chr19:16948868
|
A | G | 62 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(59): Show | 62 | HG00735.hp2 HG01071.hp2 HG01099.hp2 others(59): Show |
intron_variant | MODIFIER | c.2509-1641T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948868 | ||||||
| chr19:16948868
|
AAAGGG | A | 93 | a0001c0001t0002g0158a0001c0001t0002g0185a0001c0001t0002g0199others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2509-1646_2509-164 others(9): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948868 | ||||||
| chr19:16948868
|
AAAGGGAA others(3): Show |
A | 3 | a0002c0059t0001g0044a0004c0005t0002g0188a0069c0098t0001g0065 | 3 | HG03130.hp2 NA18963.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.2509-1651_2509-164 others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948868 | ||||||
| chr19:16948868
|
AAAGGGAA others(8): Show |
A | 12 | a0001c0013t0001g0138a0007c0053t0001g0156a0020c0011t0001g0017others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2509-1656_2509-164 others(19): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948868 | ||||||
| chr19:16948868
|
AAAGGGAA others(13): Show |
A | 19 | a0003c0002t0002g0196a0004c0014t0002g0038a0006c0006t0001g0086others(16): Show | 19 | HG00741.hp2 HG01070.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.2509-1661_2509-164 others(24): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948868 | ||||||
| chr19:16948877
|
G | GGAGGGGA others(3): Show |
44 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(41): Show | 44 | HG00735.hp2 HG01099.hp2 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.2509-1651_2509-165 others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948877 | ||||||
| chr19:16948880
|
A | G | 17 | a0007c0016t0001g0123a0007c0052t0002g0119a0007c0119t0001g0122others(14): Show | 17 | HG01071.hp2 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2509-1653T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948880 | ||||||
| chr19:16948883
|
G | A | 8 | a0007c0016t0001g0123a0007c0052t0002g0119a0007c0119t0001g0122others(5): Show | 8 | HG01071.hp2 HG01167.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.2509-1656C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948883 | ||||||
| chr19:16948883
|
G | GAAGAGAA others(33): Show |
4 | a0028c0114t0001g0100a0028c0181t0002g0060a0028c0182t0001g0062others(1): Show | 4 | HG02647.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2509-1657_2509-165 others(44): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948883 | ||||||
| chr19:16948883
|
G | GAAGAGAA others(53): Show |
5 | a0055c0145t0001g0093a0065c0101t0001g0001a0085c0063t0001g0018others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2509-1657_2509-165 others(64): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948883 | ||||||
| chr19:16948888
|
G | A | 17 | a0007c0016t0001g0123a0007c0052t0002g0119a0007c0119t0001g0122others(14): Show | 17 | HG01071.hp2 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2509-1661C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948888 | ||||||
| chr19:16948888
|
G | GAGGGAAA others(3): Show |
44 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(41): Show | 44 | HG00735.hp2 HG01099.hp2 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.2509-1662_2509-166 others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16948888 | ||||||
| chr19:16949003
|
AAAAGAAA others(6): Show |
A | 4 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164others(1): Show | 4 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-1789_2509-177 others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949003 | ||||||
| chr19:16949047
|
C | T | 14 | a0003c0002t0002g0092a0005c0131t0002g0063a0008c0009t0001g0231others(11): Show | 14 | HG01071.hp1 HG01433.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.2509-1820G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949047 | ||||||
| chr19:16949051
|
A | AG | 13 | a0001c0007t0002g0036a0002c0058t0002g0149a0002c0062t0002g0176others(10): Show | 13 | HG00438.hp2 HG01934.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2509-1825dupC | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949051 | ||||||
| chr19:16949055
|
G | A | 69 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(66): Show | 69 | HG00735.hp2 HG00741.hp2 HG01099.hp2 others(66): Show |
intron_variant | MODIFIER | c.2509-1828C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949055 | ||||||
| chr19:16949062
|
G | C | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2509-1835C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949062 | ||||||
| chr19:16949147
|
A | G | 5 | a0016c0117t0001g0114a0023c0031t0001g0025a0023c0031t0001g0026others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2509-1920T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949147 | ||||||
| chr19:16949385
|
T | C | 1 | a0045c0051t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2509-2158A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949385 | ||||||
| chr19:16949456
|
G | C | 1 | a0110c0115t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2509-2229C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949456 | ||||||
| chr19:16949510
|
C | T | 4 | a0016c0117t0001g0114a0023c0031t0001g0025a0023c0031t0001g0026others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509-2283G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949510 | ||||||
| chr19:16949554
|
C | T | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2509-2327G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949554 | ||||||
| chr19:16949701
|
A | T | 3 | a0003c0045t0002g0052a0003c0045t0002g0218a0018c0155t0002g0215 | 3 | NA19012.hp2 NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2508+2268T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949701 | ||||||
| chr19:16949726
|
T | C | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2508+2243A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949726 | ||||||
| chr19:16949787
|
G | A | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2508+2182C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949787 | ||||||
| chr19:16949836
|
C | G | 1 | a0006c0006t0001g0220 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2508+2133G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16949836 | ||||||
| chr19:16950004
|
A | G | 70 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(67): Show | 70 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.2508+1965T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950004 | ||||||
| chr19:16950006
|
T | C | 4 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2508+1963A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950006 | ||||||
| chr19:16950020
|
A | G | 69 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(66): Show | 69 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.2508+1949T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950020 | ||||||
| chr19:16950175
|
G | A | 69 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(66): Show | 69 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.2508+1794C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950175 | ||||||
| chr19:16950368
|
A | G | 69 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(66): Show | 69 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.2508+1601T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950368 | ||||||
| chr19:16950414
|
C | T | 14 | a0001c0013t0001g0138a0007c0053t0001g0156a0017c0147t0001g0009others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2508+1555G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950414 | ||||||
| chr19:16950477
|
C | A | 1 | a0110c0115t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2508+1492G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950477 | ||||||
| chr19:16950648
|
C | T | 1 | a0015c0008t0001g0035 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2508+1321G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950648 | ||||||
| chr19:16950681
|
T | A | 11 | a0010c0004t0001g0068a0028c0114t0001g0100a0028c0181t0002g0060others(8): Show | 11 | HG00741.hp2 HG02572.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2508+1288A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950681 | ||||||
| chr19:16950725
|
C | A | 11 | a0010c0004t0001g0068a0028c0114t0001g0100a0028c0181t0002g0060others(8): Show | 11 | HG00741.hp2 HG02572.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2508+1244G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950725 | ||||||
| chr19:16950793
|
G | GA | 14 | a0004c0005t0002g0188a0028c0114t0001g0100a0028c0182t0001g0062others(11): Show | 14 | HG00741.hp2 HG01884.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.2508+1175dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950793 | ||||||
| chr19:16950793
|
G | GAA | 10 | a0001c0013t0001g0138a0007c0053t0001g0156a0020c0011t0001g0020others(7): Show | 10 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2508+1174_2508+117 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950793 | ||||||
| chr19:16950793
|
GA | G | 24 | a0001c0001t0002g0248a0001c0007t0002g0246a0001c0033t0002g0027others(21): Show | 24 | HG00099.hp1 HG00099.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.2508+1175delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16950793 | ||||||
| chr19:16951084
|
C | T | 3 | a0002c0059t0001g0044a0004c0014t0002g0222a0004c0014t0002g0223 | 3 | HG02083.hp1 HG02523.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2508+885G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16951084 | ||||||
| chr19:16951266
|
C | T | 86 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(83): Show | 86 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(83): Show |
intron_variant | MODIFIER | c.2508+703G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16951266 | ||||||
| chr19:16951362
|
G | A | 1 | a0008c0009t0001g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2508+607C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16951362 | ||||||
| chr19:16951505
|
A | G | 1 | a0040c0074t0002g0212 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2508+464T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16951505 | ||||||
| chr19:16951584
|
G | C | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2508+385C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16951584 | ||||||
| chr19:16951603
|
A | G | 1 | a0006c0015t0002g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2508+366T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16951603 | ||||||
| chr19:16951834
|
T | C | 84 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(81): Show | 84 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.2508+135A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16951834 | ||||||
| chr19:16951845
|
G | A | 1 | a0021c0037t0002g0190 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2508+124C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16951845 | ||||||
| chr19:16951857
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2508+112G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 20/41 | chr19 | 16951857 | ||||||
| chr19:16952460
|
C | T | 5 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2277-260G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16952460 | ||||||
| chr19:16952587
|
G | T | 1 | a0066c0103t0002g0022 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2277-387C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16952587 | ||||||
| chr19:16952685
|
C | A | 1 | a0124c0186t0001g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2277-485G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16952685 | ||||||
| chr19:16952707
|
TAAAAAAG others(3): Show |
T | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2277-517_2277-508d others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16952707 | ||||||
| chr19:16952722
|
A | G | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2277-522T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16952722 | ||||||
| chr19:16952763
|
G | A | 1 | a0053c0149t0001g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2277-563C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16952763 | ||||||
| chr19:16952910
|
T | C | 11 | a0001c0013t0001g0138a0020c0011t0001g0017a0020c0011t0001g0020others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2277-710A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16952910 | ||||||
| chr19:16953077
|
T | C | 2 | a0118c0139t0001g0108a0124c0186t0001g0049 | 2 | HG00741.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2277-877A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16953077 | ||||||
| chr19:16953239
|
T | G | 1 | a0030c0167t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2277-1039A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16953239 | ||||||
| chr19:16953339
|
C | CA | 7 | a0004c0014t0002g0222a0004c0014t0002g0223a0019c0039t0001g0227others(4): Show | 7 | HG00741.hp2 HG01978.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.2277-1140dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16953339 | ||||||
| chr19:16953339
|
CA | C | 59 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(56): Show | 59 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.2277-1140delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16953339 | ||||||
| chr19:16953355
|
A | G | 2 | a0044c0021t0002g0085a0064c0161t0002g0187 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2277-1155T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16953355 | ||||||
| chr19:16953520
|
C | T | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2277-1320G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16953520 | ||||||
| chr19:16953652
|
C | CA | 13 | a0001c0001t0002g0048a0004c0005t0002g0046a0004c0005t0002g0188others(10): Show | 13 | HG01109.hp1 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2277-1453dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16953652 | ||||||
| chr19:16953652
|
CA | C | 78 | a0001c0001t0002g0158a0001c0001t0002g0277a0001c0013t0001g0138others(75): Show | 78 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(75): Show |
intron_variant | MODIFIER | c.2277-1453delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16953652 | ||||||
| chr19:16953703
|
T | A | 2 | a0012c0029t0001g0151a0012c0029t0001g0152 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2277-1503A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16953703 | ||||||
| chr19:16954162
|
G | A | 1 | a0043c0022t0001g0232 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2277-1962C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16954162 | ||||||
| chr19:16954176
|
T | G | 1 | a0074c0080t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2277-1976A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16954176 | ||||||
| chr19:16954332
|
C | CA | 6 | a0001c0007t0002g0036a0002c0062t0002g0176a0006c0132t0002g0087others(3): Show | 6 | HG00741.hp2 HG01346.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.2277-2133dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16954332 | ||||||
| chr19:16954332
|
CA | C | 6 | a0017c0147t0001g0009a0023c0031t0001g0025a0040c0141t0002g0245others(3): Show | 6 | HG00140.hp2 HG01070.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.2277-2133delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16954332 | ||||||
| chr19:16954377
|
T | C | 52 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(49): Show | 52 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2277-2177A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16954377 | ||||||
| chr19:16955076
|
C | T | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2276+2777G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16955076 | ||||||
| chr19:16955202
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2276+2651C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16955202 | ||||||
| chr19:16955251
|
T | C | 52 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(49): Show | 52 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2276+2602A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16955251 | ||||||
| chr19:16955296
|
GAA | G | 84 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(81): Show | 84 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.2276+2555_2276+255 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16955296 | ||||||
| chr19:16955309
|
A | G | 1 | a0022c0106t0003g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2276+2544T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16955309 | ||||||
| chr19:16955389
|
G | A | 1 | a0001c0007t0002g0246 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2276+2464C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16955389 | ||||||
| chr19:16955870
|
C | A | 1 | a0112c0135t0002g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2276+1983G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16955870 | ||||||
| chr19:16956342
|
T | C | 1 | a0081c0079t0001g0080 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2276+1511A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16956342 | ||||||
| chr19:16956519
|
G | C | 2 | a0099c0054t0001g0003a0107c0122t0001g0023 | 2 | HG01361.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2276+1334C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16956519 | ||||||
| chr19:16956581
|
A | G | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2276+1272T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16956581 | ||||||
| chr19:16956585
|
G | A | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2276+1268C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16956585 | ||||||
| chr19:16956672
|
A | T | 1 | a0001c0033t0002g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2276+1181T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16956672 | ||||||
| chr19:16956792
|
C | T | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2276+1061G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16956792 | ||||||
| chr19:16956989
|
T | A | 1 | a0037c0104t0001g0150 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2276+864A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16956989 | ||||||
| chr19:16957046
|
T | C | 2 | a0025c0020t0001g0153a0027c0035t0001g0172 | 2 | HG01934.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2276+807A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16957046 | ||||||
| chr19:16957122
|
T | C | 1 | a0025c0020t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2276+731A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16957122 | ||||||
| chr19:16957241
|
G | T | 1 | a0059c0156t0002g0259 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2276+612C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16957241 | ||||||
| chr19:16957361
|
G | A | 2 | a0008c0009t0001g0231a0041c0023t0002g0258 | 2 | HG02135.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.2276+492C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16957361 | ||||||
| chr19:16957598
|
T | C | 1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2276+255A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16957598 | ||||||
| chr19:16957714
|
G | A | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2276+139C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16957714 | ||||||
| chr19:16957811
|
C | G | 78 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(75): Show | 78 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(75): Show |
intron_variant | MODIFIER | c.2276+42G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 19/41 | chr19 | 16957811 | ||||||
| chr19:16958088
|
GGTTAACA | G | 5 | a0001c0013t0001g0090a0002c0019t0001g0008a0002c0019t0001g0139others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2214-180_2214-174d others(9): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958088 | ||||||
| chr19:16958107
|
T | C | 8 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0001t0002g0185others(5): Show | 8 | HG00597.hp1 HG00609.hp2 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.2214-192A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958107 | ||||||
| chr19:16958227
|
T | C | 9 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0001t0002g0185others(6): Show | 9 | HG00597.hp1 HG00609.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.2214-312A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958227 | ||||||
| chr19:16958312
|
C | T | 2 | a0099c0054t0001g0003a0107c0122t0001g0023 | 2 | HG01361.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2214-397G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958312 | ||||||
| chr19:16958413
|
G | C | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2214-498C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958413 | ||||||
| chr19:16958500
|
T | C | 1 | a0007c0053t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2214-585A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958500 | ||||||
| chr19:16958571
|
G | A | 3 | a0010c0004t0001g0068a0109c0184t0001g0057a0122c0162t0001g0019 | 3 | HG02965.hp1 HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2214-656C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958571 | ||||||
| chr19:16958702
|
T | C | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2214-787A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958702 | ||||||
| chr19:16958804
|
C | CT | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2214-890dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958804 | ||||||
| chr19:16958965
|
A | G | 2 | a0023c0075t0001g0137a0042c0174t0001g0160 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2214-1050T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958965 | ||||||
| chr19:16958971
|
G | A | 1 | a0003c0002t0002g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2214-1056C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16958971 | ||||||
| chr19:16959176
|
CT | C | 5 | a0004c0100t0002g0054a0016c0050t0001g0095a0016c0185t0001g0058others(2): Show | 5 | HG01070.hp1 HG01070.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2214-1262delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959176 | ||||||
| chr19:16959331
|
C | T | 10 | a0010c0004t0001g0068a0028c0114t0001g0100a0028c0181t0002g0060others(7): Show | 10 | HG02572.hp2 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2214-1416G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959331 | ||||||
| chr19:16959528
|
G | C | 1 | a0002c0056t0001g0081 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2214-1613C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959528 | ||||||
| chr19:16959545
|
C | CT | 7 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2214-1631dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959545 | ||||||
| chr19:16959584
|
A | C | 5 | a0008c0160t0001g0040a0027c0035t0001g0045a0033c0040t0001g0265others(2): Show | 5 | HG00642.hp2 HG01081.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2214-1669T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959584 | ||||||
| chr19:16959640
|
G | A | 4 | a0065c0101t0001g0001a0085c0063t0001g0018a0086c0179t0001g0102others(1): Show | 4 | HG02451.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2214-1725C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959640 | ||||||
| chr19:16959701
|
C | T | 1 | a0004c0014t0002g0038 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2214-1786G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959701 | ||||||
| chr19:16959720
|
T | C | 2 | a0003c0151t0001g0143a0044c0021t0002g0269 | 2 | HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2214-1805A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959720 | ||||||
| chr19:16959869
|
C | T | 78 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(75): Show | 78 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(75): Show |
intron_variant | MODIFIER | c.2214-1954G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959869 | ||||||
| chr19:16959930
|
A | T | 49 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(46): Show | 49 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.2214-2015T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959930 | ||||||
| chr19:16959932
|
G | C | 1 | a0001c0001t0002g0185 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2214-2017C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959932 | ||||||
| chr19:16959976
|
C | T | 1 | a0040c0141t0002g0245 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2214-2061G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16959976 | ||||||
| chr19:16960211
|
C | CA | 29 | a0001c0013t0001g0138a0007c0016t0001g0123a0007c0016t0001g0124others(26): Show | 29 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.2214-2297dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960211 | ||||||
| chr19:16960211
|
C | CAA | 8 | a0028c0114t0001g0100a0028c0181t0002g0060a0028c0182t0001g0062others(5): Show | 8 | HG02572.hp2 HG02647.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2214-2298_2214-229 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960211 | ||||||
| chr19:16960353
|
C | T | 1 | a0046c0036t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2214-2438G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960353 | ||||||
| chr19:16960453
|
TAA | T | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2214-2540_2214-253 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960453 | ||||||
| chr19:16960567
|
CT | C | 50 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(47): Show | 50 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.2214-2653delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960567 | ||||||
| chr19:16960659
|
C | T | 3 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164 | 3 | HG02572.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2214-2744G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960659 | ||||||
| chr19:16960683
|
C | G | 1 | a0038c0099t0002g0224 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2214-2768G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960683 | ||||||
| chr19:16960722
|
T | G | 4 | a0065c0101t0001g0001a0085c0063t0001g0018a0086c0179t0001g0102others(1): Show | 4 | HG02451.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2214-2807A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960722 | ||||||
| chr19:16960759
|
G | A | 1 | a0044c0021t0002g0269 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2214-2844C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960759 | ||||||
| chr19:16960760
|
G | C | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2214-2845C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960760 | ||||||
| chr19:16960855
|
T | C | 78 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(75): Show | 78 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(75): Show |
intron_variant | MODIFIER | c.2214-2940A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16960855 | ||||||
| chr19:16961034
|
T | C | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2214-3119A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961034 | ||||||
| chr19:16961038
|
G | A | 3 | a0010c0004t0001g0068a0109c0184t0001g0057a0122c0162t0001g0019 | 3 | HG02965.hp1 HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2214-3123C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961038 | ||||||
| chr19:16961102
|
G | A | 78 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(75): Show | 78 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(75): Show |
intron_variant | MODIFIER | c.2214-3187C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961102 | ||||||
| chr19:16961126
|
C | G | 2 | a0099c0054t0001g0003a0107c0122t0001g0023 | 2 | HG01361.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2214-3211G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961126 | ||||||
| chr19:16961223
|
G | A | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2214-3308C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961223 | ||||||
| chr19:16961234
|
G | A | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2214-3319C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961234 | ||||||
| chr19:16961253
|
T | C | 8 | a0028c0114t0001g0100a0028c0181t0002g0060a0028c0182t0001g0062others(5): Show | 8 | HG00741.hp2 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2214-3338A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961253 | ||||||
| chr19:16961329
|
A | G | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2214-3414T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961329 | ||||||
| chr19:16961442
|
C | G | 85 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(82): Show | 85 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(82): Show |
intron_variant | MODIFIER | c.2214-3527G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961442 | ||||||
| chr19:16961457
|
G | A | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2214-3542C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961457 | ||||||
| chr19:16961526
|
C | A | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2214-3611G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961526 | ||||||
| chr19:16961579
|
T | G | 1 | a0041c0023t0002g0258 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2214-3664A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961579 | ||||||
| chr19:16961696
|
C | T | 3 | a0003c0045t0002g0052a0003c0045t0002g0218a0018c0155t0002g0215 | 3 | NA19012.hp2 NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2214-3781G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961696 | ||||||
| chr19:16961769
|
C | T | 1 | a0006c0006t0001g0205 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2214-3854G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961769 | ||||||
| chr19:16961770
|
G | A | 1 | a0111c0124t0002g0050 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2214-3855C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961770 | ||||||
| chr19:16961790
|
G | A | 1 | a0045c0051t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2214-3875C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961790 | ||||||
| chr19:16961933
|
C | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2214-4018G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16961933 | ||||||
| chr19:16962343
|
T | C | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2214-4428A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16962343 | ||||||
| chr19:16962391
|
G | A | 1 | a0007c0053t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2214-4476C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16962391 | ||||||
| chr19:16962576
|
T | C | 1 | a0002c0017t0001g0113 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2214-4661A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16962576 | ||||||
| chr19:16962736
|
A | G | 2 | a0012c0029t0001g0151a0012c0029t0001g0152 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2214-4821T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16962736 | ||||||
| chr19:16962788
|
G | A | 5 | a0045c0118t0001g0024a0065c0101t0001g0001a0085c0063t0001g0018others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2214-4873C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16962788 | ||||||
| chr19:16962813
|
AG | A | 46 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(43): Show | 46 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.2214-4899delC | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16962813 | ||||||
| chr19:16962889
|
A | G | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2214-4974T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16962889 | ||||||
| chr19:16963251
|
T | C | 10 | a0001c0013t0001g0138a0020c0011t0001g0017a0020c0011t0001g0020others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2214-5336A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16963251 | ||||||
| chr19:16963312
|
G | C | 1 | a0040c0141t0002g0245 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2214-5397C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16963312 | ||||||
| chr19:16963377
|
G | T | 1 | a0069c0098t0001g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2214-5462C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16963377 | ||||||
| chr19:16963497
|
C | G | 1 | a0007c0016t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2214-5582G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16963497 | ||||||
| chr19:16963583
|
C | T | 1 | a0060c0157t0002g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2214-5668G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16963583 | ||||||
| chr19:16963692
|
C | T | 1 | a0112c0135t0002g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2214-5777G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16963692 | ||||||
| chr19:16963769
|
C | T | 1 | a0061c0142t0002g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2214-5854G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16963769 | ||||||
| chr19:16963809
|
C | T | 13 | a0001c0001t0002g0147a0004c0005t0002g0188a0004c0005t0002g0211others(10): Show | 13 | HG02015.hp2 HG03669.hp1 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.2214-5894G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16963809 | ||||||
| chr19:16964087
|
G | A | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2214-6172C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16964087 | ||||||
| chr19:16964130
|
C | G | 1 | a0028c0114t0001g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2214-6215G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16964130 | ||||||
| chr19:16964183
|
T | C | 1 | a0069c0098t0001g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2214-6268A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16964183 | ||||||
| chr19:16964334
|
G | A | 2 | a0012c0029t0001g0151a0012c0029t0001g0152 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2214-6419C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16964334 | ||||||
| chr19:16964553
|
C | T | 13 | a0010c0004t0001g0068a0017c0147t0001g0009a0028c0114t0001g0100others(10): Show | 13 | HG00741.hp2 HG01884.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.2213+6338G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16964553 | ||||||
| chr19:16964693
|
C | A | 5 | a0045c0118t0001g0024a0065c0101t0001g0001a0085c0063t0001g0018others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213+6198G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16964693 | ||||||
| chr19:16964858
|
T | G | 1 | a0016c0117t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2213+6033A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16964858 | ||||||
| chr19:16964888
|
G | A | 6 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2213+6003C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16964888 | ||||||
| chr19:16964989
|
G | A | 1 | a0073c0082t0001g0069 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2213+5902C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16964989 | ||||||
| chr19:16965046
|
G | A | 1 | a0010c0004t0001g0201 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2213+5845C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16965046 | ||||||
| chr19:16965078
|
G | A | 47 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(44): Show | 47 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.2213+5813C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16965078 | ||||||
| chr19:16965129
|
G | A | 1 | a0019c0039t0001g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2213+5762C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16965129 | ||||||
| chr19:16965259
|
C | CA | 11 | a0010c0004t0001g0068a0028c0114t0001g0100a0028c0181t0002g0060others(8): Show | 11 | HG00741.hp2 HG02572.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2213+5631dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16965259 | ||||||
| chr19:16965396
|
A | G | 201 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0001t0002g0185others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.2213+5495T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16965396 | ||||||
| chr19:16965619
|
C | A | 76 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(73): Show | 76 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(73): Show |
intron_variant | MODIFIER | c.2213+5272G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16965619 | ||||||
| chr19:16965877
|
C | T | 1 | a0009c0042t0001g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2213+5014G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16965877 | ||||||
| chr19:16966046
|
C | T | 1 | a0057c0073t0001g0066 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2213+4845G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966046 | ||||||
| chr19:16966060
|
C | T | 7 | a0034c0070t0002g0091a0034c0071t0001g0070a0081c0079t0001g0080others(4): Show | 7 | HG01109.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2213+4831G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966060 | ||||||
| chr19:16966092
|
T | C | 1 | a0041c0023t0002g0258 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2213+4799A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966092 | ||||||
| chr19:16966192
|
T | C | 1 | a0021c0143t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2213+4699A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966192 | ||||||
| chr19:16966203
|
C | G | 1 | a0072c0081t0001g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2213+4688G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966203 | ||||||
| chr19:16966204
|
T | G | 2 | a0009c0010t0002g0208a0009c0010t0002g0209 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2213+4687A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966204 | ||||||
| chr19:16966209
|
T | C | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2213+4682A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966209 | ||||||
| chr19:16966218
|
C | T | 24 | a0001c0013t0001g0138a0010c0004t0001g0068a0017c0147t0001g0009others(21): Show | 24 | HG00741.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.2213+4673G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966218 | ||||||
| chr19:16966266
|
T | A | 1 | a0008c0160t0001g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2213+4625A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966266 | ||||||
| chr19:16966444
|
C | T | 2 | a0022c0032t0001g0228a0022c0032t0001g0229 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2213+4447G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966444 | ||||||
| chr19:16966604
|
G | A | 5 | a0003c0151t0001g0143a0030c0166t0002g0059a0030c0167t0001g0271others(2): Show | 5 | HG01175.hp1 HG01346.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213+4287C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966604 | ||||||
| chr19:16966842
|
A | G | 49 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(46): Show | 49 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.2213+4049T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16966842 | ||||||
| chr19:16967172
|
C | T | 1 | a0024c0092t0001g0260 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2213+3719G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967172 | ||||||
| chr19:16967313
|
G | T | 1 | a0004c0005t0002g0211 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2213+3578C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967313 | ||||||
| chr19:16967337
|
C | T | 13 | a0010c0004t0001g0068a0017c0147t0001g0009a0028c0114t0001g0100others(10): Show | 13 | HG00741.hp2 HG01884.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.2213+3554G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967337 | ||||||
| chr19:16967568
|
A | C | 5 | a0045c0118t0001g0024a0065c0101t0001g0001a0085c0063t0001g0018others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213+3323T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967568 | ||||||
| chr19:16967578
|
T | A | 277 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.2213+3313A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967578 | ||||||
| chr19:16967596
|
G | C | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2213+3295C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967596 | ||||||
| chr19:16967731
|
A | C | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2213+3160T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967731 | ||||||
| chr19:16967766
|
G | A | 1 | a0013c0049t0002g0170 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2213+3125C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967766 | ||||||
| chr19:16967811
|
C | CA | 48 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(45): Show | 48 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.2213+3079dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967811 | ||||||
| chr19:16967816
|
T | A | 168 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0001t0002g0185others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.2213+3075A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967816 | ||||||
| chr19:16967818
|
T | A | 6 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2213+3073A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967818 | ||||||
| chr19:16967863
|
T | TTGTATAT others(23): Show |
91 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0001t0002g0185others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.2213+3027_2213+302 others(34): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967863
|
T | TTGTATAT others(57): Show |
1 | a0041c0023t0002g0258 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2213+3027_2213+302 others(68): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967863
|
T | TTGTATAT others(57): Show |
47 | a0001c0001t0002g0147a0002c0018t0001g0099a0003c0002t0002g0092others(44): Show | 47 | HG00438.hp2 HG00597.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.2213+3027_2213+302 others(68): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967863
|
T | TTGTATAT others(91): Show |
1 | a0053c0149t0001g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2213+3027_2213+302 others(102): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967863
|
T | TTGTATAT others(159): Show |
1 | a0089c0065t0002g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2213+3027_2213+302 others(170): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967863
|
T | TTGTATAT others(53): Show |
4 | a0004c0005t0002g0046a0012c0028t0002g0073a0025c0020t0001g0153others(1): Show | 4 | HG01934.hp1 HG02486.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.2213+3027_2213+302 others(64): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967863
|
T | TTGTATAT others(117): Show |
1 | a0009c0042t0001g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2213+3027_2213+302 others(128): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967863
|
T | TTGTATAT others(87): Show |
3 | a0023c0031t0001g0025a0023c0031t0001g0026a0024c0030t0001g0148 | 3 | HG01070.hp2 HG01071.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2213+3027_2213+302 others(98): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967863
|
T | TTGTATAT others(117): Show |
4 | a0026c0127t0001g0240a0067c0094t0002g0145a0068c0095t0002g0064others(1): Show | 4 | HG03927.hp2 NA18944.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.2213+3027_2213+302 others(128): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967863
|
T | TTGTATAT others(117): Show |
1 | a0003c0002t0002g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2213+3027_2213+302 others(128): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967863
|
TTGTATAT others(27): Show |
T | 6 | a0002c0018t0001g0115a0002c0018t0001g0116a0016c0185t0001g0058others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2213+2994_2213+302 others(38): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967863 | ||||||
| chr19:16967874
|
T | TGCATATA others(57): Show |
2 | a0032c0043t0001g0191a0033c0040t0001g0265 | 2 | HG00642.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2213+3016_2213+301 others(68): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967874 | ||||||
| chr19:16967874
|
T | TGCATATA others(91): Show |
1 | a0006c0015t0002g0263 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2213+3016_2213+301 others(102): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967874 | ||||||
| chr19:16967884
|
C | CACACACG others(21): Show |
32 | a0001c0001t0002g0199a0001c0001t0002g0219a0001c0001t0002g0248others(29): Show | 32 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2213+3006_2213+300 others(32): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967884 | ||||||
| chr19:16967884
|
C | CACACACG others(53): Show |
1 | a0044c0021t0002g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2213+3006_2213+300 others(64): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967884 | ||||||
| chr19:16967891
|
A | G | 6 | a0041c0023t0002g0157a0045c0118t0001g0024a0065c0101t0001g0001others(3): Show | 6 | HG02451.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2213+3000T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967891 | ||||||
| chr19:16967892
|
T | C | 62 | a0001c0001t0002g0199a0001c0001t0002g0219a0001c0001t0002g0248others(59): Show | 62 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.2213+2999A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967892 | ||||||
| chr19:16967893
|
G | GTGTGTAT others(23): Show |
2 | a0026c0034t0002g0032a0026c0034t0002g0033 | 2 | NA19065.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.2213+2997_2213+299 others(34): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967893 | ||||||
| chr19:16967893
|
G | GTGTGTAT others(23): Show |
38 | a0001c0001t0002g0277a0002c0017t0001g0112a0003c0002t0002g0196others(35): Show | 38 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.2213+2997_2213+299 others(34): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967893 | ||||||
| chr19:16967893
|
G | GTGTGTAT others(55): Show |
1 | a0118c0139t0001g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2213+2997_2213+299 others(66): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967893 | ||||||
| chr19:16967893
|
G | GTGTGTAT others(117): Show |
1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2213+2997_2213+299 others(128): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967893 | ||||||
| chr19:16967893
|
G | GTGTGTAT others(119): Show |
1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2213+2997_2213+299 others(130): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967893 | ||||||
| chr19:16967893
|
G | GTGTGTAT others(55): Show |
4 | a0004c0180t0001g0041a0010c0004t0001g0243a0078c0086t0001g0242others(1): Show | 4 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2213+2997_2213+299 others(66): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967893 | ||||||
| chr19:16967893
|
G | GTGTGTGT others(25): Show |
4 | a0003c0002t0002g0186a0005c0003t0002g0051a0036c0025t0002g0189others(1): Show | 4 | HG02155.hp1 NA18959.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.2213+2966_2213+299 others(36): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967893 | ||||||
| chr19:16967893
|
G | GTGTGTGT others(89): Show |
1 | a0076c0088t0001g0084 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2213+2997_2213+299 others(100): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967893 | ||||||
| chr19:16967894
|
T | C | 2 | a0017c0147t0001g0009a0100c0068t0002g0159 | 2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2213+2997A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967894 | ||||||
| chr19:16967894
|
T | TGTGTATA others(55): Show |
1 | a0114c0113t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2213+2996_2213+299 others(66): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967894 | ||||||
| chr19:16967894
|
T | TGTGTATA others(87): Show |
8 | a0020c0011t0001g0017a0020c0011t0001g0020a0020c0011t0001g0021others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2213+2996_2213+299 others(98): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967894 | ||||||
| chr19:16967894
|
T | TGTGTATA others(119): Show |
1 | a0001c0013t0001g0138 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2213+2996_2213+299 others(130): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967894 | ||||||
| chr19:16967894
|
T | TGTGTATA others(149): Show |
3 | a0028c0114t0001g0100a0028c0182t0001g0062a0101c0126t0001g0061 | 3 | HG02647.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2213+2996_2213+299 others(160): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967894 | ||||||
| chr19:16967894
|
T | TGTGTATA others(85): Show |
5 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2213+2996_2213+299 others(96): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967894 | ||||||
| chr19:16967894
|
T | TGTGTATA others(181): Show |
1 | a0028c0181t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2213+2996_2213+299 others(192): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967894 | ||||||
| chr19:16967894
|
T | TGTGTATA others(83): Show |
1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2213+2996_2213+299 others(94): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967894 | ||||||
| chr19:16967894
|
T | TGTGTATA others(109): Show |
1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2213+2996_2213+299 others(120): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967894 | ||||||
| chr19:16967894
|
T | TGTGTATA others(79): Show |
4 | a0065c0101t0001g0001a0085c0063t0001g0018a0086c0179t0001g0102others(1): Show | 4 | HG02451.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2213+2996_2213+299 others(90): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967894 | ||||||
| chr19:16967901
|
A | G | 5 | a0045c0118t0001g0024a0065c0101t0001g0001a0085c0063t0001g0018others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213+2990T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967901 | ||||||
| chr19:16967908
|
T | C | 2 | a0011c0012t0002g0202a0033c0040t0001g0043 | 2 | NA18966.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2213+2983A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967908 | ||||||
| chr19:16967916
|
TAC | T | 3 | a0074c0080t0001g0082a0088c0047t0001g0161a0092c0173t0001g0164 | 3 | HG02572.hp2 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2213+2973_2213+297 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967916 | ||||||
| chr19:16967925
|
A | G | 18 | a0001c0033t0002g0027a0003c0002t0002g0196a0005c0003t0002g0166others(15): Show | 18 | HG00099.hp2 HG01081.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.2213+2966T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967925 | ||||||
| chr19:16967987
|
A | T | 1 | a0069c0098t0001g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2213+2904T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16967987 | ||||||
| chr19:16968053
|
A | G | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2213+2838T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16968053 | ||||||
| chr19:16968076
|
G | C | 11 | a0001c0013t0001g0138a0020c0011t0001g0017a0020c0011t0001g0020others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2213+2815C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16968076 | ||||||
| chr19:16968264
|
C | T | 8 | a0001c0001t0002g0248a0001c0013t0001g0261a0003c0002t0002g0252others(5): Show | 8 | HG00099.hp1 HG00423.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.2213+2627G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16968264 | ||||||
| chr19:16968343
|
G | A | 1 | a0025c0169t0001g0120 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2213+2548C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16968343 | ||||||
| chr19:16968455
|
C | T | 10 | a0001c0013t0001g0138a0020c0011t0001g0017a0020c0011t0001g0020others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2213+2436G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16968455 | ||||||
| chr19:16968471
|
T | C | 2 | a0099c0054t0001g0003a0107c0122t0001g0023 | 2 | HG01361.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2213+2420A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16968471 | ||||||
| chr19:16968625
|
T | TTTTA | 8 | a0028c0114t0001g0100a0028c0181t0002g0060a0028c0182t0001g0062others(5): Show | 8 | HG00741.hp2 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2213+2262_2213+226 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16968625 | ||||||
| chr19:16968726
|
C | A | 13 | a0003c0002t0002g0092a0004c0005t0002g0042a0005c0131t0002g0063others(10): Show | 13 | HG01071.hp1 HG01433.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.2213+2165G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16968726 | ||||||
| chr19:16968800
|
T | C | 10 | a0017c0147t0001g0009a0028c0114t0001g0100a0028c0181t0002g0060others(7): Show | 10 | HG00741.hp2 HG01884.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2213+2091A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16968800 | ||||||
| chr19:16968931
|
C | T | 5 | a0045c0118t0001g0024a0065c0101t0001g0001a0085c0063t0001g0018others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213+1960G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16968931 | ||||||
| chr19:16969090
|
C | T | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2213+1801G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969090 | ||||||
| chr19:16969104
|
G | C | 1 | a0105c0128t0002g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2213+1787C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969104 | ||||||
| chr19:16969241
|
G | A | 1 | a0004c0005t0002g0211 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2213+1650C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969241 | ||||||
| chr19:16969576
|
G | C | 1 | a0118c0139t0001g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2213+1315C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969576 | ||||||
| chr19:16969580
|
CT | C | 27 | a0001c0001t0002g0199a0001c0001t0002g0219a0001c0001t0002g0248others(24): Show | 27 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.2213+1310delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969580 | ||||||
| chr19:16969603
|
G | T | 1 | a0025c0020t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2213+1288C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969603 | ||||||
| chr19:16969622
|
G | A | 2 | a0028c0114t0001g0100a0101c0126t0001g0061 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2213+1269C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969622 | ||||||
| chr19:16969631
|
G | A | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2213+1260C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969631 | ||||||
| chr19:16969830
|
T | C | 77 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(74): Show | 77 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(74): Show |
intron_variant | MODIFIER | c.2213+1061A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969830 | ||||||
| chr19:16969873
|
C | CA | 16 | a0004c0005t0002g0046a0004c0005t0002g0188a0005c0003t0002g0236others(13): Show | 16 | HG01934.hp1 HG02148.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.2213+1017dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969873 | ||||||
| chr19:16969873
|
C | CAA | 62 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(59): Show | 62 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(59): Show |
intron_variant | MODIFIER | c.2213+1016_2213+101 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969873 | ||||||
| chr19:16969890
|
C | A | 34 | a0001c0001t0002g0277a0001c0013t0001g0138a0005c0003t0002g0166others(31): Show | 34 | HG00741.hp2 HG01168.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.2213+1001G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969890 | ||||||
| chr19:16969897
|
A | G | 8 | a0028c0114t0001g0100a0028c0181t0002g0060a0028c0182t0001g0062others(5): Show | 8 | HG00741.hp2 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2213+994T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969897 | ||||||
| chr19:16969901
|
A | G | 5 | a0045c0118t0001g0024a0065c0101t0001g0001a0085c0063t0001g0018others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213+990T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969901 | ||||||
| chr19:16969943
|
C | T | 2 | a0099c0054t0001g0003a0107c0122t0001g0023 | 2 | HG01361.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2213+948G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969943 | ||||||
| chr19:16969960
|
C | T | 58 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(55): Show | 58 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(55): Show |
intron_variant | MODIFIER | c.2213+931G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969960 | ||||||
| chr19:16969972
|
T | C | 2 | a0022c0032t0001g0228a0022c0032t0001g0229 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2213+919A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16969972 | ||||||
| chr19:16970010
|
G | A | 2 | a0065c0101t0001g0001a0085c0063t0001g0018 | 2 | HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2213+881C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970010 | ||||||
| chr19:16970011
|
A | G | 5 | a0029c0067t0001g0004a0074c0080t0001g0082a0088c0047t0001g0161others(2): Show | 5 | HG00741.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213+880T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970011 | ||||||
| chr19:16970017
|
A | G | 5 | a0045c0118t0001g0024a0065c0101t0001g0001a0085c0063t0001g0018others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213+874T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970017 | ||||||
| chr19:16970051
|
A | G | 1 | a0036c0025t0002g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2213+840T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970051 | ||||||
| chr19:16970078
|
CA | C | 6 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2213+812delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970078 | ||||||
| chr19:16970107
|
C | T | 7 | a0004c0005t0002g0146a0034c0070t0002g0091a0034c0071t0001g0070others(4): Show | 7 | HG01109.hp1 HG02040.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2213+784G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970107 | ||||||
| chr19:16970108
|
G | A | 1 | a0103c0129t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2213+783C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970108 | ||||||
| chr19:16970238
|
C | CA | 31 | a0001c0013t0001g0138a0002c0017t0001g0112a0007c0016t0001g0123others(28): Show | 31 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.2213+652dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970238 | ||||||
| chr19:16970238
|
C | CAA | 49 | a0001c0001t0002g0277a0002c0018t0001g0115a0002c0018t0001g0116others(46): Show | 49 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.2213+651_2213+652d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970238 | ||||||
| chr19:16970238
|
CA | C | 130 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0001t0002g0185others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.2213+652delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970238 | ||||||
| chr19:16970425
|
A | G | 13 | a0001c0001t0002g0147a0004c0005t0002g0188a0004c0005t0002g0211others(10): Show | 13 | HG02015.hp2 HG03669.hp1 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.2213+466T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970425 | ||||||
| chr19:16970553
|
T | C | 1 | a0010c0004t0001g0088 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2213+338A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970553 | ||||||
| chr19:16970632
|
C | T | 1 | a0069c0098t0001g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2213+259G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970632 | ||||||
| chr19:16970635
|
C | A | 5 | a0045c0118t0001g0024a0065c0101t0001g0001a0085c0063t0001g0018others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213+256G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970635 | ||||||
| chr19:16970640
|
A | G | 1 | a0001c0001t0002g0147 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2213+251T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970640 | ||||||
| chr19:16970842
|
G | A | 2 | a0017c0147t0001g0009a0029c0067t0001g0004 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2213+49C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 18/41 | chr19 | 16970842 | ||||||
| chr19:16971045
|
A | G | 1 | a0029c0125t0002g0034 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2071-12T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16971045 | ||||||
| chr19:16971165
|
T | C | 1 | a0001c0007t0002g0221 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2071-132A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16971165 | ||||||
| chr19:16971582
|
G | T | 6 | a0002c0017t0001g0112a0002c0018t0001g0115a0002c0018t0001g0116others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2071-549C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16971582 | ||||||
| chr19:16971589
|
G | A | 6 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2071-556C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16971589 | ||||||
| chr19:16971650
|
G | T | 38 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(35): Show | 38 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.2071-617C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16971650 | ||||||
| chr19:16971723
|
A | G | 5 | a0045c0118t0001g0024a0065c0101t0001g0001a0085c0063t0001g0018others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2071-690T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16971723 | ||||||
| chr19:16971855
|
T | G | 2 | a0001c0001t0002g0266a0113c0136t0002g0169 | 2 | HG02300.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.2071-822A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16971855 | ||||||
| chr19:16972112
|
C | T | 2 | a0001c0001t0002g0266a0113c0136t0002g0169 | 2 | HG02300.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.2071-1079G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972112 | ||||||
| chr19:16972151
|
C | T | 69 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(66): Show | 69 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(66): Show |
intron_variant | MODIFIER | c.2071-1118G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972151 | ||||||
| chr19:16972197
|
T | C | 1 | a0010c0004t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2071-1164A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972197 | ||||||
| chr19:16972240
|
T | TG | 12 | a0001c0013t0001g0138a0020c0011t0001g0017a0020c0011t0001g0020others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2071-1208dupC | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972240 | ||||||
| chr19:16972467
|
C | G | 11 | a0020c0011t0001g0017a0020c0011t0001g0020a0020c0011t0001g0021others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2071-1434G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972467 | ||||||
| chr19:16972495
|
C | T | 1 | a0006c0015t0002g0110 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2071-1462G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972495 | ||||||
| chr19:16972625
|
G | A | 73 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0017t0001g0162others(70): Show | 73 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.2071-1592C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972625 | ||||||
| chr19:16972681
|
G | A | 51 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0018t0001g0115others(48): Show | 51 | HG01081.hp1 HG01099.hp2 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.2071-1648C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972681 | ||||||
| chr19:16972724
|
G | A | 2 | a0109c0184t0001g0057a0122c0162t0001g0019 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2071-1691C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972724 | ||||||
| chr19:16972901
|
G | T | 73 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0017t0001g0162others(70): Show | 73 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.2071-1868C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972901 | ||||||
| chr19:16972940
|
G | A | 2 | a0109c0184t0001g0057a0122c0162t0001g0019 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2071-1907C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16972940 | ||||||
| chr19:16973004
|
A | G | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2071-1971T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973004 | ||||||
| chr19:16973106
|
C | G | 1 | a0010c0004t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2070+1991G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973106 | ||||||
| chr19:16973169
|
A | C | 1 | a0021c0143t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2070+1928T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973169 | ||||||
| chr19:16973388
|
G | A | 4 | a0002c0056t0001g0081a0002c0120t0001g0074a0007c0016t0001g0007others(1): Show | 4 | HG02109.hp2 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2070+1709C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973388 | ||||||
| chr19:16973435
|
C | T | 1 | a0010c0004t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2070+1662G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973435 | ||||||
| chr19:16973779
|
T | C | 84 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(81): Show | 84 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(81): Show |
intron_variant | MODIFIER | c.2070+1318A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973779 | ||||||
| chr19:16973812
|
C | T | 5 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2070+1285G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973812 | ||||||
| chr19:16973823
|
A | G | 5 | a0002c0059t0001g0044a0004c0014t0002g0222a0004c0014t0002g0223others(2): Show | 5 | HG02083.hp1 HG02155.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.2070+1274T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973823 | ||||||
| chr19:16973827
|
C | CT | 6 | a0001c0033t0002g0002a0003c0002t0002g0252a0007c0052t0002g0119others(3): Show | 6 | HG00423.hp1 HG00642.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.2070+1269dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973827 | ||||||
| chr19:16973827
|
CT | C | 5 | a0002c0058t0002g0149a0016c0050t0001g0095a0046c0036t0001g0031others(2): Show | 5 | HG01891.hp2 HG02559.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2070+1269delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973827 | ||||||
| chr19:16973827
|
CTT | C | 17 | a0001c0013t0001g0138a0003c0002t0002g0196a0014c0105t0001g0140others(14): Show | 17 | HG00741.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2070+1268_2070+126 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973827 | ||||||
| chr19:16973827
|
CTTT | C | 62 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0017t0001g0162others(59): Show | 62 | HG01081.hp1 HG01099.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.2070+1267_2070+126 others(7): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973827 | ||||||
| chr19:16973861
|
G | C | 90 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(87): Show | 90 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(87): Show |
intron_variant | MODIFIER | c.2070+1236C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973861 | ||||||
| chr19:16973987
|
G | A | 12 | a0001c0013t0001g0138a0020c0011t0001g0017a0020c0011t0001g0020others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2070+1110C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16973987 | ||||||
| chr19:16974029
|
C | A | 4 | a0065c0101t0001g0001a0085c0063t0001g0018a0086c0179t0001g0102others(1): Show | 4 | HG02451.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2070+1068G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974029 | ||||||
| chr19:16974049
|
C | T | 2 | a0017c0147t0001g0009a0029c0067t0001g0004 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2070+1048G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974049 | ||||||
| chr19:16974122
|
T | C | 87 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(84): Show | 87 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(84): Show |
intron_variant | MODIFIER | c.2070+975A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974122 | ||||||
| chr19:16974155
|
G | A | 2 | a0022c0032t0001g0228a0022c0032t0001g0229 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2070+942C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974155 | ||||||
| chr19:16974162
|
C | T | 2 | a0019c0039t0001g0227a0027c0066t0001g0016 | 2 | HG01978.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2070+935G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974162 | ||||||
| chr19:16974226
|
G | A | 84 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(81): Show | 84 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(81): Show |
intron_variant | MODIFIER | c.2070+871C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974226 | ||||||
| chr19:16974256
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2070+841G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974256 | ||||||
| chr19:16974257
|
G | A | 1 | a0054c0159t0001g0128 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2070+840C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974257 | ||||||
| chr19:16974282
|
C | A | 85 | a0001c0001t0002g0277a0001c0013t0001g0138a0002c0017t0001g0112others(82): Show | 85 | HG00741.hp2 HG01081.hp1 HG01099.hp2 others(82): Show |
intron_variant | MODIFIER | c.2070+815G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974282 | ||||||
| chr19:16974365
|
C | A | 1 | a0005c0003t0002g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2070+732G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974365 | ||||||
| chr19:16974531
|
C | T | 66 | a0001c0001t0002g0277a0002c0017t0001g0112a0002c0017t0001g0162others(63): Show | 66 | HG00741.hp2 HG01081.hp1 HG01167.hp1 others(63): Show |
intron_variant | MODIFIER | c.2070+566G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974531 | ||||||
| chr19:16974547
|
C | T | 2 | a0002c0120t0001g0074a0007c0016t0001g0007 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2070+550G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974547 | ||||||
| chr19:16974656
|
G | A | 1 | a0105c0128t0002g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2070+441C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974656 | ||||||
| chr19:16974757
|
A | G | 1 | a0067c0094t0002g0145 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2070+340T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16974757 | ||||||
| chr19:16975042
|
C | A | 1 | a0076c0088t0001g0084 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2070+55G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16975042 | ||||||
| chr19:16975055
|
A | C | 94 | a0001c0001t0002g0147a0001c0001t0002g0277a0001c0013t0001g0138others(91): Show | 94 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(91): Show |
intron_variant | MODIFIER | c.2070+42T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16975055 | ||||||
| chr19:16975086
|
C | T | 6 | a0007c0016t0001g0123a0007c0016t0001g0124a0007c0052t0002g0119others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2070+11G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 17/41 | chr19 | 16975086 | ||||||
| chr19:16975361
|
G | A | 4 | a0005c0003t0002g0244a0008c0150t0001g0273a0025c0020t0001g0104others(1): Show | 4 | HG01168.hp2 HG02683.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909-103C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 16/41 | chr19 | 16975361 | ||||||
| chr19:16975443
|
A | G | 4 | a0008c0150t0001g0273a0009c0042t0001g0194a0025c0020t0001g0104others(1): Show | 4 | HG01168.hp2 HG02683.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909-185T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 16/41 | chr19 | 16975443 | ||||||
| chr19:16975452
|
A | G | 2 | a0045c0051t0001g0083a0074c0080t0001g0082 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1909-194T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 16/41 | chr19 | 16975452 | ||||||
| chr19:16975478
|
A | T | 26 | a0007c0016t0001g0007a0007c0016t0001g0123a0007c0016t0001g0124others(23): Show | 26 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1909-220T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 16/41 | chr19 | 16975478 | ||||||
| chr19:16975536
|
G | A | 12 | a0002c0176t0001g0014a0003c0151t0001g0143a0030c0166t0002g0059others(9): Show | 12 | HG01109.hp1 HG01175.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.1909-278C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 16/41 | chr19 | 16975536 | ||||||
| chr19:16975686
|
C | A | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1908+316G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 16/41 | chr19 | 16975686 | ||||||
| chr19:16975963
|
C | T | 16 | a0001c0013t0001g0090a0001c0013t0001g0138a0007c0016t0001g0007others(13): Show | 16 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1908+39G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 16/41 | chr19 | 16975963 | ||||||
| chr19:16975987
|
G | A | 1 | a0012c0028t0002g0073 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1908+15C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 16/41 | chr19 | 16975987 | ||||||
| chr19:16976227
|
A | G | 3 | a0011c0091t0001g0179a0040c0074t0002g0212a0041c0023t0002g0258 | 3 | HG02074.hp2 NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1759-76T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976227 | ||||||
| chr19:16976246
|
C | T | 5 | a0016c0116t0001g0010a0016c0117t0001g0114a0028c0114t0001g0100others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1759-95G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976246 | ||||||
| chr19:16976247
|
G | A | 1 | a0012c0083t0001g0132 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1759-96C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976247 | ||||||
| chr19:16976274
|
GAGACCAG others(559): Show |
G | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1758+528_1759-124d others(2): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976274 | ||||||
| chr19:16976380
|
G | A | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1759-229C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976380 | ||||||
| chr19:16976454
|
C | A | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1759-303G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976454 | ||||||
| chr19:16976510
|
G | C | 3 | a0002c0059t0001g0044a0004c0014t0002g0222a0004c0014t0002g0223 | 3 | HG02083.hp1 HG02523.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1759-359C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976510 | ||||||
| chr19:16976731
|
T | C | 34 | a0001c0013t0001g0090a0001c0013t0001g0138a0007c0016t0001g0007others(31): Show | 34 | HG00735.hp2 HG01099.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1759-580A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976731 | ||||||
| chr19:16976767
|
C | T | 1 | a0115c0123t0001g0226 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1758+601G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976767 | ||||||
| chr19:16976800
|
G | C | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1758+568C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976800 | ||||||
| chr19:16976860
|
G | A | 138 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1758+508C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976860 | ||||||
| chr19:16976949
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1758+419C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976949 | ||||||
| chr19:16976979
|
T | C | 160 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1758+389A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976979 | ||||||
| chr19:16976991
|
G | A | 1 | a0013c0078t0002g0171 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1758+377C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976991 | ||||||
| chr19:16976997
|
G | A | 153 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1758+371C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16976997 | ||||||
| chr19:16977061
|
T | C | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1758+307A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16977061 | ||||||
| chr19:16977102
|
A | G | 155 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1758+266T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16977102 | ||||||
| chr19:16977144
|
G | C | 155 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1758+224C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16977144 | ||||||
| chr19:16977170
|
C | T | 160 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1758+198G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16977170 | ||||||
| chr19:16977204
|
T | C | 21 | a0001c0013t0001g0090a0001c0013t0001g0138a0007c0016t0001g0007others(18): Show | 21 | HG00735.hp2 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1758+164A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16977204 | ||||||
| chr19:16977311
|
T | C | 156 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1758+57A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | 16977311 | ||||||
| chr19:16977648
|
G | A | 56 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(53): Show | 56 | HG00140.hp2 HG00639.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1586-108C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16977648 | ||||||
| chr19:16977740
|
G | T | 2 | a0047c0046t0002g0135a0047c0046t0002g0136 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1586-200C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16977740 | ||||||
| chr19:16977993
|
G | A | 5 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1586-453C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16977993 | ||||||
| chr19:16978000
|
T | C | 22 | a0001c0013t0001g0090a0001c0013t0001g0138a0007c0016t0001g0007others(19): Show | 22 | HG00735.hp2 HG01099.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1586-460A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978000 | ||||||
| chr19:16978036
|
T | C | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1586-496A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978036 | ||||||
| chr19:16978050
|
A | G | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1586-510T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978050 | ||||||
| chr19:16978080
|
G | A | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1586-540C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978080 | ||||||
| chr19:16978105
|
T | C | 1 | a0069c0098t0001g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1586-565A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978105 | ||||||
| chr19:16978210
|
G | C | 41 | a0001c0013t0001g0090a0001c0013t0001g0138a0007c0016t0001g0007others(38): Show | 41 | HG00735.hp2 HG00741.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1586-670C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978210 | ||||||
| chr19:16978221
|
A | G | 1 | a0033c0040t0001g0265 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1586-681T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978221 | ||||||
| chr19:16978246
|
G | T | 8 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1586-706C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978246 | ||||||
| chr19:16978255
|
T | C | 168 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1586-715A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978255 | ||||||
| chr19:16978566
|
G | A | 163 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1586-1026C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978566 | ||||||
| chr19:16978572
|
A | G | 163 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1586-1032T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978572 | ||||||
| chr19:16978648
|
T | G | 168 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1586-1108A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978648 | ||||||
| chr19:16978748
|
T | A | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1586-1208A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978748 | ||||||
| chr19:16978757
|
C | T | 2 | a0065c0101t0001g0001a0085c0063t0001g0018 | 2 | HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1586-1217G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978757 | ||||||
| chr19:16978817
|
T | C | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1586-1277A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978817 | ||||||
| chr19:16978821
|
C | T | 4 | a0003c0045t0002g0218a0009c0010t0002g0257a0018c0155t0002g0215others(1): Show | 4 | NA18950.hp1 NA19012.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1586-1281G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978821 | ||||||
| chr19:16978968
|
C | T | 169 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1586-1428G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978968 | ||||||
| chr19:16978986
|
A | T | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1586-1446T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978986 | ||||||
| chr19:16978989
|
TATCCATC others(9): Show |
T | 4 | a0023c0031t0001g0025a0023c0031t0001g0026a0029c0067t0001g0004others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1586-1465_1586-145 others(20): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16978989 | ||||||
| chr19:16979206
|
C | T | 2 | a0003c0151t0001g0143a0027c0035t0001g0045 | 2 | HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1585+1291G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979206 | ||||||
| chr19:16979217
|
TATCC | T | 8 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1585+1276_1585+127 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979217 | ||||||
| chr19:16979245
|
T | C | 161 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1585+1252A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979245 | ||||||
| chr19:16979269
|
G | GCCATCCA others(1): Show |
5 | a0034c0070t0002g0091a0042c0174t0001g0160a0092c0173t0001g0164others(2): Show | 5 | HG01109.hp1 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1585+1220_1585+122 others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979269 | ||||||
| chr19:16979269
|
G | GCCATCCA others(5): Show |
147 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1585+1216_1585+122 others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979269 | ||||||
| chr19:16979269
|
G | GCCATCCA others(9): Show |
9 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(6): Show | 9 | HG00741.hp2 HG01884.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1585+1212_1585+122 others(20): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979269 | ||||||
| chr19:16979296
|
C | A | 166 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1585+1201G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979296 | ||||||
| chr19:16979333
|
G | A | 161 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1585+1164C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979333 | ||||||
| chr19:16979344
|
G | T | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1585+1153C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979344 | ||||||
| chr19:16979376
|
A | ATCTGTCC others(180): Show |
1 | a0059c0156t0002g0259 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1585+1120_1585+112 others(191): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979376 | ||||||
| chr19:16979386
|
T | TCATC | 14 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(11): Show | 14 | HG01891.hp2 HG02055.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1585+1107_1585+111 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979386 | ||||||
| chr19:16979386
|
T | TCATCCAT others(1): Show |
114 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1585+1103_1585+111 others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979386 | ||||||
| chr19:16979386
|
T | TCATCCAT others(5): Show |
5 | a0002c0017t0001g0162a0002c0176t0001g0014a0004c0180t0001g0041others(2): Show | 5 | HG02109.hp1 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1585+1099_1585+111 others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979386 | ||||||
| chr19:16979440
|
A | ATCTG | 20 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(17): Show | 20 | HG00741.hp2 HG01884.hp2 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.1585+1056_1585+105 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979440 | ||||||
| chr19:16979440
|
A | G | 143 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1585+1057T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979440 | ||||||
| chr19:16979447
|
A | AATCCACC others(12): Show |
165 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1585+1049_1585+105 others(23): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979447 | ||||||
| chr19:16979474
|
C | T | 5 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1585+1023G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979474 | ||||||
| chr19:16979508
|
G | GTCCA | 142 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1585+985_1585+988d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979508 | ||||||
| chr19:16979531
|
T | C | 1 | a0004c0005t0002g0046 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1585+966A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979531 | ||||||
| chr19:16979551
|
T | C | 165 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1585+946A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979551 | ||||||
| chr19:16979604
|
G | GTCCA | 156 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1585+889_1585+892d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979604 | ||||||
| chr19:16979604
|
G | GTCCATCC others(73): Show |
1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1585+892_1585+893i others(82): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979604 | ||||||
| chr19:16979713
|
G | A | 1 | a0003c0002t0002g0252 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1585+784C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979713 | ||||||
| chr19:16979802
|
C | A | 160 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1585+695G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979802 | ||||||
| chr19:16979818
|
C | CCTGT | 165 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1585+678_1585+679i others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979818 | ||||||
| chr19:16979845
|
G | A | 160 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1585+652C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979845 | ||||||
| chr19:16979942
|
T | C | 1 | a0068c0095t0002g0064 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1585+555A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16979942 | ||||||
| chr19:16980003
|
C | G | 10 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(7): Show | 10 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1585+494G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16980003 | ||||||
| chr19:16980047
|
A | G | 4 | a0016c0116t0001g0010a0016c0117t0001g0114a0028c0114t0001g0100others(1): Show | 4 | HG02055.hp2 HG02809.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1585+450T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16980047 | ||||||
| chr19:16980110
|
A | G | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1585+387T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16980110 | ||||||
| chr19:16980195
|
G | A | 140 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1585+302C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16980195 | ||||||
| chr19:16980279
|
G | A | 2 | a0029c0067t0001g0004a0114c0113t0001g0101 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1585+218C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16980279 | ||||||
| chr19:16980316
|
C | G | 8 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1585+181G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16980316 | ||||||
| chr19:16980319
|
C | T | 17 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(14): Show | 17 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1585+178G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16980319 | ||||||
| chr19:16980331
|
G | T | 142 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1585+166C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16980331 | ||||||
| chr19:16980367
|
G | A | 5 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1585+130C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 14/41 | chr19 | 16980367 | ||||||
| chr19:16980699
|
C | T | 1 | a0064c0161t0002g0187 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1396-13G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16980699 | ||||||
| chr19:16980702
|
A | C | 2 | a0101c0126t0001g0061a0107c0122t0001g0023 | 2 | HG01361.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1396-16T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16980702 | ||||||
| chr19:16980723
|
C | T | 147 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1396-37G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16980723 | ||||||
| chr19:16980752
|
C | T | 5 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-66G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16980752 | ||||||
| chr19:16980759
|
T | G | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-73A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16980759 | ||||||
| chr19:16980796
|
G | A | 2 | a0029c0067t0001g0004a0114c0113t0001g0101 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1396-110C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16980796 | ||||||
| chr19:16980856
|
A | G | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-170T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16980856 | ||||||
| chr19:16980981
|
C | T | 1 | a0003c0002t0002g0252 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1396-295G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16980981 | ||||||
| chr19:16980982
|
G | A | 2 | a0047c0046t0002g0135a0047c0046t0002g0136 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1396-296C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16980982 | ||||||
| chr19:16981031
|
C | T | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-345G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981031 | ||||||
| chr19:16981073
|
C | CAACCACC others(915): Show |
2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-388_1396-387i others(924): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981073 | ||||||
| chr19:16981073
|
C | CAACCACC others(915): Show |
10 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(7): Show | 10 | HG00741.hp2 HG01884.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1396-388_1396-387i others(924): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981073 | ||||||
| chr19:16981077
|
TATTTTG | T | 12 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(9): Show | 12 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-397_1396-392d others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981077 | ||||||
| chr19:16981107
|
CT | C | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-422delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981107 | ||||||
| chr19:16981111
|
G | C | 21 | a0001c0013t0001g0090a0001c0013t0001g0138a0007c0016t0001g0007others(18): Show | 21 | HG00735.hp2 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1396-425C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981111 | ||||||
| chr19:16981156
|
C | A | 1 | a0012c0028t0002g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1396-470G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981156 | ||||||
| chr19:16981170
|
T | C | 1 | a0027c0035t0001g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1396-484A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981170 | ||||||
| chr19:16981222
|
G | A | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1396-536C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981222 | ||||||
| chr19:16981361
|
C | CA | 12 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(9): Show | 12 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-676dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981361 | ||||||
| chr19:16981361
|
C | T | 1 | a0094c0060t0001g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1396-675G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981361 | ||||||
| chr19:16981384
|
C | T | 143 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1396-698G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981384 | ||||||
| chr19:16981525
|
A | G | 12 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(9): Show | 12 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-839T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981525 | ||||||
| chr19:16981607
|
T | C | 1 | a0003c0002t0002g0252 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1396-921A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981607 | ||||||
| chr19:16981652
|
T | C | 1 | a0112c0135t0002g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1396-966A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981652 | ||||||
| chr19:16981750
|
AC | A | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-1065delG | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981750 | ||||||
| chr19:16981824
|
C | A | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-1138G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981824 | ||||||
| chr19:16981825
|
A | T | 1 | a0069c0098t0001g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1396-1139T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981825 | ||||||
| chr19:16981905
|
T | C | 11 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1396-1219A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16981905 | ||||||
| chr19:16982049
|
A | G | 2 | a0029c0067t0001g0004a0114c0113t0001g0101 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1396-1363T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982049 | ||||||
| chr19:16982085
|
G | A | 142 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1396-1399C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982085 | ||||||
| chr19:16982109
|
T | C | 12 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(9): Show | 12 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-1423A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982109 | ||||||
| chr19:16982118
|
C | T | 3 | a0008c0009t0001g0231a0014c0027t0001g0180a0036c0025t0002g0264 | 3 | HG02015.hp1 HG02027.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1396-1432G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982118 | ||||||
| chr19:16982160
|
G | A | 1 | a0059c0156t0002g0259 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1396-1474C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982160 | ||||||
| chr19:16982173
|
T | C | 12 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(9): Show | 12 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-1487A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982173 | ||||||
| chr19:16982189
|
T | C | 12 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(9): Show | 12 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-1503A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982189 | ||||||
| chr19:16982270
|
G | A | 12 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(9): Show | 12 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-1584C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982270 | ||||||
| chr19:16982326
|
G | A | 2 | a0047c0046t0002g0135a0047c0046t0002g0136 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1396-1640C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982326 | ||||||
| chr19:16982458
|
C | T | 6 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-1772G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982458 | ||||||
| chr19:16982461
|
C | T | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-1775G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982461 | ||||||
| chr19:16982462
|
C | G | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-1776G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982462 | ||||||
| chr19:16982705
|
G | A | 2 | a0009c0010t0002g0208a0009c0010t0002g0209 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1396-2019C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982705 | ||||||
| chr19:16982708
|
C | T | 6 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-2022G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982708 | ||||||
| chr19:16982716
|
T | C | 5 | a0016c0185t0001g0058a0028c0181t0002g0060a0028c0182t0001g0062others(2): Show | 5 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-2030A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982716 | ||||||
| chr19:16982733
|
G | A | 5 | a0002c0062t0002g0176a0043c0022t0001g0203a0043c0022t0001g0232others(2): Show | 5 | HG01934.hp2 HG02155.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-2047C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982733 | ||||||
| chr19:16982776
|
C | T | 143 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1396-2090G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982776 | ||||||
| chr19:16982815
|
G | A | 1 | a0008c0150t0001g0273 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1396-2129C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982815 | ||||||
| chr19:16982887
|
C | G | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-2201G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982887 | ||||||
| chr19:16982937
|
A | G | 1 | a0001c0001t0002g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1396-2251T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982937 | ||||||
| chr19:16982981
|
T | G | 1 | a0074c0080t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1396-2295A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982981 | ||||||
| chr19:16982996
|
T | C | 164 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1396-2310A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16982996 | ||||||
| chr19:16983022
|
CTT | C | 3 | a0028c0114t0001g0100a0100c0068t0002g0159a0122c0162t0001g0019 | 3 | HG01891.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1396-2338_1396-233 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983022 | ||||||
| chr19:16983307
|
C | G | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-2621G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983307 | ||||||
| chr19:16983326
|
G | C | 2 | a0029c0067t0001g0004a0114c0113t0001g0101 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1396-2640C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983326 | ||||||
| chr19:16983399
|
A | AAAAT | 6 | a0016c0116t0001g0010a0016c0117t0001g0114a0028c0114t0001g0100others(3): Show | 6 | HG02055.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-2717_1396-271 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983399 | ||||||
| chr19:16983399
|
A | AAAATAAA others(5): Show |
4 | a0065c0101t0001g0001a0085c0063t0001g0018a0086c0179t0001g0102others(1): Show | 4 | HG02451.hp2 HG02559.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-2725_1396-271 others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983399 | ||||||
| chr19:16983399
|
A | AAAATAAA others(9): Show |
2 | a0083c0112t0001g0096a0084c0111t0001g0097 | 2 | HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1396-2729_1396-271 others(20): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983399 | ||||||
| chr19:16983399
|
AAAAT | A | 150 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1396-2717_1396-271 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983399 | ||||||
| chr19:16983399
|
AAAATAAA others(1): Show |
A | 4 | a0047c0046t0002g0135a0047c0046t0002g0136a0100c0068t0002g0159others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-2721_1396-271 others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983399 | ||||||
| chr19:16983465
|
G | A | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-2779C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983465 | ||||||
| chr19:16983584
|
C | T | 4 | a0002c0019t0001g0008a0002c0019t0001g0139a0100c0068t0002g0159others(1): Show | 4 | HG01891.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-2898G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983584 | ||||||
| chr19:16983607
|
A | C | 5 | a0016c0185t0001g0058a0028c0181t0002g0060a0028c0182t0001g0062others(2): Show | 5 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-2921T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983607 | ||||||
| chr19:16983771
|
T | C | 5 | a0020c0011t0001g0017a0020c0011t0001g0020a0020c0011t0001g0021others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-3085A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983771 | ||||||
| chr19:16983855
|
G | C | 6 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-3169C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983855 | ||||||
| chr19:16983856
|
A | G | 3 | a0001c0001t0002g0048a0001c0007t0002g0053a0079c0085t0001g0047 | 3 | HG00609.hp2 NA18949.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1396-3170T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983856 | ||||||
| chr19:16983867
|
A | G | 1 | a0025c0020t0001g0153 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1396-3181T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983867 | ||||||
| chr19:16983919
|
A | G | 219 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1396-3233T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983919 | ||||||
| chr19:16983980
|
T | C | 1 | a0052c0152t0002g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1396-3294A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16983980 | ||||||
| chr19:16984014
|
G | A | 217 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1396-3328C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984014 | ||||||
| chr19:16984145
|
G | A | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-3459C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984145 | ||||||
| chr19:16984147
|
A | G | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-3461T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984147 | ||||||
| chr19:16984274
|
A | C | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-3588T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984274 | ||||||
| chr19:16984313
|
C | CA | 6 | a0008c0009t0001g0197a0021c0037t0002g0190a0029c0067t0001g0004others(3): Show | 6 | HG02015.hp2 HG02055.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-3628dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984313 | ||||||
| chr19:16984330
|
A | G | 1 | a0005c0003t0002g0244 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1396-3644T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984330 | ||||||
| chr19:16984330
|
AAG | A | 29 | a0001c0013t0001g0090a0001c0013t0001g0138a0004c0180t0001g0041others(26): Show | 29 | HG00735.hp2 HG01099.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1396-3646_1396-364 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984330 | ||||||
| chr19:16984331
|
AG | A | 58 | a0001c0001t0002g0185a0002c0017t0001g0112a0002c0017t0001g0113others(55): Show | 58 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1396-3646delC | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984331 | ||||||
| chr19:16984331
|
AGAGAG | A | 9 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(6): Show | 9 | HG00741.hp2 HG01884.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1396-3650_1396-364 others(9): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984331 | ||||||
| chr19:16984332
|
G | A | 65 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1396-3646C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984332 | ||||||
| chr19:16984334
|
G | A | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-3648C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984334 | ||||||
| chr19:16984336
|
G | A | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-3650C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984336 | ||||||
| chr19:16984392
|
TAACTC | T | 14 | a0001c0013t0001g0090a0001c0013t0001g0138a0010c0004t0001g0068others(11): Show | 14 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1396-3711_1396-370 others(9): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984392 | ||||||
| chr19:16984441
|
C | G | 10 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(7): Show | 10 | HG00741.hp2 HG01884.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1396-3755G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984441 | ||||||
| chr19:16984477
|
A | G | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-3791T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984477 | ||||||
| chr19:16984510
|
C | T | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-3824G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984510 | ||||||
| chr19:16984687
|
G | A | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-4001C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984687 | ||||||
| chr19:16984704
|
C | G | 2 | a0047c0046t0002g0135a0047c0046t0002g0136 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1396-4018G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984704 | ||||||
| chr19:16984721
|
G | C | 1 | a0029c0137t0002g0270 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1396-4035C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984721 | ||||||
| chr19:16984779
|
C | T | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-4093G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984779 | ||||||
| chr19:16984838
|
C | T | 1 | a0002c0176t0001g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1396-4152G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984838 | ||||||
| chr19:16984900
|
C | T | 10 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(7): Show | 10 | HG00741.hp2 HG01884.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1396-4214G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984900 | ||||||
| chr19:16984908
|
T | A | 1 | a0044c0021t0002g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1396-4222A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16984908 | ||||||
| chr19:16985078
|
T | C | 2 | a0029c0067t0001g0004a0114c0113t0001g0101 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1396-4392A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985078 | ||||||
| chr19:16985153
|
T | C | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1396-4467A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985153 | ||||||
| chr19:16985247
|
T | C | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1395+4396A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985247 | ||||||
| chr19:16985342
|
C | CGGAT | 24 | a0001c0013t0001g0090a0001c0013t0001g0138a0007c0016t0001g0007others(21): Show | 24 | HG00735.hp2 HG00741.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1395+4297_1395+430 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985342 | ||||||
| chr19:16985342
|
C | CGGATGGA others(5): Show |
2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1395+4300_1395+430 others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985342 | ||||||
| chr19:16985342
|
C | CGGATGGA others(5): Show |
15 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(12): Show | 15 | HG01884.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1395+4289_1395+430 others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985342 | ||||||
| chr19:16985342
|
C | CGGATGGA others(9): Show |
109 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.1395+4285_1395+430 others(20): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985342 | ||||||
| chr19:16985342
|
C | CGGATGGA others(13): Show |
16 | a0002c0176t0001g0014a0004c0014t0002g0038a0011c0012t0002g0210others(13): Show | 16 | HG01109.hp1 HG01361.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1395+4281_1395+430 others(24): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985342 | ||||||
| chr19:16985366
|
G | T | 2 | a0047c0046t0002g0135a0047c0046t0002g0136 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1395+4277C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985366 | ||||||
| chr19:16985442
|
G | A | 1 | a0029c0137t0002g0270 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1395+4201C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985442 | ||||||
| chr19:16985450
|
AGATG | A | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+4189_1395+419 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985450 | ||||||
| chr19:16985457
|
T | C | 1 | a0011c0090t0001g0255 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1395+4186A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985457 | ||||||
| chr19:16985610
|
TGATG | T | 10 | a0005c0003t0002g0166a0006c0006t0001g0086a0006c0006t0001g0131others(7): Show | 10 | HG00735.hp1 HG01081.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395+4029_1395+403 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985610 | ||||||
| chr19:16985631
|
C | T | 1 | a0015c0008t0001g0005 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1395+4012G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985631 | ||||||
| chr19:16985632
|
G | A | 1 | a0004c0005t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1395+4011C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985632 | ||||||
| chr19:16985792
|
A | G | 1 | a0038c0109t0002g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1395+3851T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985792 | ||||||
| chr19:16985833
|
G | C | 1 | a0011c0091t0001g0179 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1395+3810C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985833 | ||||||
| chr19:16985906
|
A | C | 1 | a0093c0177t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1395+3737T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985906 | ||||||
| chr19:16985931
|
A | C | 2 | a0003c0002t0002g0213a0009c0042t0001g0206 | 2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1395+3712T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16985931 | ||||||
| chr19:16986007
|
T | C | 1 | a0007c0170t0002g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1395+3636A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986007 | ||||||
| chr19:16986100
|
C | A | 2 | a0001c0001t0002g0199a0021c0037t0002g0190 | 2 | HG03710.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1395+3543G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986100 | ||||||
| chr19:16986138
|
G | A | 6 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+3505C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986138 | ||||||
| chr19:16986181
|
C | T | 6 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+3462G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986181 | ||||||
| chr19:16986182
|
G | A | 3 | a0030c0166t0002g0059a0030c0167t0001g0271a0048c0168t0001g0272 | 3 | HG02145.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1395+3461C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986182 | ||||||
| chr19:16986193
|
G | A | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+3450C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986193 | ||||||
| chr19:16986263
|
T | C | 2 | a0029c0067t0001g0004a0114c0113t0001g0101 | 2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1395+3380A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986263 | ||||||
| chr19:16986281
|
G | A | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1395+3362C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986281 | ||||||
| chr19:16986478
|
C | T | 3 | a0001c0001t0002g0147a0024c0030t0001g0148a0024c0030t0001g0173 | 3 | NA18947.hp2 NA19011.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1395+3165G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986478 | ||||||
| chr19:16986566
|
C | A | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1395+3077G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986566 | ||||||
| chr19:16986609
|
C | A | 2 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1395+3034G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986609 | ||||||
| chr19:16986660
|
G | A | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+2983C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986660 | ||||||
| chr19:16986688
|
G | C | 1 | a0007c0052t0002g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1395+2955C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986688 | ||||||
| chr19:16986788
|
C | T | 1 | a0114c0113t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1395+2855G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986788 | ||||||
| chr19:16986841
|
G | A | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1395+2802C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986841 | ||||||
| chr19:16986884
|
G | A | 6 | a0065c0101t0001g0001a0083c0112t0001g0096a0084c0111t0001g0097others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+2759C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16986884 | ||||||
| chr19:16987072
|
G | T | 9 | a0021c0143t0001g0012a0023c0075t0001g0137a0039c0076t0001g0126others(6): Show | 9 | HG00741.hp2 HG01884.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395+2571C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987072 | ||||||
| chr19:16987152
|
C | CA | 11 | a0005c0003t0002g0239a0006c0006t0001g0086a0006c0006t0001g0131others(8): Show | 11 | HG00609.hp1 HG01081.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1395+2490dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987152 | ||||||
| chr19:16987152
|
C | CAA | 8 | a0006c0006t0001g0220a0013c0024t0002g0275a0015c0008t0001g0035others(5): Show | 8 | HG01192.hp1 HG01515.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395+2489_1395+249 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987152 | ||||||
| chr19:16987152
|
C | CAAA | 6 | a0014c0105t0001g0140a0022c0032t0001g0228a0022c0032t0001g0229others(3): Show | 6 | HG02027.hp1 HG02135.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+2488_1395+249 others(7): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987152 | ||||||
| chr19:16987152
|
CA | C | 10 | a0002c0018t0001g0115a0003c0002t0002g0196a0005c0131t0002g0063others(7): Show | 10 | HG01978.hp2 HG02083.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395+2490delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987152 | ||||||
| chr19:16987152
|
CAAAA | C | 17 | a0002c0017t0001g0113a0002c0018t0001g0099a0002c0018t0001g0116others(14): Show | 17 | HG00140.hp2 HG01109.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.1395+2487_1395+249 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987152 | ||||||
| chr19:16987166
|
AAAAAAAA others(8): Show |
A | 1 | a0004c0005t0002g0042 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1395+2462_1395+247 others(19): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987166 | ||||||
| chr19:16987166
|
AAAAAAAA others(14): Show |
A | 5 | a0016c0185t0001g0058a0028c0181t0002g0060a0028c0182t0001g0062others(2): Show | 5 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+2456_1395+247 others(25): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987166 | ||||||
| chr19:16987171
|
A | T | 2 | a0040c0074t0002g0212a0082c0165t0002g0214 | 2 | HG01516.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1395+2472T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987171 | ||||||
| chr19:16987172
|
AAAAAAAA others(6): Show |
A | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1395+2458_1395+247 others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987172 | ||||||
| chr19:16987173
|
A | AATATATA others(15): Show |
1 | a0041c0023t0002g0258 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1395+2469_1395+247 others(26): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987173 | ||||||
| chr19:16987173
|
A | T | 3 | a0004c0180t0001g0041a0040c0074t0002g0212a0082c0165t0002g0214 | 3 | HG01516.hp2 NA18971.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1395+2470T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987173 | ||||||
| chr19:16987174
|
AAAAAAAT others(4): Show |
A | 1 | a0005c0003t0002g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1395+2458_1395+246 others(15): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987174 | ||||||
| chr19:16987175
|
A | T | 8 | a0004c0180t0001g0041a0006c0006t0001g0183a0008c0150t0001g0273others(5): Show | 8 | HG01168.hp2 HG01516.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395+2468T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987175 | ||||||
| chr19:16987177
|
A | AATATATA others(15): Show |
1 | a0124c0186t0001g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1395+2465_1395+246 others(26): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987177 | ||||||
| chr19:16987177
|
A | ATATATAT others(8): Show |
2 | a0010c0004t0001g0068a0069c0098t0001g0065 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1395+2465_1395+246 others(19): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987177 | ||||||
| chr19:16987177
|
A | ATATATAT others(10): Show |
1 | a0045c0051t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1395+2465_1395+246 others(21): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987177 | ||||||
| chr19:16987177
|
A | ATATATAT others(12): Show |
1 | a0123c0048t0001g0011 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1395+2465_1395+246 others(23): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987177 | ||||||
| chr19:16987177
|
A | T | 16 | a0002c0018t0001g0099a0002c0018t0001g0115a0004c0180t0001g0041others(13): Show | 16 | HG01168.hp2 HG01515.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.1395+2466T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987177 | ||||||
| chr19:16987178
|
AAATATAT | A | 10 | a0001c0001t0002g0048a0010c0004t0001g0088a0011c0012t0002g0207others(7): Show | 10 | HG00609.hp2 HG01070.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395+2458_1395+246 others(11): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987178 | ||||||
| chr19:16987179
|
A | AAAAAAAA others(11): Show |
1 | a0074c0080t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(22): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAAAAAAA others(9): Show |
1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(20): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAAAATAT others(4): Show |
1 | a0005c0003t0002g0125 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(15): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAAAATAT others(6): Show |
1 | a0040c0141t0002g0245 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAAAATAT others(10): Show |
1 | a0073c0082t0001g0069 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(21): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAAATATA others(3): Show |
3 | a0033c0040t0001g0265a0083c0112t0001g0096a0087c0178t0001g0103 | 3 | HG00642.hp2 HG02559.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1395+2463_1395+246 others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAAATATA others(11): Show |
1 | a0001c0013t0001g0138 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(22): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAAATATA others(17): Show |
1 | a0041c0023t0002g0157 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(28): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAATATAT others(6): Show |
1 | a0081c0079t0001g0080 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAATATAT others(8): Show |
1 | a0117c0110t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(19): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAATATAT others(12): Show |
1 | a0007c0016t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(23): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AAATATAT others(16): Show |
1 | a0072c0081t0001g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(27): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AATATATA others(7): Show |
1 | a0047c0046t0002g0136 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1395+2450_1395+246 others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | AT | 3 | a0003c0002t0002g0200a0003c0002t0002g0252a0009c0010t0002g0078 | 3 | HG00423.hp1 HG02074.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1395+2463_1395+246 others(5): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | ATATATAT others(6): Show |
1 | a0047c0046t0002g0135 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | ATATATAT others(14): Show |
1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1395+2463_1395+246 others(25): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
A | T | 37 | a0002c0017t0001g0112a0002c0018t0001g0099a0002c0018t0001g0115others(34): Show | 37 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.1395+2464T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
AATAT | A | 6 | a0002c0017t0001g0162a0004c0100t0002g0054a0009c0010t0002g0208others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395+2460_1395+246 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
AATATAT | A | 30 | a0001c0001t0002g0147a0001c0001t0002g0199a0001c0001t0002g0219others(27): Show | 30 | HG00099.hp2 HG00438.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.1395+2458_1395+246 others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987179
|
AATATATA others(3): Show |
A | 5 | a0020c0011t0001g0020a0020c0011t0001g0021a0034c0071t0001g0070others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+2454_1395+246 others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987179 | ||||||
| chr19:16987180
|
AT | A | 6 | a0013c0024t0002g0178a0015c0008t0001g0174a0032c0043t0001g0037others(3): Show | 6 | HG01168.hp1 HG01496.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395+2462delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987180 | ||||||
| chr19:16987180
|
ATATAT | A | 10 | a0001c0033t0002g0002a0002c0176t0001g0014a0004c0005t0002g0188others(7): Show | 10 | HG00438.hp2 HG00741.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1395+2458_1395+246 others(9): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987180 | ||||||
| chr19:16987180
|
ATATATAT | A | 10 | a0001c0001t0002g0185a0007c0016t0001g0123a0007c0016t0001g0124others(7): Show | 10 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1395+2456_1395+246 others(11): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987180 | ||||||
| chr19:16987181
|
T | A | 39 | a0001c0102t0002g0079a0003c0002t0002g0039a0003c0151t0001g0143others(36): Show | 39 | HG00140.hp1 HG00639.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1395+2462A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987181 | ||||||
| chr19:16987183
|
T | A | 20 | a0005c0003t0002g0239a0005c0121t0002g0267a0006c0006t0001g0086others(17): Show | 20 | HG01081.hp1 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1395+2460A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987183 | ||||||
| chr19:16987185
|
T | A | 11 | a0002c0017t0001g0162a0004c0100t0002g0054a0006c0006t0001g0086others(8): Show | 11 | HG01081.hp1 HG01192.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.1395+2458A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987185 | ||||||
| chr19:16987187
|
T | A | 22 | a0001c0001t0002g0147a0001c0001t0002g0199a0001c0001t0002g0219others(19): Show | 22 | HG00438.hp1 HG01256.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.1395+2456A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987187 | ||||||
| chr19:16987189
|
T | A | 5 | a0004c0005t0002g0146a0011c0090t0001g0255a0012c0029t0001g0151others(2): Show | 5 | HG02040.hp2 HG02559.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+2454A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987189 | ||||||
| chr19:16987190
|
A | ATATATAT others(17): Show |
1 | a0040c0074t0002g0212 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1395+2452_1395+245 others(28): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987190 | ||||||
| chr19:16987191
|
T | A | 5 | a0020c0011t0001g0017a0020c0011t0001g0020a0020c0011t0001g0021others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+2452A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987191 | ||||||
| chr19:16987193
|
T | A | 4 | a0020c0011t0001g0017a0020c0011t0001g0020a0020c0011t0001g0021others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395+2450A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987193 | ||||||
| chr19:16987319
|
A | T | 10 | a0004c0180t0001g0041a0016c0050t0001g0095a0016c0116t0001g0010others(7): Show | 10 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1395+2324T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987319 | ||||||
| chr19:16987326
|
T | C | 1 | a0005c0003t0002g0167 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1395+2317A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987326 | ||||||
| chr19:16987513
|
G | A | 42 | a0001c0013t0001g0090a0001c0013t0001g0138a0003c0002t0002g0105others(39): Show | 42 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1395+2130C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987513 | ||||||
| chr19:16987566
|
T | G | 1 | a0001c0001t0002g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1395+2077A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987566 | ||||||
| chr19:16987570
|
G | T | 19 | a0001c0013t0001g0090a0001c0013t0001g0138a0007c0016t0001g0007others(16): Show | 19 | HG00735.hp2 HG01099.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.1395+2073C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987570 | ||||||
| chr19:16987627
|
C | A | 1 | a0006c0015t0002g0263 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1395+2016G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987627 | ||||||
| chr19:16987682
|
G | A | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1395+1961C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987682 | ||||||
| chr19:16987744
|
G | A | 1 | a0008c0160t0001g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1395+1899C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987744 | ||||||
| chr19:16987819
|
G | T | 1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1395+1824C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987819 | ||||||
| chr19:16987888
|
T | C | 1 | a0089c0065t0002g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1395+1755A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16987888 | ||||||
| chr19:16988184
|
G | C | 2 | a0029c0067t0001g0004a0122c0162t0001g0019 | 2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1395+1459C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988184 | ||||||
| chr19:16988373
|
G | A | 1 | a0033c0040t0001g0043 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1395+1270C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988373 | ||||||
| chr19:16988553
|
T | C | 2 | a0005c0121t0002g0267a0112c0135t0002g0268 | 2 | HG00639.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1395+1090A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988553 | ||||||
| chr19:16988621
|
A | T | 1 | a0001c0007t0002g0036 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1395+1022T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988621 | ||||||
| chr19:16988767
|
A | C | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1395+876T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988767 | ||||||
| chr19:16988785
|
C | T | 2 | a0047c0046t0002g0135a0047c0046t0002g0136 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1395+858G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988785 | ||||||
| chr19:16988828
|
T | C | 225 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1395+815A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988828 | ||||||
| chr19:16988859
|
C | T | 50 | a0003c0002t0002g0105a0005c0003t0002g0051a0005c0003t0002g0125others(47): Show | 50 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1395+784G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988859 | ||||||
| chr19:16988864
|
G | A | 1 | a0040c0141t0002g0245 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1395+779C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988864 | ||||||
| chr19:16988930
|
T | A | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1395+713A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988930 | ||||||
| chr19:16988971
|
T | A | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1395+672A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16988971 | ||||||
| chr19:16989170
|
G | A | 160 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1395+473C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16989170 | ||||||
| chr19:16989204
|
C | T | 1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1395+439G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16989204 | ||||||
| chr19:16989213
|
G | A | 1 | a0011c0012t0002g0202 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1395+430C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16989213 | ||||||
| chr19:16989226
|
T | C | 23 | a0001c0013t0001g0090a0001c0013t0001g0138a0004c0180t0001g0041others(20): Show | 23 | HG00735.hp2 HG01099.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.1395+417A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16989226 | ||||||
| chr19:16989411
|
C | T | 1 | a0008c0009t0001g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1395+232G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16989411 | ||||||
| chr19:16989520
|
C | A | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1395+123G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16989520 | ||||||
| chr19:16989567
|
A | T | 25 | a0001c0013t0001g0090a0001c0013t0001g0138a0004c0180t0001g0041others(22): Show | 25 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1395+76T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16989567 | ||||||
| chr19:16989603
|
T | A | 1 | a0019c0039t0001g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1395+40A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16989603 | ||||||
| chr19:16989618
|
G | C | 1 | a0101c0126t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1395+25C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16989618 | ||||||
| chr19:16989628
|
T | A | 170 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1395+15A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 13/41 | chr19 | 16989628 | ||||||
| chr19:16989791
|
A | G | 6 | a0016c0185t0001g0058a0028c0181t0002g0060a0028c0182t0001g0062others(3): Show | 6 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267-20T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16989791 | ||||||
| chr19:16989856
|
G | GA | 11 | a0021c0143t0001g0012a0039c0076t0001g0126a0055c0145t0001g0093others(8): Show | 11 | HG00741.hp2 HG01884.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1267-86dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16989856 | ||||||
| chr19:16989921
|
A | G | 52 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0120t0001g0074others(49): Show | 52 | HG00735.hp2 HG00741.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1267-150T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16989921 | ||||||
| chr19:16990009
|
C | T | 6 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1267-238G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990009 | ||||||
| chr19:16990115
|
G | T | 6 | a0020c0011t0001g0017a0020c0011t0001g0020a0020c0011t0001g0021others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267-344C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990115 | ||||||
| chr19:16990123
|
G | T | 6 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1267-352C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990123 | ||||||
| chr19:16990243
|
ACT | A | 3 | a0030c0166t0002g0059a0030c0167t0001g0271a0048c0168t0001g0272 | 3 | HG02145.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1267-474_1267-473d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990243 | ||||||
| chr19:16990343
|
A | G | 1 | a0008c0160t0001g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1267-572T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990343 | ||||||
| chr19:16990376
|
G | A | 1 | a0109c0184t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1267-605C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990376 | ||||||
| chr19:16990525
|
C | A | 2 | a0083c0112t0001g0096a0084c0111t0001g0097 | 2 | HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1267-754G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990525 | ||||||
| chr19:16990593
|
G | A | 107 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1267-822C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990593 | ||||||
| chr19:16990612
|
C | A | 2 | a0002c0120t0001g0074a0045c0118t0001g0024 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1267-841G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990612 | ||||||
| chr19:16990753
|
C | T | 1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1267-982G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990753 | ||||||
| chr19:16990832
|
C | T | 2 | a0047c0046t0002g0135a0047c0046t0002g0136 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1267-1061G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990832 | ||||||
| chr19:16990863
|
C | CA | 27 | a0002c0017t0001g0162a0002c0058t0002g0149a0003c0002t0002g0039others(24): Show | 27 | HG00140.hp2 HG00741.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1267-1093dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
C | CAAAAAAA others(3): Show |
3 | a0002c0120t0001g0074a0045c0118t0001g0024a0112c0135t0002g0268 | 3 | HG00639.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1267-1102_1267-109 others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
C | CAAAAAAA others(4): Show |
18 | a0005c0003t0002g0166a0005c0003t0002g0167a0005c0003t0002g0236others(15): Show | 18 | HG01070.hp1 HG01081.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.1267-1103_1267-109 others(15): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
C | CAAAAAAA others(5): Show |
12 | a0005c0003t0002g0051a0005c0131t0002g0063a0006c0006t0001g0220others(9): Show | 12 | HG01192.hp1 HG01515.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1267-1104_1267-109 others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
C | CAAAAAAA others(6): Show |
3 | a0029c0125t0002g0034a0102c0130t0002g0030a0106c0134t0001g0109 | 3 | NA18959.hp2 NA18992.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1267-1105_1267-109 others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
C | CAAAAAAA others(7): Show |
1 | a0113c0136t0002g0169 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1267-1106_1267-109 others(18): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
C | CAAAAAAA others(8): Show |
4 | a0006c0015t0002g0110a0108c0183t0001g0056a0109c0184t0001g0057others(1): Show | 4 | HG01975.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1267-1107_1267-109 others(19): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
C | CAAAAAAA others(9): Show |
4 | a0016c0185t0001g0058a0028c0182t0001g0062a0100c0068t0002g0159others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1267-1108_1267-109 others(20): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
CA | C | 7 | a0002c0017t0001g0112a0002c0017t0001g0113a0003c0002t0002g0196others(4): Show | 7 | HG01167.hp1 HG01978.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1267-1093delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0002g0277a0010c0004t0001g0089a0010c0004t0001g0254others(4): Show | 7 | HG01099.hp2 HG01109.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1267-1100_1267-109 others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
CAAAAAAA others(2): Show |
C | 97 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0001t0002g0185others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.1267-1101_1267-109 others(13): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990863
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0002g0147a0001c0007t0002g0246a0037c0093t0001g0274 | 3 | HG01256.hp1 HG02132.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1267-1102_1267-109 others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990863 | ||||||
| chr19:16990952
|
C | T | 1 | a0112c0135t0002g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1267-1181G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16990952 | ||||||
| chr19:16991106
|
CAA | C | 103 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1267-1337_1267-133 others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991106 | ||||||
| chr19:16991182
|
G | A | 1 | a0016c0117t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1267-1411C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991182 | ||||||
| chr19:16991402
|
T | G | 1 | a0117c0110t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1267-1631A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991402 | ||||||
| chr19:16991485
|
T | A | 2 | a0007c0016t0001g0123a0007c0016t0001g0124 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1267-1714A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991485 | ||||||
| chr19:16991641
|
G | A | 5 | a0001c0001t0002g0276a0013c0024t0002g0178a0013c0024t0002g0275others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1266+1775C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991641 | ||||||
| chr19:16991681
|
C | A | 48 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(45): Show | 48 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.1266+1735G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991681 | ||||||
| chr19:16991787
|
C | T | 1 | a0117c0110t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1266+1629G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991787 | ||||||
| chr19:16991854
|
C | A | 2 | a0011c0012t0002g0210a0071c0097t0001g0182 | 2 | NA19000.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1266+1562G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991854 | ||||||
| chr19:16991854
|
C | CA | 101 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1266+1561dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991854 | ||||||
| chr19:16991854
|
C | CAAAA | 6 | a0005c0121t0002g0267a0008c0160t0001g0040a0027c0035t0001g0045others(3): Show | 6 | HG01081.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1266+1558_1266+156 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991854 | ||||||
| chr19:16991854
|
CA | C | 15 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(12): Show | 15 | HG00639.hp2 HG01361.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266+1561delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991854 | ||||||
| chr19:16991963
|
A | G | 218 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1266+1453T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16991963 | ||||||
| chr19:16992074
|
G | A | 1 | a0060c0157t0002g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1266+1342C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992074 | ||||||
| chr19:16992076
|
C | T | 3 | a0015c0008t0001g0174a0027c0035t0001g0172a0113c0136t0002g0169 | 3 | HG01516.hp1 HG03490.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1266+1340G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992076 | ||||||
| chr19:16992129
|
C | A | 48 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(45): Show | 48 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.1266+1287G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992129 | ||||||
| chr19:16992246
|
G | A | 6 | a0016c0185t0001g0058a0028c0181t0002g0060a0028c0182t0001g0062others(3): Show | 6 | HG01361.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266+1170C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992246 | ||||||
| chr19:16992377
|
T | G | 54 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(51): Show | 54 | HG00140.hp2 HG00642.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.1266+1039A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992377 | ||||||
| chr19:16992497
|
G | C | 1 | a0027c0035t0001g0045 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1266+919C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992497 | ||||||
| chr19:16992512
|
C | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1266+904G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992512 | ||||||
| chr19:16992531
|
G | A | 217 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1266+885C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992531 | ||||||
| chr19:16992795
|
C | T | 1 | a0019c0039t0001g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1266+621G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992795 | ||||||
| chr19:16992932
|
TA | T | 11 | a0003c0002t0002g0186a0003c0045t0002g0052a0008c0150t0001g0273others(8): Show | 11 | HG01168.hp1 HG01168.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1266+483delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992932 | ||||||
| chr19:16992991
|
G | A | 1 | a0117c0110t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1266+425C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16992991 | ||||||
| chr19:16993001
|
G | A | 2 | a0007c0053t0001g0156a0099c0054t0001g0003 | 2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1266+415C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16993001 | ||||||
| chr19:16993048
|
A | G | 3 | a0007c0052t0002g0119a0007c0053t0001g0156a0099c0054t0001g0003 | 3 | HG02486.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1266+368T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16993048 | ||||||
| chr19:16993113
|
C | G | 7 | a0021c0143t0001g0012a0055c0145t0001g0093a0061c0142t0002g0015others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1266+303G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16993113 | ||||||
| chr19:16993316
|
G | A | 2 | a0006c0015t0002g0133a0006c0015t0002g0263 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1266+100C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16993316 | ||||||
| chr19:16993319
|
C | T | 2 | a0083c0112t0001g0096a0084c0111t0001g0097 | 2 | HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1266+97G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16993319 | ||||||
| chr19:16993352
|
C | T | 46 | a0005c0003t0002g0051a0005c0003t0002g0125a0005c0003t0002g0166others(43): Show | 46 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1266+64G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16993352 | ||||||
| chr19:16993355
|
G | C | 1 | a0005c0003t0002g0051 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1266+61C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 12/41 | chr19 | 16993355 | ||||||
| chr19:16993624
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1096-38C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16993624 | ||||||
| chr19:16993860
|
G | A | 8 | a0020c0011t0001g0017a0020c0011t0001g0020a0020c0011t0001g0021others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1096-274C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16993860 | ||||||
| chr19:16994061
|
C | T | 6 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1096-475G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994061 | ||||||
| chr19:16994082
|
G | A | 8 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(5): Show | 8 | HG02055.hp2 HG02559.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-496C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994082 | ||||||
| chr19:16994170
|
A | G | 1 | a0008c0160t0001g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1096-584T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994170 | ||||||
| chr19:16994247
|
T | C | 47 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(44): Show | 47 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.1096-661A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994247 | ||||||
| chr19:16994385
|
C | G | 93 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1096-799G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994385 | ||||||
| chr19:16994470
|
G | A | 2 | a0002c0120t0001g0074a0045c0118t0001g0024 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1096-884C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994470 | ||||||
| chr19:16994515
|
C | CT | 121 | a0001c0001t0002g0048a0001c0001t0002g0185a0001c0001t0002g0199others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1096-930dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994515 | ||||||
| chr19:16994515
|
C | CTT | 15 | a0004c0005t0002g0046a0005c0121t0002g0267a0011c0012t0002g0210others(12): Show | 15 | HG00639.hp2 HG01109.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1096-931_1096-930d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994515 | ||||||
| chr19:16994515
|
C | CTTT | 45 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(42): Show | 45 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.1096-932_1096-930d others(5): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994515 | ||||||
| chr19:16994515
|
C | CTTTT | 6 | a0002c0056t0001g0081a0007c0119t0001g0122a0008c0160t0001g0040others(3): Show | 6 | HG02698.hp1 HG02886.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096-933_1096-930d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994515 | ||||||
| chr19:16994515
|
CT | C | 8 | a0008c0009t0001g0217a0008c0150t0001g0273a0009c0010t0002g0208others(5): Show | 8 | HG01168.hp2 HG01256.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-930delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994515 | ||||||
| chr19:16994620
|
G | A | 2 | a0003c0002t0002g0213a0009c0042t0001g0206 | 2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1096-1034C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994620 | ||||||
| chr19:16994635
|
C | T | 1 | a0039c0076t0001g0126 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1096-1049G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994635 | ||||||
| chr19:16994688
|
T | A | 8 | a0020c0011t0001g0017a0020c0011t0001g0020a0020c0011t0001g0021others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1096-1102A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994688 | ||||||
| chr19:16994688
|
TA | T | 216 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1096-1103delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994688 | ||||||
| chr19:16994690
|
A | T | 7 | a0005c0121t0002g0267a0008c0160t0001g0040a0027c0035t0001g0045others(4): Show | 7 | HG00735.hp2 HG01081.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-1104T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994690 | ||||||
| chr19:16994787
|
G | A | 1 | a0117c0110t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1096-1201C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994787 | ||||||
| chr19:16994866
|
C | A | 2 | a0007c0053t0001g0156a0099c0054t0001g0003 | 2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1096-1280G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994866 | ||||||
| chr19:16994997
|
G | A | 1 | a0021c0143t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1096-1411C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16994997 | ||||||
| chr19:16995020
|
C | T | 6 | a0027c0035t0001g0045a0040c0074t0002g0212a0040c0141t0002g0245others(3): Show | 6 | HG01081.hp2 HG01099.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1096-1434G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995020 | ||||||
| chr19:16995254
|
G | C | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1096-1668C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995254 | ||||||
| chr19:16995412
|
T | C | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1095+1699A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995412 | ||||||
| chr19:16995424
|
C | T | 1 | a0056c0072t0001g0094 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1095+1687G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995424 | ||||||
| chr19:16995429
|
TCTCA | T | 51 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(48): Show | 51 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.1095+1678_1095+168 others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995429 | ||||||
| chr19:16995621
|
G | A | 1 | a0080c0089t0002g0250 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1095+1490C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995621 | ||||||
| chr19:16995719
|
A | T | 2 | a0001c0001t0002g0248a0010c0004t0001g0254 | 2 | HG00099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1095+1392T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995719 | ||||||
| chr19:16995860
|
A | T | 97 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1095+1251T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995860 | ||||||
| chr19:16995872
|
A | C | 1 | a0027c0035t0001g0045 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1095+1239T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995872 | ||||||
| chr19:16995873
|
G | A | 1 | a0027c0035t0001g0045 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1095+1238C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995873 | ||||||
| chr19:16995978
|
C | T | 4 | a0008c0160t0001g0040a0029c0067t0001g0004a0047c0046t0002g0135others(1): Show | 4 | HG02698.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+1133G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16995978 | ||||||
| chr19:16996112
|
T | C | 1 | a0007c0052t0002g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1095+999A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996112 | ||||||
| chr19:16996137
|
G | A | 4 | a0008c0160t0001g0040a0029c0067t0001g0004a0047c0046t0002g0135others(1): Show | 4 | HG02698.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+974C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996137 | ||||||
| chr19:16996396
|
T | C | 6 | a0004c0005t0002g0188a0004c0005t0002g0211a0011c0012t0002g0210others(3): Show | 6 | HG00423.hp2 HG00597.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+715A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996396 | ||||||
| chr19:16996519
|
A | G | 1 | a0122c0162t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1095+592T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996519 | ||||||
| chr19:16996587
|
G | A | 12 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(9): Show | 12 | HG01361.hp1 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+524C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996587 | ||||||
| chr19:16996660
|
A | G | 7 | a0021c0143t0001g0012a0055c0145t0001g0093a0061c0142t0002g0015others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1095+451T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996660 | ||||||
| chr19:16996681
|
T | A | 4 | a0008c0160t0001g0040a0029c0067t0001g0004a0047c0046t0002g0135others(1): Show | 4 | HG02698.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+430A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996681 | ||||||
| chr19:16996727
|
G | A | 1 | a0006c0006t0001g0086 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1095+384C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996727 | ||||||
| chr19:16996797
|
C | T | 1 | a0008c0009t0001g0247 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1095+314G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996797 | ||||||
| chr19:16996804
|
G | T | 1 | a0045c0051t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1095+307C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996804 | ||||||
| chr19:16996806
|
G | A | 15 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(12): Show | 15 | HG00741.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1095+305C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996806 | ||||||
| chr19:16996816
|
C | T | 1 | a0003c0002t0002g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1095+295G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996816 | ||||||
| chr19:16996817
|
TA | T | 200 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1095+293delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996817 | ||||||
| chr19:16996817
|
TAA | T | 12 | a0001c0001t0002g0266a0001c0013t0001g0090a0001c0013t0001g0138others(9): Show | 12 | HG01257.hp1 HG01496.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+292_1095+293d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996817 | ||||||
| chr19:16996838
|
A | G | 1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1095+273T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16996838 | ||||||
| chr19:16997003
|
G | T | 1 | a0002c0018t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1095+108C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16997003 | ||||||
| chr19:16997013
|
C | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1095+98G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16997013 | ||||||
| chr19:16997015
|
G | A | 94 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1095+96C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16997015 | ||||||
| chr19:16997058
|
G | A | 1 | a0029c0137t0002g0270 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1095+53C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16997058 | ||||||
| chr19:16997068
|
G | A | 3 | a0010c0004t0001g0243a0078c0086t0001g0242a0088c0047t0001g0161 | 3 | HG01257.hp1 HG01258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1095+43C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16997068 | ||||||
| chr19:16997084
|
G | A | 1 | a0008c0009t0001g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1095+27C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16997084 | ||||||
| chr19:16997100
|
C | T | 2 | a0005c0121t0002g0267a0027c0035t0001g0045 | 2 | HG01081.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1095+11G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 11/41 | chr19 | 16997100 | ||||||
| chr19:16997473
|
A | G | 65 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(62): Show | 65 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.868-135T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997473 | ||||||
| chr19:16997484
|
G | A | 2 | a0004c0005t0002g0211a0094c0060t0001g0262 | 2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.868-146C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997484 | ||||||
| chr19:16997625
|
C | T | 15 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(12): Show | 15 | HG00741.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.868-287G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997625 | ||||||
| chr19:16997626
|
G | A | 6 | a0005c0121t0002g0267a0008c0160t0001g0040a0027c0035t0001g0045others(3): Show | 6 | HG01081.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.868-288C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997626 | ||||||
| chr19:16997679
|
C | T | 15 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(12): Show | 15 | HG00741.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.868-341G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997679 | ||||||
| chr19:16997696
|
T | TA | 6 | a0005c0121t0002g0267a0008c0160t0001g0040a0027c0035t0001g0045others(3): Show | 6 | HG01081.hp2 HG02698.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.868-359dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997696 | ||||||
| chr19:16997712
|
C | T | 1 | a0032c0043t0001g0191 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.868-374G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997712 | ||||||
| chr19:16997713
|
G | A | 1 | a0004c0100t0002g0054 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.868-375C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997713 | ||||||
| chr19:16997784
|
A | G | 15 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(12): Show | 15 | HG00741.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.868-446T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997784 | ||||||
| chr19:16997877
|
C | T | 1 | a0006c0006t0001g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.868-539G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997877 | ||||||
| chr19:16997973
|
C | T | 1 | a0117c0110t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.868-635G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16997973 | ||||||
| chr19:16998036
|
G | A | 1 | a0115c0123t0001g0226 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.868-698C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998036 | ||||||
| chr19:16998059
|
G | C | 1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.868-721C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998059 | ||||||
| chr19:16998231
|
C | T | 1 | a0001c0102t0002g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.868-893G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998231 | ||||||
| chr19:16998471
|
T | A | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.868-1133A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998471 | ||||||
| chr19:16998540
|
T | C | 63 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(60): Show | 63 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.868-1202A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998540 | ||||||
| chr19:16998572
|
G | C | 1 | a0005c0003t0002g0244 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.868-1234C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998572 | ||||||
| chr19:16998593
|
G | A | 94 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.868-1255C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998593 | ||||||
| chr19:16998603
|
G | T | 6 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.868-1265C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998603 | ||||||
| chr19:16998615
|
G | A | 17 | a0003c0002t0002g0213a0009c0042t0001g0206a0016c0050t0001g0095others(14): Show | 17 | HG00741.hp2 HG02055.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.868-1277C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998615 | ||||||
| chr19:16998626
|
A | G | 220 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.868-1288T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998626 | ||||||
| chr19:16998738
|
A | G | 63 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(60): Show | 63 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.868-1400T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998738 | ||||||
| chr19:16998829
|
A | G | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.868-1491T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998829 | ||||||
| chr19:16998942
|
G | A | 15 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(12): Show | 15 | HG00741.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.867+1472C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16998942 | ||||||
| chr19:16999124
|
A | T | 4 | a0007c0052t0002g0119a0007c0053t0001g0156a0007c0119t0001g0122others(1): Show | 4 | HG02486.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+1290T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999124 | ||||||
| chr19:16999311
|
T | C | 4 | a0083c0112t0001g0096a0084c0111t0001g0097a0118c0139t0001g0108others(1): Show | 4 | HG00741.hp2 HG02683.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+1103A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999311 | ||||||
| chr19:16999318
|
C | T | 63 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(60): Show | 63 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.867+1096G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999318 | ||||||
| chr19:16999323
|
G | A | 2 | a0002c0058t0002g0149a0095c0057t0002g0134 | 2 | HG00140.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.867+1091C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999323 | ||||||
| chr19:16999347
|
G | A | 15 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(12): Show | 15 | HG00741.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.867+1067C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999347 | ||||||
| chr19:16999355
|
T | C | 220 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.867+1059A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999355 | ||||||
| chr19:16999356
|
G | A | 19 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(16): Show | 19 | HG00609.hp2 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.867+1058C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999356 | ||||||
| chr19:16999377
|
G | A | 2 | a0005c0121t0002g0267a0027c0035t0001g0045 | 2 | HG01081.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.867+1037C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999377 | ||||||
| chr19:16999394
|
T | C | 1 | a0117c0110t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.867+1020A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999394 | ||||||
| chr19:16999408
|
G | A | 1 | a0019c0146t0001g0198 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.867+1006C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999408 | ||||||
| chr19:16999462
|
A | G | 1 | a0114c0113t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.867+952T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999462 | ||||||
| chr19:16999516
|
C | T | 5 | a0040c0074t0002g0212a0040c0141t0002g0245a0041c0023t0002g0157others(2): Show | 5 | HG01099.hp1 HG01516.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.867+898G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999516 | ||||||
| chr19:16999585
|
C | A | 63 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(60): Show | 63 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.867+829G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999585 | ||||||
| chr19:16999585
|
C | CA | 52 | a0001c0001t0002g0219a0003c0002t0002g0092a0005c0003t0002g0051others(49): Show | 52 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.867+828dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999585 | ||||||
| chr19:16999596
|
A | AAG | 13 | a0016c0117t0001g0114a0016c0185t0001g0058a0028c0114t0001g0100others(10): Show | 13 | HG00741.hp2 HG02055.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.867+817_867+818ins others(2): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999596 | ||||||
| chr19:16999596
|
A | AG | 49 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(46): Show | 49 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.867+817_867+818ins others(1): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999596 | ||||||
| chr19:16999596
|
A | G | 1 | a0088c0047t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.867+818T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999596 | ||||||
| chr19:16999748
|
A | G | 45 | a0005c0003t0002g0051a0005c0003t0002g0125a0005c0003t0002g0167others(42): Show | 45 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.867+666T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999748 | ||||||
| chr19:16999762
|
C | T | 63 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(60): Show | 63 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.867+652G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999762 | ||||||
| chr19:16999772
|
C | A | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+642G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999772 | ||||||
| chr19:16999773
|
C | A | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+641G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999773 | ||||||
| chr19:16999774
|
A | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+640T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999774 | ||||||
| chr19:16999776
|
A | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+638T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999776 | ||||||
| chr19:16999783
|
G | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+631C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999783 | ||||||
| chr19:16999785
|
G | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+629C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999785 | ||||||
| chr19:16999786
|
C | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+628G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999786 | ||||||
| chr19:16999788
|
G | A | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+626C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999788 | ||||||
| chr19:16999789
|
G | A | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+625C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999789 | ||||||
| chr19:16999790
|
G | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+624C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999790 | ||||||
| chr19:16999792
|
C | A | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+622G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999792 | ||||||
| chr19:16999794
|
C | A | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+620G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999794 | ||||||
| chr19:16999795
|
C | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+619G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999795 | ||||||
| chr19:16999797
|
G | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+617C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999797 | ||||||
| chr19:16999798
|
G | A | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+616C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999798 | ||||||
| chr19:16999799
|
C | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+615G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999799 | ||||||
| chr19:16999801
|
A | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+613T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999801 | ||||||
| chr19:16999804
|
A | T | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+610T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999804 | ||||||
| chr19:16999810
|
G | A | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+604C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999810 | ||||||
| chr19:16999813
|
T | A | 1 | a0024c0030t0001g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.867+601A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999813 | ||||||
| chr19:16999884
|
G | A | 4 | a0083c0112t0001g0096a0084c0111t0001g0097a0118c0139t0001g0108others(1): Show | 4 | HG00741.hp2 HG02683.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+530C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999884 | ||||||
| chr19:16999922
|
C | A | 3 | a0007c0052t0002g0119a0007c0053t0001g0156a0099c0054t0001g0003 | 3 | HG02486.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.867+492G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999922 | ||||||
| chr19:16999924
|
C | T | 51 | a0005c0003t0002g0051a0005c0003t0002g0125a0005c0003t0002g0166others(48): Show | 51 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.867+490G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999924 | ||||||
| chr19:16999982
|
T | A | 1 | a0004c0100t0002g0054 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.867+432A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 16999982 | ||||||
| chr19:17000008
|
T | C | 2 | a0008c0009t0001g0247a0008c0150t0001g0273 | 2 | HG01071.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.867+406A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 17000008 | ||||||
| chr19:17000037
|
G | A | 2 | a0002c0120t0001g0074a0045c0118t0001g0024 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.867+377C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 17000037 | ||||||
| chr19:17000048
|
T | G | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.867+366A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 17000048 | ||||||
| chr19:17000080
|
T | A | 5 | a0016c0185t0001g0058a0028c0181t0002g0060a0028c0182t0001g0062others(2): Show | 5 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+334A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 17000080 | ||||||
| chr19:17000123
|
C | T | 1 | a0037c0093t0001g0274 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.867+291G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 17000123 | ||||||
| chr19:17000182
|
G | A | 1 | a0113c0136t0002g0169 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.867+232C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 17000182 | ||||||
| chr19:17000188
|
TCACACTT others(10): Show |
T | 63 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(60): Show | 63 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.867+209_867+225del others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 17000188 | ||||||
| chr19:17000234
|
G | T | 8 | a0008c0160t0001g0040a0021c0143t0001g0012a0055c0145t0001g0093others(5): Show | 8 | HG01884.hp2 HG02698.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.867+180C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 17000234 | ||||||
| chr19:17000387
|
G | A | 5 | a0016c0185t0001g0058a0028c0181t0002g0060a0028c0182t0001g0062others(2): Show | 5 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+27C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 17000387 | ||||||
| chr19:17000406
|
T | C | 2 | a0002c0120t0001g0074a0045c0118t0001g0024 | 2 | HG02922.hp2 NA19030.hp2 |
splice_region_variant&intron_variant | LOW | c.867+8A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 10/41 | chr19 | 17000406 | ||||||
| chr19:17000601
|
A | G | 209 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.759-79T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17000601 | ||||||
| chr19:17000713
|
C | T | 1 | a0118c0139t0001g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.759-191G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17000713 | ||||||
| chr19:17000750
|
G | T | 1 | a0002c0017t0001g0113 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.759-228C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17000750 | ||||||
| chr19:17000817
|
T | G | 1 | a0117c0110t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.759-295A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17000817 | ||||||
| chr19:17000864
|
T | C | 49 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(46): Show | 49 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.759-342A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17000864 | ||||||
| chr19:17000889
|
A | G | 64 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(61): Show | 64 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.759-367T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17000889 | ||||||
| chr19:17000891
|
C | T | 1 | a0118c0139t0001g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.759-369G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17000891 | ||||||
| chr19:17000927
|
G | A | 8 | a0008c0160t0001g0040a0021c0143t0001g0012a0055c0145t0001g0093others(5): Show | 8 | HG01884.hp2 HG02698.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.759-405C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17000927 | ||||||
| chr19:17001057
|
T | C | 44 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(41): Show | 44 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.759-535A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001057 | ||||||
| chr19:17001128
|
C | A | 65 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(62): Show | 65 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.759-606G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001128 | ||||||
| chr19:17001250
|
T | G | 211 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.759-728A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001250 | ||||||
| chr19:17001293
|
CCTGGGCG others(13): Show |
C | 2 | a0034c0070t0002g0091a0056c0072t0001g0094 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.759-791_759-772del others(20): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001293 | ||||||
| chr19:17001299
|
C | G | 65 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(62): Show | 65 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.759-777G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001299 | ||||||
| chr19:17001316
|
G | A | 1 | a0033c0040t0001g0265 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.759-794C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001316 | ||||||
| chr19:17001320
|
G | GA | 14 | a0002c0120t0001g0074a0008c0009t0001g0231a0009c0010t0002g0078others(11): Show | 14 | HG00423.hp2 HG01978.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.759-799dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001320 | ||||||
| chr19:17001320
|
GA | G | 166 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.759-799delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001320 | ||||||
| chr19:17001320
|
GAA | G | 8 | a0004c0014t0002g0038a0005c0003t0002g0166a0015c0008t0001g0005others(5): Show | 8 | HG01361.hp2 HG01515.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.759-800_759-799del others(2): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001320 | ||||||
| chr19:17001457
|
G | GGAGAGGA others(29): Show |
61 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(58): Show | 61 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.758+808_758+809ins others(36): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001457 | ||||||
| chr19:17001470
|
C | CT | 41 | a0005c0003t0002g0051a0005c0003t0002g0125a0005c0003t0002g0166others(38): Show | 41 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.758+795dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001470 | ||||||
| chr19:17001474
|
G | A | 6 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.758+792C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001474 | ||||||
| chr19:17001492
|
G | A | 61 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(58): Show | 61 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.758+774C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001492 | ||||||
| chr19:17001554
|
T | C | 61 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(58): Show | 61 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.758+712A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001554 | ||||||
| chr19:17001591
|
G | A | 60 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(57): Show | 60 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.758+675C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001591 | ||||||
| chr19:17001593
|
C | T | 60 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(57): Show | 60 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.758+673G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001593 | ||||||
| chr19:17001605
|
G | T | 1 | a0001c0001t0002g0277 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.758+661C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001605 | ||||||
| chr19:17001768
|
C | A | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.758+498G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001768 | ||||||
| chr19:17001808
|
G | A | 1 | a0005c0121t0002g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.758+458C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001808 | ||||||
| chr19:17001837
|
A | G | 62 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(59): Show | 62 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.758+429T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001837 | ||||||
| chr19:17001856
|
G | A | 15 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(12): Show | 15 | HG01884.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.758+410C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001856 | ||||||
| chr19:17001901
|
C | G | 1 | a0011c0012t0002g0202 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.758+365G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001901 | ||||||
| chr19:17001908
|
C | G | 45 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(42): Show | 45 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.758+358G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001908 | ||||||
| chr19:17001967
|
GAGGGAGG others(10): Show |
G | 1 | a0004c0180t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.758+282_758+298del others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001967 | ||||||
| chr19:17001975
|
A | G | 85 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(82): Show | 85 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.758+291T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001975 | ||||||
| chr19:17001979
|
C | A | 1 | a0008c0009t0001g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.758+287G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17001979 | ||||||
| chr19:17002017
|
T | C | 61 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(58): Show | 61 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.758+249A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17002017 | ||||||
| chr19:17002064
|
C | T | 70 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(67): Show | 70 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.758+202G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17002064 | ||||||
| chr19:17002071
|
T | A | 70 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(67): Show | 70 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.758+195A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17002071 | ||||||
| chr19:17002111
|
C | T | 68 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(65): Show | 68 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.758+155G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17002111 | ||||||
| chr19:17002191
|
C | A | 59 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(56): Show | 59 | HG00140.hp2 HG00642.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.758+75G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17002191 | ||||||
| chr19:17002205
|
C | T | 6 | a0047c0046t0002g0135a0047c0046t0002g0136a0061c0142t0002g0015others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.758+61G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17002205 | ||||||
| chr19:17002230
|
C | T | 1 | a0022c0032t0001g0228 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.758+36G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 9/41 | chr19 | 17002230 | ||||||
| chr19:17002572
|
T | TC | 68 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(65): Show | 68 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.674-223dupG | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002572 | ||||||
| chr19:17002657
|
T | C | 68 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(65): Show | 68 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.674-307A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002657 | ||||||
| chr19:17002719
|
G | C | 106 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0102t0002g0079others(103): Show | 106 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.674-369C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002719 | ||||||
| chr19:17002739
|
G | C | 1 | a0005c0131t0002g0063 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.674-389C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002739 | ||||||
| chr19:17002751
|
T | G | 7 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.674-401A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002751 | ||||||
| chr19:17002817
|
A | G | 47 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0102t0002g0079others(44): Show | 47 | HG00423.hp2 HG00597.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.674-467T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002817 | ||||||
| chr19:17002824
|
G | A | 106 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0102t0002g0079others(103): Show | 106 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.674-474C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002824 | ||||||
| chr19:17002902
|
TTTC | T | 4 | a0020c0011t0001g0017a0020c0011t0001g0020a0020c0011t0001g0021others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-555_674-553del others(3): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002902 | ||||||
| chr19:17002905
|
C | CT | 11 | a0001c0001t0002g0199a0001c0033t0002g0002a0001c0033t0002g0027others(8): Show | 11 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-556dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002905 | ||||||
| chr19:17002905
|
C | CTT | 89 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0102t0002g0079others(86): Show | 89 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.674-557_674-556dup others(2): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002905 | ||||||
| chr19:17002905
|
C | CTTT | 7 | a0006c0006t0001g0220a0007c0016t0001g0123a0007c0016t0001g0124others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.674-558_674-556dup others(3): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002905 | ||||||
| chr19:17002909
|
TC | T | 13 | a0016c0050t0001g0095a0016c0116t0001g0010a0016c0117t0001g0114others(10): Show | 13 | HG01167.hp2 HG01361.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.674-560delG | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002909 | ||||||
| chr19:17002910
|
C | T | 207 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.674-560G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17002910 | ||||||
| chr19:17003092
|
G | C | 1 | a0004c0100t0002g0054 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.674-742C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003092 | ||||||
| chr19:17003142
|
A | G | 1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.674-792T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003142 | ||||||
| chr19:17003180
|
G | C | 1 | a0002c0120t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.674-830C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003180 | ||||||
| chr19:17003193
|
A | G | 98 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0102t0002g0079others(95): Show | 98 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.674-843T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003193 | ||||||
| chr19:17003335
|
G | A | 50 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(47): Show | 50 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.673+938C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003335 | ||||||
| chr19:17003404
|
T | C | 10 | a0001c0013t0001g0138a0021c0143t0001g0012a0023c0075t0001g0137others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.673+869A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003404 | ||||||
| chr19:17003551
|
C | T | 2 | a0049c0154t0001g0195a0060c0157t0002g0142 | 2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.673+722G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003551 | ||||||
| chr19:17003778
|
C | CA | 10 | a0004c0100t0002g0054a0006c0006t0001g0220a0010c0004t0001g0089others(7): Show | 10 | HG01261.hp1 HG01928.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.673+494dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003778 | ||||||
| chr19:17003795
|
T | C | 223 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.673+478A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003795 | ||||||
| chr19:17003827
|
C | T | 1 | a0008c0009t0001g0247 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.673+446G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003827 | ||||||
| chr19:17003852
|
C | T | 16 | a0007c0119t0001g0122a0016c0050t0001g0095a0016c0116t0001g0010others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.673+421G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003852 | ||||||
| chr19:17003872
|
C | T | 82 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(79): Show | 82 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.673+401G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003872 | ||||||
| chr19:17003895
|
C | A | 5 | a0001c0001t0002g0199a0001c0033t0002g0002a0001c0033t0002g0027others(2): Show | 5 | HG00099.hp2 HG00741.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+378G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003895 | ||||||
| chr19:17003913
|
C | CT | 6 | a0001c0001t0002g0199a0001c0033t0002g0002a0001c0033t0002g0027others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.673+359dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003913 | ||||||
| chr19:17003913
|
C | CTT | 10 | a0001c0013t0001g0138a0021c0143t0001g0012a0023c0075t0001g0137others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.673+358_673+359dup others(2): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17003913 | ||||||
| chr19:17004075
|
T | C | 50 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(47): Show | 50 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.673+198A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17004075 | ||||||
| chr19:17004165
|
G | A | 1 | a0005c0121t0002g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.673+108C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 8/41 | chr19 | 17004165 | ||||||
| chr19:17004439
|
G | A | 1 | a0016c0116t0001g0010 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.560-53C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17004439 | ||||||
| chr19:17004772
|
T | C | 51 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(48): Show | 51 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.560-386A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17004772 | ||||||
| chr19:17004822
|
T | C | 1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.560-436A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17004822 | ||||||
| chr19:17004879
|
A | G | 2 | a0049c0154t0001g0195a0060c0157t0002g0142 | 2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.560-493T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17004879 | ||||||
| chr19:17004894
|
T | C | 50 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(47): Show | 50 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.560-508A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17004894 | ||||||
| chr19:17004896
|
C | T | 51 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(48): Show | 51 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.560-510G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17004896 | ||||||
| chr19:17004907
|
G | T | 1 | a0019c0039t0001g0238 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.560-521C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17004907 | ||||||
| chr19:17004912
|
T | C | 50 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(47): Show | 50 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.560-526A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17004912 | ||||||
| chr19:17004964
|
C | G | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.560-578G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17004964 | ||||||
| chr19:17005037
|
A | G | 39 | a0001c0013t0001g0090a0001c0102t0002g0079a0004c0005t0002g0188others(36): Show | 39 | HG00423.hp2 HG00597.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.560-651T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005037 | ||||||
| chr19:17005088
|
A | G | 213 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.560-702T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005088 | ||||||
| chr19:17005089
|
A | C | 213 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.560-703T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005089 | ||||||
| chr19:17005095
|
G | A | 1 | a0068c0095t0002g0064 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.560-709C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005095 | ||||||
| chr19:17005110
|
A | G | 2 | a0047c0046t0002g0135a0047c0046t0002g0136 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-724T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005110 | ||||||
| chr19:17005262
|
C | T | 1 | a0038c0109t0002g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.560-876G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005262 | ||||||
| chr19:17005291
|
G | T | 1 | a0009c0010t0002g0078 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.560-905C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005291 | ||||||
| chr19:17005361
|
G | T | 1 | a0116c0138t0001g0028 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.560-975C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005361 | ||||||
| chr19:17005426
|
C | T | 11 | a0002c0120t0001g0074a0005c0003t0002g0125a0006c0006t0001g0131others(8): Show | 11 | HG00140.hp1 HG01167.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.560-1040G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005426 | ||||||
| chr19:17005435
|
T | C | 99 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.560-1049A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005435 | ||||||
| chr19:17005516
|
G | A | 3 | a0001c0001t0002g0147a0024c0030t0001g0148a0024c0030t0001g0173 | 3 | NA18947.hp2 NA19011.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.560-1130C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005516 | ||||||
| chr19:17005668
|
T | C | 1 | a0041c0023t0002g0258 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.560-1282A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005668 | ||||||
| chr19:17005711
|
C | T | 6 | a0001c0007t0002g0246a0004c0005t0002g0046a0004c0100t0002g0054others(3): Show | 6 | HG01192.hp1 HG01361.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.560-1325G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005711 | ||||||
| chr19:17005785
|
T | C | 91 | a0001c0013t0001g0090a0001c0102t0002g0079a0002c0017t0001g0112others(88): Show | 91 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.560-1399A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005785 | ||||||
| chr19:17005964
|
G | GT | 101 | a0001c0013t0001g0090a0001c0102t0002g0079a0002c0017t0001g0112others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.560-1579dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17005964 | ||||||
| chr19:17006045
|
C | A | 1 | a0015c0008t0001g0174 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.560-1659G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006045 | ||||||
| chr19:17006108
|
A | G | 221 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.560-1722T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006108 | ||||||
| chr19:17006228
|
C | G | 6 | a0001c0001t0002g0199a0001c0033t0002g0002a0001c0033t0002g0027others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-1842G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006228 | ||||||
| chr19:17006276
|
T | C | 2 | a0086c0179t0001g0102a0087c0178t0001g0103 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.560-1890A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006276 | ||||||
| chr19:17006298
|
C | T | 1 | a0008c0009t0001g0247 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.560-1912G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006298 | ||||||
| chr19:17006394
|
G | A | 6 | a0003c0045t0002g0218a0006c0006t0001g0086a0008c0009t0001g0217others(3): Show | 6 | HG01081.hp1 HG01257.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.560-2008C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006394 | ||||||
| chr19:17006531
|
G | GA | 10 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0018t0001g0099others(7): Show | 10 | HG02027.hp1 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.559+1973dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006531 | ||||||
| chr19:17006531
|
GA | G | 54 | a0001c0013t0001g0090a0001c0102t0002g0079a0002c0120t0001g0074others(51): Show | 54 | HG00140.hp1 HG00423.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.559+1973delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006531 | ||||||
| chr19:17006565
|
A | G | 12 | a0002c0120t0001g0074a0005c0003t0002g0125a0006c0006t0001g0131others(9): Show | 12 | HG00140.hp1 HG01167.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.559+1940T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006565 | ||||||
| chr19:17006627
|
C | G | 15 | a0007c0119t0001g0122a0016c0050t0001g0095a0016c0116t0001g0010others(12): Show | 15 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.559+1878G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006627 | ||||||
| chr19:17006752
|
T | C | 2 | a0005c0121t0002g0267a0027c0035t0001g0045 | 2 | HG01081.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.559+1753A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006752 | ||||||
| chr19:17006827
|
G | T | 1 | a0002c0017t0001g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.559+1678C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006827 | ||||||
| chr19:17006946
|
A | G | 3 | a0026c0034t0002g0032a0026c0034t0002g0033a0046c0036t0001g0031 | 3 | NA18965.hp1 NA19065.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.559+1559T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006946 | ||||||
| chr19:17006954
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.559+1551G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006954 | ||||||
| chr19:17006973
|
T | C | 6 | a0001c0001t0002g0199a0001c0033t0002g0002a0001c0033t0002g0027others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+1532A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006973 | ||||||
| chr19:17006984
|
C | T | 6 | a0004c0014t0002g0222a0004c0014t0002g0223a0011c0012t0002g0210others(3): Show | 6 | HG00423.hp2 HG00597.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.559+1521G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17006984 | ||||||
| chr19:17007060
|
C | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.559+1445G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007060 | ||||||
| chr19:17007147
|
A | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.559+1358T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007147 | ||||||
| chr19:17007250
|
C | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.559+1255G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007250 | ||||||
| chr19:17007334
|
T | A | 40 | a0001c0013t0001g0090a0001c0102t0002g0079a0004c0014t0002g0038others(37): Show | 40 | HG00423.hp2 HG00597.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.559+1171A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007334 | ||||||
| chr19:17007411
|
A | C | 1 | a0013c0049t0002g0170 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.559+1094T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007411 | ||||||
| chr19:17007465
|
A | G | 1 | a0005c0003t0002g0125 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.559+1040T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007465 | ||||||
| chr19:17007601
|
C | T | 31 | a0001c0013t0001g0090a0001c0102t0002g0079a0004c0014t0002g0038others(28): Show | 31 | HG00423.hp2 HG00597.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.559+904G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007601 | ||||||
| chr19:17007623
|
C | T | 46 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(43): Show | 46 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.559+882G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007623 | ||||||
| chr19:17007628
|
A | AC | 4 | a0002c0019t0001g0139a0019c0039t0001g0227a0020c0011t0001g0021others(1): Show | 4 | HG01978.hp1 HG02055.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+876dupG | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007628 | ||||||
| chr19:17007772
|
T | C | 2 | a0005c0121t0002g0267a0027c0035t0001g0045 | 2 | HG01081.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.559+733A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007772 | ||||||
| chr19:17007838
|
A | G | 4 | a0083c0112t0001g0096a0084c0111t0001g0097a0118c0139t0001g0108others(1): Show | 4 | HG00741.hp2 HG02683.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+667T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007838 | ||||||
| chr19:17007869
|
G | T | 3 | a0004c0005t0002g0188a0004c0005t0002g0211a0106c0134t0001g0109 | 3 | HG03669.hp1 NA18959.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.559+636C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007869 | ||||||
| chr19:17007890
|
G | A | 1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.559+615C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007890 | ||||||
| chr19:17007919
|
C | A | 41 | a0001c0013t0001g0090a0001c0102t0002g0079a0004c0014t0002g0038others(38): Show | 41 | HG00423.hp2 HG00597.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.559+586G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17007919 | ||||||
| chr19:17008001
|
T | C | 47 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(44): Show | 47 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.559+504A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17008001 | ||||||
| chr19:17008029
|
C | T | 1 | a0104c0133t0002g0241 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.559+476G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17008029 | ||||||
| chr19:17008033
|
G | C | 2 | a0003c0002t0002g0105a0003c0002t0002g0200 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.559+472C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17008033 | ||||||
| chr19:17008082
|
G | A | 1 | a0016c0050t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.559+423C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17008082 | ||||||
| chr19:17008093
|
C | T | 1 | a0039c0107t0001g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.559+412G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17008093 | ||||||
| chr19:17008124
|
G | A | 1 | a0065c0101t0001g0001 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.559+381C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17008124 | ||||||
| chr19:17008212
|
C | T | 2 | a0008c0160t0001g0040a0039c0076t0001g0126 | 2 | HG01975.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.559+293G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17008212 | ||||||
| chr19:17008266
|
C | T | 82 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(79): Show | 82 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.559+239G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17008266 | ||||||
| chr19:17008406
|
TG | T | 6 | a0001c0007t0002g0246a0003c0002t0002g0039a0004c0005t0002g0046others(3): Show | 6 | HG01192.hp1 HG01361.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.559+98delC | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 7/41 | chr19 | 17008406 | ||||||
| chr19:17008750
|
T | C | 273 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.505-191A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17008750 | ||||||
| chr19:17008759
|
C | A | 1 | a0004c0014t0002g0038 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.505-200G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17008759 | ||||||
| chr19:17008791
|
C | A | 10 | a0002c0120t0001g0074a0004c0180t0001g0041a0010c0004t0001g0068others(7): Show | 10 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.505-232G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17008791 | ||||||
| chr19:17008935
|
T | C | 46 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(43): Show | 46 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.504+368A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17008935 | ||||||
| chr19:17008968
|
C | T | 78 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(75): Show | 78 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.504+335G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17008968 | ||||||
| chr19:17008970
|
C | A | 1 | a0055c0145t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.504+333G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17008970 | ||||||
| chr19:17009095
|
TC | T | 11 | a0001c0013t0001g0138a0023c0075t0001g0137a0034c0070t0002g0091others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.504+207delG | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17009095 | ||||||
| chr19:17009096
|
CA | C | 140 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.504+206delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17009096 | ||||||
| chr19:17009113
|
C | T | 11 | a0001c0013t0001g0138a0023c0075t0001g0137a0034c0070t0002g0091others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.504+190G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17009113 | ||||||
| chr19:17009124
|
A | G | 8 | a0001c0001t0002g0199a0001c0033t0002g0002a0001c0033t0002g0027others(5): Show | 8 | HG00099.hp2 HG00741.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+179T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17009124 | ||||||
| chr19:17009145
|
G | A | 11 | a0001c0013t0001g0138a0023c0075t0001g0137a0034c0070t0002g0091others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.504+158C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17009145 | ||||||
| chr19:17009280
|
G | A | 1 | a0008c0160t0001g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.504+23C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 6/41 | chr19 | 17009280 | ||||||
| chr19:17009492
|
G | A | 7 | a0001c0013t0001g0090a0072c0081t0001g0067a0083c0112t0001g0096others(4): Show | 7 | HG00741.hp2 HG01891.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-172C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009492 | ||||||
| chr19:17009546
|
G | A | 2 | a0016c0185t0001g0058a0028c0182t0001g0062 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.487-226C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009546 | ||||||
| chr19:17009557
|
G | A | 6 | a0004c0180t0001g0041a0016c0185t0001g0058a0028c0181t0002g0060others(3): Show | 6 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-237C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009557 | ||||||
| chr19:17009557
|
G | T | 1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.487-237C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009557 | ||||||
| chr19:17009601
|
C | T | 6 | a0004c0180t0001g0041a0016c0185t0001g0058a0028c0181t0002g0060others(3): Show | 6 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-281G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009601 | ||||||
| chr19:17009609
|
C | T | 11 | a0001c0013t0001g0138a0023c0075t0001g0137a0034c0070t0002g0091others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.487-289G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009609 | ||||||
| chr19:17009663
|
A | C | 4 | a0002c0120t0001g0074a0010c0004t0001g0068a0069c0098t0001g0065others(1): Show | 4 | HG02976.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-343T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009663 | ||||||
| chr19:17009667
|
G | A | 8 | a0005c0003t0002g0125a0006c0006t0001g0131a0006c0015t0002g0133others(5): Show | 8 | HG00140.hp1 HG01167.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-347C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009667 | ||||||
| chr19:17009699
|
A | G | 66 | a0001c0013t0001g0090a0002c0017t0001g0112a0002c0017t0001g0113others(63): Show | 66 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.487-379T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009699 | ||||||
| chr19:17009721
|
C | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.487-401G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009721 | ||||||
| chr19:17009722
|
G | A | 64 | a0001c0013t0001g0090a0002c0017t0001g0112a0002c0017t0001g0113others(61): Show | 64 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.487-402C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009722 | ||||||
| chr19:17009773
|
C | CA | 14 | a0001c0013t0001g0138a0015c0008t0001g0174a0023c0075t0001g0137others(11): Show | 14 | HG01109.hp1 HG01516.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.487-454dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009773 | ||||||
| chr19:17009773
|
CA | C | 11 | a0001c0001t0002g0048a0001c0013t0001g0090a0004c0180t0001g0041others(8): Show | 11 | HG00741.hp2 HG01891.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.487-454delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009773 | ||||||
| chr19:17009890
|
G | A | 1 | a0001c0033t0002g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.487-570C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009890 | ||||||
| chr19:17009925
|
C | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.487-605G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009925 | ||||||
| chr19:17009997
|
C | A | 3 | a0002c0019t0001g0008a0002c0019t0001g0139a0088c0047t0001g0161 | 3 | HG02622.hp1 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.487-677G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17009997 | ||||||
| chr19:17010173
|
T | C | 7 | a0001c0013t0001g0090a0072c0081t0001g0067a0083c0112t0001g0096others(4): Show | 7 | HG00741.hp2 HG01891.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-853A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17010173 | ||||||
| chr19:17010223
|
C | CT | 10 | a0002c0120t0001g0074a0004c0180t0001g0041a0010c0004t0001g0068others(7): Show | 10 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.487-904dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17010223 | ||||||
| chr19:17010693
|
T | C | 2 | a0035c0026t0001g0233a0035c0026t0001g0234 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.486+771A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17010693 | ||||||
| chr19:17010714
|
A | C | 1 | a0006c0015t0002g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.486+750T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17010714 | ||||||
| chr19:17010723
|
A | C | 58 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(55): Show | 58 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.486+741T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17010723 | ||||||
| chr19:17010749
|
G | C | 5 | a0001c0001t0002g0199a0001c0033t0002g0002a0001c0033t0002g0027others(2): Show | 5 | HG00099.hp2 HG00741.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+715C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17010749 | ||||||
| chr19:17010838
|
C | A | 7 | a0001c0013t0001g0090a0072c0081t0001g0067a0083c0112t0001g0096others(4): Show | 7 | HG00741.hp2 HG01891.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+626G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17010838 | ||||||
| chr19:17010938
|
G | A | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.486+526C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17010938 | ||||||
| chr19:17011035
|
G | GA | 17 | a0005c0003t0002g0244a0016c0050t0001g0095a0016c0116t0001g0010others(14): Show | 17 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.486+428dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17011035 | ||||||
| chr19:17011036
|
A | G | 1 | a0040c0141t0002g0245 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.486+428T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17011036 | ||||||
| chr19:17011134
|
G | A | 41 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0017t0001g0162others(38): Show | 41 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.486+330C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17011134 | ||||||
| chr19:17011199
|
G | A | 11 | a0001c0013t0001g0138a0023c0075t0001g0137a0034c0070t0002g0091others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.486+265C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17011199 | ||||||
| chr19:17011201
|
A | G | 1 | a0044c0021t0002g0269 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.486+263T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17011201 | ||||||
| chr19:17011222
|
A | C | 29 | a0001c0102t0002g0079a0002c0059t0001g0044a0002c0062t0002g0176others(26): Show | 29 | HG00423.hp2 HG00597.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.486+242T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17011222 | ||||||
| chr19:17011297
|
C | T | 1 | a0012c0028t0002g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.486+167G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 5/41 | chr19 | 17011297 | ||||||
| chr19:17011820
|
G | A | 119 | a0001c0001t0002g0048a0001c0007t0002g0053a0002c0017t0001g0112others(116): Show | 119 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.268-63C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17011820 | ||||||
| chr19:17011838
|
G | A | 22 | a0002c0018t0001g0099a0004c0180t0001g0041a0008c0160t0001g0040others(19): Show | 22 | HG00735.hp2 HG00741.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.268-81C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17011838 | ||||||
| chr19:17012023
|
A | T | 1 | a0011c0012t0002g0202 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.268-266T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012023 | ||||||
| chr19:17012073
|
GT | G | 6 | a0002c0017t0001g0162a0028c0181t0002g0060a0042c0174t0001g0160others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-317delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012073 | ||||||
| chr19:17012194
|
T | C | 9 | a0001c0102t0002g0079a0002c0059t0001g0044a0002c0062t0002g0176others(6): Show | 9 | HG00423.hp2 HG00597.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.268-437A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012194 | ||||||
| chr19:17012310
|
C | T | 1 | a0107c0122t0001g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.268-553G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012310 | ||||||
| chr19:17012326
|
TTTTC | T | 8 | a0001c0001t0002g0219a0001c0007t0002g0053a0001c0033t0002g0002others(5): Show | 8 | HG00597.hp1 HG00741.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.268-573_268-570del others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012326 | ||||||
| chr19:17012343
|
TTTC | T | 67 | a0002c0058t0002g0149a0003c0002t0002g0092a0003c0002t0002g0196others(64): Show | 67 | HG00140.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.268-589_268-587del others(3): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012343 | ||||||
| chr19:17012346
|
C | CT | 18 | a0001c0001t0002g0276a0001c0033t0002g0027a0002c0056t0001g0081others(15): Show | 18 | HG00099.hp2 HG00735.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.268-590dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012346 | ||||||
| chr19:17012350
|
C | CT | 23 | a0001c0013t0001g0090a0002c0018t0001g0099a0002c0176t0001g0014others(20): Show | 23 | HG00642.hp1 HG01109.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.268-594dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012350 | ||||||
| chr19:17012350
|
C | T | 84 | a0001c0001t0002g0219a0001c0007t0002g0053a0001c0013t0001g0138others(81): Show | 84 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.268-593G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012350 | ||||||
| chr19:17012427
|
G | A | 1 | a0118c0139t0001g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.268-670C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012427 | ||||||
| chr19:17012428
|
G | A | 1 | a0117c0110t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.268-671C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012428 | ||||||
| chr19:17012487
|
A | G | 1 | a0024c0092t0001g0260 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.268-730T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012487 | ||||||
| chr19:17012662
|
G | C | 1 | a0095c0057t0002g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.268-905C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012662 | ||||||
| chr19:17012773
|
C | G | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.268-1016G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012773 | ||||||
| chr19:17012774
|
C | A | 1 | a0045c0118t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.268-1017G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012774 | ||||||
| chr19:17012874
|
T | C | 13 | a0001c0001t0002g0147a0001c0001t0002g0199a0003c0151t0001g0143others(10): Show | 13 | HG00642.hp1 HG01346.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.268-1117A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012874 | ||||||
| chr19:17012907
|
C | T | 2 | a0005c0121t0002g0267a0027c0035t0001g0045 | 2 | HG01081.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.268-1150G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17012907 | ||||||
| chr19:17013040
|
C | G | 237 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.268-1283G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013040 | ||||||
| chr19:17013070
|
A | G | 2 | a0074c0080t0001g0082a0081c0079t0001g0080 | 2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.268-1313T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013070 | ||||||
| chr19:17013234
|
C | A | 1 | a0036c0025t0002g0189 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.268-1477G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013234 | ||||||
| chr19:17013252
|
T | C | 6 | a0002c0017t0001g0162a0042c0174t0001g0160a0088c0047t0001g0161others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-1495A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013252 | ||||||
| chr19:17013322
|
A | G | 169 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.268-1565T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013322 | ||||||
| chr19:17013330
|
G | A | 5 | a0010c0004t0001g0068a0057c0073t0001g0066a0069c0098t0001g0065others(2): Show | 5 | HG02615.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.268-1573C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013330 | ||||||
| chr19:17013451
|
C | A | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-1694G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013451 | ||||||
| chr19:17013452
|
C | G | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-1695G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013452 | ||||||
| chr19:17013453
|
A | G | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-1696T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013453 | ||||||
| chr19:17013497
|
C | A | 1 | a0017c0147t0001g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.268-1740G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013497 | ||||||
| chr19:17013512
|
A | AAAAAT | 22 | a0001c0033t0002g0027a0002c0120t0001g0074a0005c0003t0002g0125others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(19): Show |
intron_variant | MODIFIER | c.268-1760_268-1756d others(7): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013512 | ||||||
| chr19:17013512
|
A | AAAAATAA others(3): Show |
65 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0199others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.268-1765_268-1756d others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013512 | ||||||
| chr19:17013512
|
A | AAAAATAA others(8): Show |
19 | a0002c0017t0001g0162a0014c0105t0001g0140a0016c0185t0001g0058others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.268-1770_268-1756d others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013512 | ||||||
| chr19:17013512
|
A | AAAAATAA others(13): Show |
7 | a0015c0008t0001g0005a0028c0114t0001g0100a0045c0118t0001g0024others(4): Show | 7 | HG01515.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.268-1775_268-1756d others(22): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013512 | ||||||
| chr19:17013512
|
A | AAAAATAA others(18): Show |
101 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(98): Show | 101 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.268-1780_268-1756d others(27): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013512 | ||||||
| chr19:17013512
|
A | AAAAATAA others(23): Show |
29 | a0001c0001t0002g0185a0002c0019t0001g0139a0002c0058t0002g0149others(26): Show | 29 | HG00609.hp2 HG01168.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.268-1785_268-1756d others(32): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013512 | ||||||
| chr19:17013512
|
A | AAAAATAA others(28): Show |
5 | a0007c0052t0002g0119a0008c0160t0001g0040a0016c0050t0001g0095others(2): Show | 5 | HG01928.hp2 HG02559.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-1756_268-1755i others(37): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013512 | ||||||
| chr19:17013512
|
A | AAAAATAA others(33): Show |
5 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0018t0001g0115others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.268-1756_268-1755i others(42): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013512 | ||||||
| chr19:17013562
|
T | C | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-1805A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013562 | ||||||
| chr19:17013563
|
A | AGT | 10 | a0002c0017t0001g0112a0002c0017t0001g0113a0002c0018t0001g0115others(7): Show | 10 | HG01928.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.268-1808_268-1807d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013563 | ||||||
| chr19:17013640
|
G | C | 4 | a0015c0008t0001g0005a0017c0147t0001g0009a0029c0067t0001g0004others(1): Show | 4 | HG01515.hp1 HG03209.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-1883C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013640 | ||||||
| chr19:17013691
|
T | C | 5 | a0010c0004t0001g0068a0057c0073t0001g0066a0069c0098t0001g0065others(2): Show | 5 | HG02615.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.268-1934A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013691 | ||||||
| chr19:17013771
|
A | G | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-2014T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013771 | ||||||
| chr19:17013777
|
T | C | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-2020A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013777 | ||||||
| chr19:17013800
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.268-2043C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013800 | ||||||
| chr19:17013881
|
A | G | 79 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0199others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.268-2124T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013881 | ||||||
| chr19:17013884
|
ATTCC | A | 142 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(139): Show | 142 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.268-2131_268-2128d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013884 | ||||||
| chr19:17013889
|
T | C | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-2132A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013889 | ||||||
| chr19:17013919
|
C | CCTCCCTC others(5): Show |
1 | a0002c0019t0001g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268-2174_268-2163d others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013919 | ||||||
| chr19:17013940
|
C | T | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-2183G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013940 | ||||||
| chr19:17013965
|
T | G | 72 | a0001c0013t0001g0090a0001c0013t0001g0138a0001c0033t0002g0027others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.268-2208A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013965 | ||||||
| chr19:17013983
|
CCTA | C | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-2229_268-2227d others(5): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17013983 | ||||||
| chr19:17014000
|
T | TTCCC | 63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-2247_268-2244d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014000 | ||||||
| chr19:17014016
|
C | A | 40 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0018t0001g0099others(37): Show | 40 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.268-2259G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014016 | ||||||
| chr19:17014020
|
A | T | 40 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0018t0001g0099others(37): Show | 40 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.268-2263T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014020 | ||||||
| chr19:17014024
|
C | T | 111 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0199others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.268-2267G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014024 | ||||||
| chr19:17014026
|
C | T | 40 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0018t0001g0099others(37): Show | 40 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.268-2269G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014026 | ||||||
| chr19:17014028
|
C | T | 40 | a0001c0013t0001g0090a0001c0013t0001g0138a0002c0018t0001g0099others(37): Show | 40 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.268-2271G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014028 | ||||||
| chr19:17014041
|
T | C | 103 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(100): Show | 103 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.268-2284A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014041 | ||||||
| chr19:17014041
|
T | TTCTC | 111 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0199others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.268-2288_268-2285d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014041 | ||||||
| chr19:17014043
|
C | CTCTCTCT others(3): Show |
63 | a0001c0001t0002g0048a0001c0001t0002g0219a0001c0007t0002g0053others(60): Show | 63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.268-2287_268-2286i others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014043 | ||||||
| chr19:17014215
|
C | T | 2 | a0010c0004t0001g0243a0078c0086t0001g0242 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.268-2458G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014215 | ||||||
| chr19:17014367
|
A | AT | 69 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0199others(66): Show | 69 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.268-2611dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014367 | ||||||
| chr19:17014410
|
C | A | 1 | a0002c0019t0001g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268-2653G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014410 | ||||||
| chr19:17014466
|
A | T | 4 | a0004c0014t0002g0038a0008c0009t0001g0197a0019c0146t0001g0198others(1): Show | 4 | HG00609.hp1 HG02015.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-2709T>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014466 | ||||||
| chr19:17014875
|
C | G | 5 | a0010c0004t0001g0068a0057c0073t0001g0066a0069c0098t0001g0065others(2): Show | 5 | HG02615.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.268-3118G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014875 | ||||||
| chr19:17014972
|
T | G | 1 | a0003c0002t0002g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.268-3215A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17014972 | ||||||
| chr19:17015115
|
G | A | 12 | a0005c0003t0002g0125a0006c0006t0001g0131a0006c0015t0002g0133others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.268-3358C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015115 | ||||||
| chr19:17015129
|
C | T | 1 | a0042c0174t0001g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.268-3372G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015129 | ||||||
| chr19:17015265
|
G | T | 11 | a0002c0017t0001g0162a0010c0004t0001g0068a0042c0174t0001g0160others(8): Show | 11 | HG02109.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.268-3508C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015265 | ||||||
| chr19:17015433
|
G | T | 10 | a0002c0176t0001g0014a0007c0119t0001g0122a0016c0116t0001g0010others(7): Show | 10 | HG01361.hp1 HG01884.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.268-3676C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015433 | ||||||
| chr19:17015456
|
T | C | 62 | a0001c0007t0002g0036a0001c0102t0002g0079a0002c0017t0001g0162others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.268-3699A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015456 | ||||||
| chr19:17015461
|
C | G | 2 | a0002c0019t0001g0139a0007c0053t0001g0156 | 2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.268-3704G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015461 | ||||||
| chr19:17015462
|
C | T | 2 | a0007c0016t0001g0123a0007c0016t0001g0124 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.268-3705G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015462 | ||||||
| chr19:17015573
|
C | G | 76 | a0001c0007t0002g0036a0001c0013t0001g0090a0001c0013t0001g0138others(73): Show | 76 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.268-3816G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015573 | ||||||
| chr19:17015779
|
C | T | 164 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0007t0002g0036others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.268-4022G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015779 | ||||||
| chr19:17015807
|
G | C | 12 | a0002c0017t0001g0162a0002c0019t0001g0008a0010c0004t0001g0068others(9): Show | 12 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.268-4050C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015807 | ||||||
| chr19:17015837
|
G | T | 6 | a0002c0056t0001g0081a0045c0051t0001g0083a0074c0080t0001g0082others(3): Show | 6 | HG00735.hp2 HG02572.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-4080C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015837 | ||||||
| chr19:17015879
|
G | C | 13 | a0001c0033t0002g0027a0002c0056t0001g0081a0013c0024t0002g0178others(10): Show | 13 | HG00099.hp2 HG00735.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.268-4122C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015879 | ||||||
| chr19:17015955
|
G | A | 2 | a0005c0131t0002g0063a0068c0095t0002g0064 | 2 | NA19088.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.268-4198C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015955 | ||||||
| chr19:17015970
|
C | G | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.268-4213G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17015970 | ||||||
| chr19:17016237
|
C | G | 56 | a0001c0001t0002g0048a0001c0007t0002g0036a0001c0007t0002g0053others(53): Show | 56 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.267+4094G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17016237 | ||||||
| chr19:17016377
|
G | C | 5 | a0001c0013t0001g0138a0007c0119t0001g0122a0023c0075t0001g0137others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+3954C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17016377 | ||||||
| chr19:17016399
|
G | A | 6 | a0002c0017t0001g0162a0042c0174t0001g0160a0088c0047t0001g0161others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.267+3932C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17016399 | ||||||
| chr19:17016591
|
C | T | 142 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0007t0002g0036others(139): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.267+3740G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17016591 | ||||||
| chr19:17017001
|
G | C | 5 | a0002c0056t0001g0081a0045c0051t0001g0083a0074c0080t0001g0082others(2): Show | 5 | HG00735.hp2 HG02572.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+3330C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017001 | ||||||
| chr19:17017094
|
C | T | 1 | a0003c0002t0002g0196 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.267+3237G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017094 | ||||||
| chr19:17017139
|
T | A | 4 | a0021c0037t0002g0190a0038c0099t0002g0224a0050c0148t0002g0235others(1): Show | 4 | HG00438.hp1 NA18949.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+3192A>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017139 | ||||||
| chr19:17017230
|
C | G | 5 | a0001c0013t0001g0138a0007c0119t0001g0122a0023c0075t0001g0137others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+3101G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017230 | ||||||
| chr19:17017295
|
A | C | 29 | a0001c0013t0001g0090a0002c0018t0001g0099a0003c0002t0002g0092others(26): Show | 29 | HG01109.hp1 HG01891.hp1 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.267+3036T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017295 | ||||||
| chr19:17017296
|
T | C | 1 | a0024c0092t0001g0260 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.267+3035A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017296 | ||||||
| chr19:17017318
|
G | T | 6 | a0001c0001t0002g0158a0008c0150t0001g0273a0029c0137t0002g0270others(3): Show | 6 | HG01168.hp2 HG02145.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+3013C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017318 | ||||||
| chr19:17017355
|
A | G | 1 | a0112c0135t0002g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.267+2976T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017355 | ||||||
| chr19:17017357
|
A | G | 153 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0007t0002g0036others(150): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.267+2974T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017357 | ||||||
| chr19:17017386
|
T | C | 2 | a0017c0044t0001g0076a0017c0044t0001g0077 | 2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.267+2945A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017386 | ||||||
| chr19:17017526
|
C | T | 15 | a0005c0003t0002g0125a0006c0006t0001g0131a0006c0015t0002g0133others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.267+2805G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017526 | ||||||
| chr19:17017664
|
G | A | 1 | a0124c0186t0001g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.267+2667C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017664 | ||||||
| chr19:17017907
|
C | T | 1 | a0007c0053t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.267+2424G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17017907 | ||||||
| chr19:17018029
|
T | TA | 36 | a0001c0013t0001g0090a0001c0013t0001g0261a0002c0018t0001g0099others(33): Show | 36 | HG00741.hp2 HG01109.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.267+2301dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018029 | ||||||
| chr19:17018029
|
TA | T | 74 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0007t0002g0036others(71): Show | 74 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.267+2301delT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018029 | ||||||
| chr19:17018171
|
C | T | 1 | a0008c0160t0001g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.267+2160G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018171 | ||||||
| chr19:17018211
|
G | C | 2 | a0005c0131t0002g0063a0068c0095t0002g0064 | 2 | NA19088.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.267+2120C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018211 | ||||||
| chr19:17018298
|
C | T | 1 | a0018c0038t0002g0193 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.267+2033G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018298 | ||||||
| chr19:17018421
|
G | C | 5 | a0010c0004t0001g0068a0057c0073t0001g0066a0069c0098t0001g0065others(2): Show | 5 | HG02615.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+1910C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018421 | ||||||
| chr19:17018431
|
T | C | 5 | a0001c0013t0001g0138a0007c0119t0001g0122a0023c0075t0001g0137others(2): Show | 5 | HG02257.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+1900A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018431 | ||||||
| chr19:17018499
|
T | G | 34 | a0001c0013t0001g0090a0002c0018t0001g0099a0003c0002t0002g0092others(31): Show | 34 | HG00741.hp2 HG01109.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.267+1832A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018499 | ||||||
| chr19:17018693
|
G | A | 5 | a0002c0056t0001g0081a0045c0051t0001g0083a0074c0080t0001g0082others(2): Show | 5 | HG00735.hp2 HG02572.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+1638C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018693 | ||||||
| chr19:17018715
|
A | AAT | 7 | a0020c0011t0001g0017a0020c0011t0001g0020a0034c0070t0002g0091others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.267+1614_267+1615d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018715 | ||||||
| chr19:17018717
|
T | TAC | 27 | a0002c0017t0001g0113a0002c0120t0001g0074a0003c0002t0002g0092others(24): Show | 27 | HG00597.hp1 HG00642.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.267+1612_267+1613d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
T | TACAC | 22 | a0002c0018t0001g0115a0002c0018t0001g0116a0007c0170t0002g0117others(19): Show | 22 | HG02074.hp1 HG02257.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.267+1610_267+1613d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
T | TACACAC | 10 | a0001c0013t0001g0138a0002c0056t0001g0081a0007c0052t0002g0119others(7): Show | 10 | HG01169.hp1 HG01928.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.267+1608_267+1613d others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
T | TACACACA others(1): Show |
8 | a0002c0019t0001g0008a0002c0019t0001g0139a0007c0016t0001g0123others(5): Show | 8 | HG01167.hp1 HG01168.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.267+1606_267+1613d others(10): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
T | TACACACA others(3): Show |
5 | a0001c0013t0001g0090a0007c0016t0001g0124a0007c0119t0001g0122others(2): Show | 5 | HG00735.hp2 HG01169.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.267+1604_267+1613d others(12): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
T | TACACACA others(5): Show |
3 | a0002c0176t0001g0014a0021c0143t0001g0012a0120c0164t0001g0013 | 3 | HG02886.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.267+1602_267+1613d others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
T | TACACACA others(7): Show |
1 | a0061c0142t0002g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.267+1600_267+1613d others(16): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
T | TATAC | 6 | a0002c0018t0001g0099a0020c0011t0001g0021a0028c0114t0001g0100others(3): Show | 6 | HG02055.hp1 HG02055.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+1613_267+1614i others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
TAC | T | 69 | a0001c0001t0002g0147a0001c0001t0002g0248a0001c0001t0002g0266others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.267+1612_267+1613d others(4): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
TACAC | T | 16 | a0001c0001t0002g0158a0005c0003t0002g0125a0005c0131t0002g0063others(13): Show | 16 | HG01168.hp2 HG01175.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.267+1610_267+1613d others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
TACACAC | T | 7 | a0001c0033t0002g0027a0005c0003t0002g0166a0023c0031t0001g0025others(4): Show | 7 | HG00099.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.267+1608_267+1613d others(8): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018717
|
TACACACA others(5): Show |
T | 9 | a0002c0017t0001g0162a0042c0174t0001g0160a0044c0021t0002g0085others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.267+1602_267+1613d others(14): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018717 | ||||||
| chr19:17018829
|
A | G | 1 | a0007c0053t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.267+1502T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018829 | ||||||
| chr19:17018907
|
C | A | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.267+1424G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018907 | ||||||
| chr19:17018918
|
A | AAAAG | 58 | a0001c0001t0002g0048a0001c0007t0002g0036a0001c0007t0002g0053others(55): Show | 58 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.267+1412_267+1413i others(6): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018918 | ||||||
| chr19:17018920
|
G | A | 63 | a0001c0001t0002g0048a0001c0007t0002g0036a0001c0007t0002g0053others(60): Show | 63 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.267+1411C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018920 | ||||||
| chr19:17018920
|
G | GA | 50 | a0001c0001t0002g0266a0002c0017t0001g0112a0002c0017t0001g0113others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.267+1410dupT | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17018920 | ||||||
| chr19:17019293
|
T | C | 1 | a0005c0003t0002g0167 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.267+1038A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019293 | ||||||
| chr19:17019441
|
A | C | 1 | a0002c0019t0001g0139 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.267+890T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019441 | ||||||
| chr19:17019565
|
AT | A | 57 | a0001c0001t0002g0048a0001c0007t0002g0036a0001c0007t0002g0053others(54): Show | 57 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.267+765delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019565 | ||||||
| chr19:17019591
|
T | C | 61 | a0001c0001t0002g0048a0001c0007t0002g0036a0001c0007t0002g0053others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.267+740A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019591 | ||||||
| chr19:17019628
|
T | C | 1 | a0029c0067t0001g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.267+703A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019628 | ||||||
| chr19:17019715
|
C | T | 1 | a0015c0008t0001g0005 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.267+616G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019715 | ||||||
| chr19:17019737
|
A | AT | 14 | a0001c0013t0001g0138a0002c0176t0001g0014a0005c0003t0002g0125others(11): Show | 14 | HG01361.hp1 HG01496.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.267+593dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019737 | ||||||
| chr19:17019737
|
AT | A | 181 | a0001c0001t0002g0147a0001c0001t0002g0158a0001c0001t0002g0185others(178): Show | 181 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.267+593delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019737 | ||||||
| chr19:17019826
|
C | G | 1 | a0032c0043t0001g0191 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.267+505G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019826 | ||||||
| chr19:17019828
|
C | A | 1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.267+503G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019828 | ||||||
| chr19:17019847
|
A | G | 148 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0007t0002g0036others(145): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.267+484T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019847 | ||||||
| chr19:17019931
|
C | T | 33 | a0001c0013t0001g0090a0001c0102t0002g0079a0002c0018t0001g0099others(30): Show | 33 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.267+400G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019931 | ||||||
| chr19:17019953
|
CT | C | 65 | a0001c0001t0002g0048a0001c0007t0002g0036a0001c0007t0002g0053others(62): Show | 65 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.267+377delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019953 | ||||||
| chr19:17019971
|
C | CT | 14 | a0002c0017t0001g0162a0003c0002t0002g0092a0021c0037t0002g0190others(11): Show | 14 | HG01109.hp1 HG01891.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.267+359dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019971 | ||||||
| chr19:17019971
|
CT | C | 5 | a0001c0007t0002g0053a0005c0003t0002g0239a0006c0015t0002g0110others(2): Show | 5 | HG01168.hp2 HG01975.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.267+359delA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019971 | ||||||
| chr19:17019976
|
T | C | 1 | a0002c0019t0001g0139 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.267+355A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17019976 | ||||||
| chr19:17020044
|
G | A | 1 | a0026c0127t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.267+287C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17020044 | ||||||
| chr19:17020060
|
C | T | 49 | a0001c0001t0002g0048a0001c0007t0002g0036a0001c0007t0002g0053others(46): Show | 49 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.267+271G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17020060 | ||||||
| chr19:17020061
|
G | A | 4 | a0001c0013t0001g0138a0023c0075t0001g0137a0047c0046t0002g0135others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+270C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17020061 | ||||||
| chr19:17020133
|
C | T | 1 | a0007c0053t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.267+198G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17020133 | ||||||
| chr19:17020165
|
G | C | 35 | a0001c0013t0001g0090a0001c0102t0002g0079a0002c0018t0001g0099others(32): Show | 35 | HG00741.hp2 HG01109.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.267+166C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17020165 | ||||||
| chr19:17020209
|
G | C | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.267+122C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17020209 | ||||||
| chr19:17020318
|
A | C | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.267+13T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 3/41 | chr19 | 17020318 | ||||||
| chr19:17020501
|
G | A | 1 | a0119c0140t0002g0111 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.245-148C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17020501 | ||||||
| chr19:17020908
|
C | A | 1 | a0001c0013t0001g0138 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.245-555G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17020908 | ||||||
| chr19:17020927
|
CG | C | 7 | a0016c0185t0001g0058a0028c0181t0002g0060a0028c0182t0001g0062others(4): Show | 7 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-575delC | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17020927 | ||||||
| chr19:17020950
|
A | G | 7 | a0001c0013t0001g0138a0002c0056t0001g0081a0023c0075t0001g0137others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.245-597T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17020950 | ||||||
| chr19:17021059
|
C | T | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.245-706G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17021059 | ||||||
| chr19:17021151
|
G | A | 100 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0007t0002g0036others(97): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.245-798C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17021151 | ||||||
| chr19:17021167
|
G | A | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.245-814C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17021167 | ||||||
| chr19:17021179
|
A | C | 23 | a0002c0176t0001g0014a0005c0003t0002g0125a0006c0006t0001g0131others(20): Show | 23 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.245-826T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17021179 | ||||||
| chr19:17021279
|
T | G | 1 | a0007c0119t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.244+751A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17021279 | ||||||
| chr19:17021380
|
C | G | 2 | a0007c0016t0001g0123a0007c0016t0001g0124 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.244+650G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17021380 | ||||||
| chr19:17021388
|
G | C | 2 | a0044c0021t0002g0269a0112c0135t0002g0268 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.244+642C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17021388 | ||||||
| chr19:17021426
|
C | G | 1 | a0100c0068t0002g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.244+604G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17021426 | ||||||
| chr19:17021624
|
A | G | 1 | a0004c0005t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.244+406T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 2/41 | chr19 | 17021624 | ||||||
| chr19:17022185
|
C | T | 1 | a0064c0161t0002g0187 | 1 | HG02683.hp1 | splice_region_variant&intron_variant | LOW | c.93-4G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022185 | ||||||
| chr19:17022218
|
C | A | 15 | a0005c0003t0002g0125a0006c0006t0001g0131a0006c0015t0002g0133others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-37G>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022218 | ||||||
| chr19:17022224
|
C | G | 1 | a0003c0002t0002g0186 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.93-43G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022224 | ||||||
| chr19:17022264
|
C | T | 1 | a0066c0103t0002g0022 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.93-83G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022264 | ||||||
| chr19:17022303
|
G | T | 4 | a0001c0102t0002g0079a0009c0010t0002g0078a0017c0044t0001g0076others(1): Show | 4 | HG02056.hp1 HG02074.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-122C>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022303 | ||||||
| chr19:17022381
|
A | G | 15 | a0005c0003t0002g0125a0006c0006t0001g0131a0006c0015t0002g0133others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-200T>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022381 | ||||||
| chr19:17022456
|
C | T | 1 | a0007c0053t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.93-275G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022456 | ||||||
| chr19:17022494
|
C | CT | 7 | a0002c0017t0001g0162a0042c0174t0001g0160a0088c0047t0001g0161others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.93-314dupA | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022494 | ||||||
| chr19:17022659
|
C | T | 1 | a0042c0175t0001g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.93-478G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022659 | ||||||
| chr19:17022660
|
G | A | 1 | a0004c0100t0002g0054 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.93-479C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022660 | ||||||
| chr19:17022685
|
G | A | 4 | a0001c0013t0001g0138a0023c0075t0001g0137a0047c0046t0002g0135others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.93-504C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022685 | ||||||
| chr19:17022887
|
T | G | 9 | a0002c0019t0001g0139a0016c0185t0001g0058a0028c0181t0002g0060others(6): Show | 9 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.93-706A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022887 | ||||||
| chr19:17022904
|
G | C | 98 | a0001c0001t0002g0048a0001c0001t0002g0158a0001c0007t0002g0036others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.93-723C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022904 | ||||||
| chr19:17022916
|
C | T | 62 | a0001c0001t0002g0147a0001c0001t0002g0185a0001c0001t0002g0248others(59): Show | 62 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.93-735G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022916 | ||||||
| chr19:17022988
|
G | A | 5 | a0010c0004t0001g0068a0057c0073t0001g0066a0069c0098t0001g0065others(2): Show | 5 | HG02615.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-807C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17022988 | ||||||
| chr19:17023226
|
T | C | 2 | a0005c0131t0002g0063a0068c0095t0002g0064 | 2 | NA19088.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.93-1045A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17023226 | ||||||
| chr19:17023233
|
T | C | 1 | a0001c0001t0002g0158 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.93-1052A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17023233 | ||||||
| chr19:17023349
|
T | G | 49 | a0001c0001t0002g0147a0001c0001t0002g0248a0001c0001t0002g0266others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.93-1168A>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17023349 | ||||||
| chr19:17023526
|
A | C | 1 | a0005c0003t0002g0167 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.93-1345T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17023526 | ||||||
| chr19:17023726
|
C | T | 1 | a0002c0019t0001g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93-1545G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17023726 | ||||||
| chr19:17024061
|
C | T | 1 | a0005c0003t0002g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.93-1880G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024061 | ||||||
| chr19:17024164
|
C | T | 5 | a0010c0004t0001g0068a0057c0073t0001g0066a0069c0098t0001g0065others(2): Show | 5 | HG02615.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-1983G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024164 | ||||||
| chr19:17024193
|
C | T | 61 | a0001c0001t0002g0048a0001c0007t0002g0036a0001c0007t0002g0053others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.93-2012G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024193 | ||||||
| chr19:17024367
|
G | C | 8 | a0001c0001t0002g0158a0002c0019t0001g0008a0007c0053t0001g0156others(5): Show | 8 | HG01168.hp2 HG02145.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.92+2184C>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024367 | ||||||
| chr19:17024394
|
A | C | 1 | a0027c0066t0001g0016 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.92+2157T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024394 | ||||||
| chr19:17024417
|
G | A | 7 | a0002c0017t0001g0162a0042c0174t0001g0160a0088c0047t0001g0161others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+2134C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024417 | ||||||
| chr19:17024457
|
T | C | 7 | a0002c0176t0001g0014a0016c0116t0001g0010a0017c0147t0001g0009others(4): Show | 7 | HG01884.hp2 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+2094A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024457 | ||||||
| chr19:17024536
|
G | A | 7 | a0002c0176t0001g0014a0016c0116t0001g0010a0017c0147t0001g0009others(4): Show | 7 | HG01884.hp2 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+2015C>T | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024536 | ||||||
| chr19:17024733
|
C | T | 7 | a0002c0176t0001g0014a0016c0116t0001g0010a0017c0147t0001g0009others(4): Show | 7 | HG01884.hp2 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+1818G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024733 | ||||||
| chr19:17024826
|
T | C | 4 | a0001c0001t0002g0276a0001c0001t0002g0277a0013c0024t0002g0275others(1): Show | 4 | HG01256.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+1725A>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024826 | ||||||
| chr19:17024942
|
C | G | 1 | a0002c0019t0001g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92+1609G>C | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17024942 | ||||||
| chr19:17025864
|
C | T | 1 | a0007c0016t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.92+687G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17025864 | ||||||
| chr19:17026054
|
C | T | 5 | a0001c0033t0002g0002a0015c0008t0001g0005a0029c0067t0001g0004others(2): Show | 5 | HG00741.hp1 HG01515.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+497G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17026054 | ||||||
| chr19:17026368
|
A | C | 1 | a0065c0101t0001g0001 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.92+183T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17026368 | ||||||
| chr19:17026460
|
C | T | 1 | a0038c0109t0002g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.92+91G>A | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17026460 | ||||||
| chr19:17026480
|
A | C | 164 | a0001c0001t0002g0048a0001c0001t0002g0147a0001c0001t0002g0158others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.92+71T>G | CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 1/41 | chr19 | 17026480 |