| geneid | 151903 |
|---|---|
| ensemblid | ENSG00000160799.12 |
| hgncid | 28332 |
| symbol | CCDC12 |
| name | coiled-coil domain containing 12 |
| refseq_nuc | NM_001277074.2 |
| refseq_prot | NP_001264003.1 |
| ensembl_nuc | ENST00000683445.1 |
| ensembl_prot | ENSP00000508011.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 46921730 |
| end | 46976745 |
| strand | - |
| ver | v1.2 |
| region | chr3:46921730-46976745 |
| region5000 | chr3:46916730-46981745 |
| regionname0 | CCDC12_chr3_46921730_46976745 |
| regionname5000 | CCDC12_chr3_46916730_46981745 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 166 | 349 | 87 | 69 | 144 | 10 | 37 | 112 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0002 | 0/0 | 166 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0003 | 0/0 | 166 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| 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 | 0/1 | 501 | 326 | 65 | 69 | 144 | 10 | 37 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| c0002 | 1/0 | 501 | 21 | 20 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| c0003 | 0/0 | 501 | 4 | 1 | 3 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| c0004 | 0/0 | 501 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| c0005 | 0/0 | 501 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 341 | 224 | 74 | 50 | 71 | 6 | 22 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| t0002 | 1/0 | 341 | 130 | 14 | 22 | 73 | 4 | 16 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| 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 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| 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 | 0/1 | 501 | 326 | 65 | 69 | 144 | 10 | 37 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0001c0002 | 1/0 | 501 | 21 | 20 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0001c0004 | 0/0 | 501 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0002c0003 | 0/0 | 501 | 4 | 1 | 3 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0003c0005 | 0/0 | 501 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 841 | 197 | 51 | 47 | 71 | 6 | 21 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0001c0001t0002 | 0/0 | 841 | 129 | 14 | 22 | 73 | 4 | 16 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0001c0002t0001 | 0/0 | 841 | 20 | 20 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0001c0002t0002 | 1/0 | 841 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0001c0004t0001 | 0/0 | 841 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0002c0003t0001 | 0/0 | 841 | 4 | 1 | 3 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| a0003c0005t0001 | 0/0 | 841 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | copy fasta | chr3 | 46916730 | 46981745 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0002t0002g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0004t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0001c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0002c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0002c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| a0003c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | GBR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | GBR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0208 | EUR | FIN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0135 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0158 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0157 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0023 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0018 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03490 | hp2 | a0003 | c0005 | t0001 | g0081 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0149 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | ESN | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | STU | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | BEB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | STU | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | STU | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | STU | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | STU | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | YRI | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | YRI | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | YRI | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | LWK | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | YRI | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ASW | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ASW | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0284 | EUR | TSI | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | GIH | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | GIH | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | USA | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | USA | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | USA | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | USA | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | LWK | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | LWK | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0109 | REF | REF | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0009 | REF | REF | CCDC12_chr3_46916730_46981745 | CCDC12 | chr3 | 46916730 | 46981745 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:46922245
|
C | T | 1 | a0003 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.409G>A | p.Glu137Lys | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 6/7 | 422/841 | 409/501 | 137/166 | chr3 | 46922245 | ||
| chr3:46923621
|
C | T | 1 | a0002 | 4 | HG01106.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
missense_variant | MODERATE | c.292G>A | p.Val98Ile | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 4/7 | 305/841 | 292/501 | 98/166 | chr3 | 46923621 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:46925463
|
C | T | 1 | a0001c0004 | 2 | HG02922.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.237G>A | p.Pro79Pro | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/7 | 250/841 | 237/501 | 79/166 | chr3 | 46925463 | ||
| chr3:46976724
|
T | C | 3 | a0001c0001a0002c0003a0003c0005 | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
synonymous_variant | LOW | c.9A>G | p.Ala3Ala | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/7 | 22/841 | 9/501 | 3/166 | chr3 | 46976724 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:46922012
|
T | C | 5 | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(2): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*45A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 7/7 | 45 | chr3 | 46922012 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:46922201
|
G | T | 1 | a0001c0001t0002g0194 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.418+35C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 6/6 | chr3 | 46922201 | ||||||
| chr3:46922344
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.342-32C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46922344 | ||||||
| chr3:46922349
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.342-37C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46922349 | ||||||
| chr3:46922457
|
C | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.342-145G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46922457 | ||||||
| chr3:46922540
|
C | T | 2 | a0001c0004t0001g0018a0001c0004t0001g0023 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.342-228G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46922540 | ||||||
| chr3:46922697
|
C | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.342-385G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46922697 | ||||||
| chr3:46922816
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.342-504T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46922816 | ||||||
| chr3:46922833
|
C | T | 14 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0318others(11): Show | 14 | HG01109.hp1 HG02451.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.341+496G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46922833 | ||||||
| chr3:46922942
|
G | T | 1 | a0001c0001t0002g0209 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.341+387C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46922942 | ||||||
| chr3:46923245
|
G | A | 4 | a0002c0003t0001g0135a0002c0003t0001g0149a0002c0003t0001g0157others(1): Show | 4 | HG01106.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.341+84C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46923245 | ||||||
| chr3:46923293
|
G | C | 1 | a0001c0001t0002g0312 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.341+36C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46923293 | ||||||
| chr3:46923312
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.341+17C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 5/6 | chr3 | 46923312 | ||||||
| chr3:46923414
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.307-51C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 4/6 | chr3 | 46923414 | ||||||
| chr3:46923490
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.306+117C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 4/6 | chr3 | 46923490 | ||||||
| chr3:46923707
|
C | G | 217 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.245-39G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46923707 | ||||||
| chr3:46923797
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.245-129C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46923797 | ||||||
| chr3:46923912
|
C | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.245-244G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46923912 | ||||||
| chr3:46923948
|
C | T | 2 | a0001c0004t0001g0018a0001c0004t0001g0023 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.245-280G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46923948 | ||||||
| chr3:46924018
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.245-350C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46924018 | ||||||
| chr3:46924029
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.245-361C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46924029 | ||||||
| chr3:46924120
|
T | C | 4 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0004t0001g0018others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-452A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46924120 | ||||||
| chr3:46924366
|
A | G | 217 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.245-698T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46924366 | ||||||
| chr3:46924593
|
C | T | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.244+863G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46924593 | ||||||
| chr3:46924660
|
C | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.244+796G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46924660 | ||||||
| chr3:46924664
|
A | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.244+792T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46924664 | ||||||
| chr3:46924719
|
A | T | 5 | a0001c0001t0001g0173a0001c0001t0001g0337a0001c0002t0001g0012others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+737T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46924719 | ||||||
| chr3:46924897
|
C | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.244+559G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46924897 | ||||||
| chr3:46925408
|
T | C | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG01261.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.244+48A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 3/6 | chr3 | 46925408 | ||||||
| chr3:46925550
|
G | A | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.165-15C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46925550 | ||||||
| chr3:46925581
|
A | G | 2 | a0001c0004t0001g0018a0001c0004t0001g0023 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.165-46T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46925581 | ||||||
| chr3:46925854
|
T | G | 1 | a0001c0001t0002g0236 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.165-319A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46925854 | ||||||
| chr3:46926022
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.165-487C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46926022 | ||||||
| chr3:46926069
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.165-534G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46926069 | ||||||
| chr3:46926232
|
C | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.165-697G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46926232 | ||||||
| chr3:46926234
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.165-699G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46926234 | ||||||
| chr3:46926253
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.165-718C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46926253 | ||||||
| chr3:46926474
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.165-939T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46926474 | ||||||
| chr3:46926533
|
C | G | 7 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(4): Show | 7 | HG01106.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-998G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46926533 | ||||||
| chr3:46926632
|
G | A | 15 | a0001c0001t0001g0173a0001c0001t0001g0337a0001c0002t0001g0001others(12): Show | 19 | HG02055.hp2 HG02145.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.165-1097C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46926632 | ||||||
| chr3:46926737
|
T | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.165-1202A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46926737 | ||||||
| chr3:46926981
|
A | C | 1 | a0001c0001t0001g0324 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.165-1446T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46926981 | ||||||
| chr3:46927109
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.165-1574G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927109 | ||||||
| chr3:46927138
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.165-1603C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927138 | ||||||
| chr3:46927193
|
G | A | 2 | a0001c0004t0001g0018a0001c0004t0001g0023 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.165-1658C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927193 | ||||||
| chr3:46927214
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.165-1679C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927214 | ||||||
| chr3:46927239
|
C | T | 19 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0051others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.165-1704G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927239 | ||||||
| chr3:46927491
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.165-1956C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927491 | ||||||
| chr3:46927568
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.165-2033C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927568 | ||||||
| chr3:46927612
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | NA18943.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.165-2077C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927612 | ||||||
| chr3:46927655
|
C | T | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0314others(9): Show | 12 | HG01106.hp1 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.165-2120G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927655 | ||||||
| chr3:46927680
|
C | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.165-2145G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927680 | ||||||
| chr3:46927694
|
A | G | 5 | a0001c0001t0001g0065a0001c0001t0001g0068a0001c0001t0001g0088others(2): Show | 5 | HG00408.hp2 HG00544.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-2159T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927694 | ||||||
| chr3:46927714
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.165-2179C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927714 | ||||||
| chr3:46927805
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0040others(6): Show | 10 | NA18944.hp2 NA18954.hp1 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.165-2270C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927805 | ||||||
| chr3:46927827
|
G | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.165-2292C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927827 | ||||||
| chr3:46927898
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.165-2363G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927898 | ||||||
| chr3:46927972
|
C | A | 3 | a0001c0001t0002g0006a0001c0001t0002g0236a0001c0001t0002g0242 | 4 | NA18945.hp1 NA18970.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-2437G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46927972 | ||||||
| chr3:46928006
|
T | C | 1 | a0001c0002t0001g0012 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165-2471A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928006 | ||||||
| chr3:46928123
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.165-2588G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928123 | ||||||
| chr3:46928260
|
A | G | 9 | a0001c0001t0002g0172a0001c0001t0002g0186a0001c0001t0002g0253others(6): Show | 9 | HG00558.hp1 HG02015.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.165-2725T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928260 | ||||||
| chr3:46928312
|
G | T | 1 | a0001c0002t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.165-2777C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928312 | ||||||
| chr3:46928397
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.165-2862A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928397 | ||||||
| chr3:46928480
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.165-2945A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928480 | ||||||
| chr3:46928537
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.165-3002T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928537 | ||||||
| chr3:46928741
|
G | A | 12 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0325others(9): Show | 12 | HG01109.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.165-3206C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928741 | ||||||
| chr3:46928820
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.165-3285C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928820 | ||||||
| chr3:46928879
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.165-3344G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928879 | ||||||
| chr3:46928913
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.165-3378C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928913 | ||||||
| chr3:46928919
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165-3384G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46928919 | ||||||
| chr3:46929142
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.165-3607C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929142 | ||||||
| chr3:46929195
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165-3660A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929195 | ||||||
| chr3:46929272
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.165-3737A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929272 | ||||||
| chr3:46929347
|
T | C | 2 | a0001c0004t0001g0018a0001c0004t0001g0023 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.165-3812A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929347 | ||||||
| chr3:46929424
|
C | G | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.165-3889G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929424 | ||||||
| chr3:46929500
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0153 | 2 | NA19064.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.165-3965G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929500 | ||||||
| chr3:46929564
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.165-4029C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929564 | ||||||
| chr3:46929723
|
T | C | 1 | a0001c0001t0001g0109 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.165-4188A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929723 | ||||||
| chr3:46929826
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.165-4291T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929826 | ||||||
| chr3:46929843
|
C | G | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165-4308G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929843 | ||||||
| chr3:46929889
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.165-4354C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929889 | ||||||
| chr3:46929980
|
G | T | 1 | a0001c0001t0002g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.165-4445C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929980 | ||||||
| chr3:46929992
|
C | G | 1 | a0001c0001t0002g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.165-4457G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46929992 | ||||||
| chr3:46930031
|
C | CA | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 135 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.165-4497dupT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46930031 | ||||||
| chr3:46930031
|
C | CAA | 21 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0050others(18): Show | 21 | HG02055.hp1 HG02056.hp2 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.165-4498_165-4497d others(4): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46930031 | ||||||
| chr3:46930031
|
CA | C | 22 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0297others(19): Show | 22 | HG00099.hp1 HG01167.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.165-4497delT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46930031 | ||||||
| chr3:46930140
|
G | T | 3 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0309 | 3 | NA18981.hp2 NA19005.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.165-4605C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46930140 | ||||||
| chr3:46930887
|
T | C | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(211): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.165-5352A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46930887 | ||||||
| chr3:46930952
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.165-5417A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46930952 | ||||||
| chr3:46931154
|
T | C | 2 | a0001c0004t0001g0018a0001c0004t0001g0023 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.165-5619A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931154 | ||||||
| chr3:46931190
|
T | C | 2 | a0001c0004t0001g0018a0001c0004t0001g0023 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.165-5655A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931190 | ||||||
| chr3:46931264
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0310a0001c0001t0001g0311others(2): Show | 5 | HG01891.hp1 HG01934.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.165-5729G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931264 | ||||||
| chr3:46931265
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.165-5730C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931265 | ||||||
| chr3:46931361
|
T | C | 1 | a0001c0001t0002g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.165-5826A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931361 | ||||||
| chr3:46931460
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.165-5925C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931460 | ||||||
| chr3:46931596
|
GC | G | 129 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(126): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.165-6062delG | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931596 | ||||||
| chr3:46931598
|
T | G | 129 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(126): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.165-6063A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931598 | ||||||
| chr3:46931599
|
G | C | 129 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(126): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.165-6064C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931599 | ||||||
| chr3:46931604
|
G | GGAGGGAG others(4): Show |
129 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(126): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.165-6070_165-6069i others(13): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931604 | ||||||
| chr3:46931696
|
C | T | 2 | a0001c0004t0001g0018a0001c0004t0001g0023 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.165-6161G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931696 | ||||||
| chr3:46931830
|
G | T | 2 | a0001c0001t0001g0326a0001c0001t0001g0341 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.165-6295C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931830 | ||||||
| chr3:46931992
|
A | G | 1 | a0001c0001t0002g0312 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.165-6457T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46931992 | ||||||
| chr3:46932081
|
G | A | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG01261.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.165-6546C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932081 | ||||||
| chr3:46932154
|
G | A | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0310others(9): Show | 12 | HG01106.hp1 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.165-6619C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932154 | ||||||
| chr3:46932183
|
T | C | 130 | a0001c0001t0001g0230a0001c0001t0001g0233a0001c0001t0001g0234others(127): Show | 133 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.165-6648A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932183 | ||||||
| chr3:46932315
|
A | G | 1 | a0001c0001t0002g0237 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.165-6780T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932315 | ||||||
| chr3:46932328
|
G | T | 1 | a0001c0001t0002g0242 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.165-6793C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932328 | ||||||
| chr3:46932330
|
G | C | 129 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(126): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.165-6795C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932330 | ||||||
| chr3:46932610
|
G | T | 129 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(126): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.165-7075C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932610 | ||||||
| chr3:46932670
|
T | C | 4 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0002t0001g0024others(1): Show | 4 | HG01891.hp1 HG01934.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-7135A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932670 | ||||||
| chr3:46932670
|
T | G | 2 | a0001c0001t0001g0319a0001c0001t0001g0333 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.165-7135A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932670 | ||||||
| chr3:46932682
|
C | T | 129 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(126): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.165-7147G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932682 | ||||||
| chr3:46932710
|
C | G | 1 | a0001c0001t0002g0191 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.165-7175G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932710 | ||||||
| chr3:46932780
|
A | G | 2 | a0001c0004t0001g0018a0001c0004t0001g0023 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.165-7245T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46932780 | ||||||
| chr3:46933380
|
T | C | 1 | a0001c0001t0002g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.164+7618A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46933380 | ||||||
| chr3:46933539
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164+7459A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46933539 | ||||||
| chr3:46933560
|
C | T | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.164+7438G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46933560 | ||||||
| chr3:46933679
|
G | A | 4 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0002t0001g0024others(1): Show | 4 | HG01891.hp1 HG01934.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+7319C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46933679 | ||||||
| chr3:46933764
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164+7234G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46933764 | ||||||
| chr3:46933811
|
C | T | 4 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0002t0001g0024others(1): Show | 4 | HG01891.hp1 HG01934.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+7187G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46933811 | ||||||
| chr3:46933827
|
G | A | 15 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0320others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.164+7171C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46933827 | ||||||
| chr3:46933898
|
C | A | 1 | a0001c0001t0001g0045 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.164+7100G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46933898 | ||||||
| chr3:46933926
|
A | AT | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.164+7071dupA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46933926 | ||||||
| chr3:46933957
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.164+7041A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46933957 | ||||||
| chr3:46934258
|
C | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.164+6740G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934258 | ||||||
| chr3:46934523
|
C | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.164+6475G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934523 | ||||||
| chr3:46934736
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.164+6262C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934736 | ||||||
| chr3:46934762
|
G | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164+6236C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934762 | ||||||
| chr3:46934764
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.164+6234G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934764 | ||||||
| chr3:46934765
|
C | T | 4 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0002t0001g0024others(1): Show | 4 | HG01891.hp1 HG01934.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+6233G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934765 | ||||||
| chr3:46934810
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164+6188C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934810 | ||||||
| chr3:46934824
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.164+6174A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934824 | ||||||
| chr3:46934895
|
C | T | 2 | a0001c0001t0001g0317a0001c0001t0001g0330 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.164+6103G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934895 | ||||||
| chr3:46934922
|
C | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.164+6076G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934922 | ||||||
| chr3:46934961
|
C | T | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.164+6037G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46934961 | ||||||
| chr3:46935066
|
G | A | 2 | a0001c0004t0001g0018a0001c0004t0001g0023 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.164+5932C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46935066 | ||||||
| chr3:46935187
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.164+5811C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46935187 | ||||||
| chr3:46935323
|
A | C | 1 | a0001c0001t0001g0280 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.164+5675T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46935323 | ||||||
| chr3:46935494
|
C | T | 4 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0002t0001g0024others(1): Show | 4 | HG01891.hp1 HG01934.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+5504G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46935494 | ||||||
| chr3:46935507
|
A | T | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.164+5491T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46935507 | ||||||
| chr3:46935866
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.164+5132C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46935866 | ||||||
| chr3:46935879
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164+5119A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46935879 | ||||||
| chr3:46936048
|
G | A | 334 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(331): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.164+4950C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46936048 | ||||||
| chr3:46936184
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.164+4814G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46936184 | ||||||
| chr3:46936260
|
T | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164+4738A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46936260 | ||||||
| chr3:46936356
|
T | C | 1 | a0001c0001t0001g0331 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.164+4642A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46936356 | ||||||
| chr3:46936374
|
G | C | 1 | a0003c0005t0001g0081 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.164+4624C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46936374 | ||||||
| chr3:46936401
|
C | T | 5 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0137others(2): Show | 5 | HG00735.hp1 HG01081.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+4597G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46936401 | ||||||
| chr3:46936461
|
G | T | 27 | a0001c0001t0002g0006a0001c0001t0002g0156a0001c0001t0002g0166others(24): Show | 28 | HG00408.hp1 HG00558.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.164+4537C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46936461 | ||||||
| chr3:46936660
|
G | A | 1 | a0001c0001t0002g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.164+4338C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46936660 | ||||||
| chr3:46936990
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.164+4008T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46936990 | ||||||
| chr3:46937059
|
T | C | 314 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(311): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.164+3939A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46937059 | ||||||
| chr3:46937175
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0169 | 3 | NA18964.hp1 NA18966.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.164+3823A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46937175 | ||||||
| chr3:46937433
|
A | G | 136 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(133): Show | 137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.164+3565T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46937433 | ||||||
| chr3:46937523
|
G | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.164+3475C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46937523 | ||||||
| chr3:46937739
|
T | G | 2 | a0001c0001t0002g0231a0001c0001t0002g0273 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.164+3259A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46937739 | ||||||
| chr3:46937880
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.164+3118T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46937880 | ||||||
| chr3:46937892
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164+3106C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46937892 | ||||||
| chr3:46938018
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.164+2980G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938018 | ||||||
| chr3:46938195
|
GAA | G | 326 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(323): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.164+2801_164+2802d others(4): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938195 | ||||||
| chr3:46938261
|
T | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.164+2737A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938261 | ||||||
| chr3:46938457
|
C | T | 13 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0232others(10): Show | 13 | HG00558.hp1 HG02015.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.164+2541G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938457 | ||||||
| chr3:46938483
|
T | C | 1 | a0001c0001t0002g0218 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.164+2515A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938483 | ||||||
| chr3:46938518
|
G | GT | 153 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0027others(150): Show | 156 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.164+2479dupA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938518 | ||||||
| chr3:46938518
|
G | GTT | 55 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0055others(52): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.164+2478_164+2479d others(4): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938518 | ||||||
| chr3:46938545
|
G | T | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.164+2453C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938545 | ||||||
| chr3:46938624
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0002g0174a0001c0001t0002g0177others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+2374C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938624 | ||||||
| chr3:46938689
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.164+2309C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938689 | ||||||
| chr3:46938719
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164+2279C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938719 | ||||||
| chr3:46938947
|
A | G | 2 | a0001c0001t0002g0184a0001c0001t0002g0185 | 2 | NA18951.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.164+2051T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46938947 | ||||||
| chr3:46939155
|
G | T | 321 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(318): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.164+1843C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46939155 | ||||||
| chr3:46939371
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.164+1627C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46939371 | ||||||
| chr3:46939377
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.164+1621C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46939377 | ||||||
| chr3:46939517
|
G | C | 1 | a0001c0001t0001g0324 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.164+1481C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46939517 | ||||||
| chr3:46939555
|
C | G | 1 | a0001c0001t0002g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.164+1443G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46939555 | ||||||
| chr3:46939730
|
G | T | 1 | a0001c0001t0002g0259 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+1268C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46939730 | ||||||
| chr3:46939826
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.164+1172C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46939826 | ||||||
| chr3:46939972
|
T | G | 1 | a0001c0001t0002g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.164+1026A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46939972 | ||||||
| chr3:46940154
|
C | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.164+844G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46940154 | ||||||
| chr3:46940572
|
A | G | 328 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(325): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.164+426T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46940572 | ||||||
| chr3:46940684
|
A | T | 1 | a0001c0001t0001g0329 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.164+314T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46940684 | ||||||
| chr3:46940719
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.164+279A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46940719 | ||||||
| chr3:46940765
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.164+233A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46940765 | ||||||
| chr3:46940823
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.164+175G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46940823 | ||||||
| chr3:46940839
|
A | C | 12 | a0001c0001t0002g0034a0001c0001t0002g0159a0001c0001t0002g0174others(9): Show | 12 | HG00544.hp1 HG02258.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.164+159T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46940839 | ||||||
| chr3:46940875
|
T | C | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(321): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.164+123A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 2/6 | chr3 | 46940875 | ||||||
| chr3:46941198
|
C | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0103a0001c0001t0001g0108others(1): Show | 4 | NA18940.hp2 NA18947.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-133G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941198 | ||||||
| chr3:46941219
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.97-154C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941219 | ||||||
| chr3:46941247
|
T | C | 137 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(134): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.97-182A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941247 | ||||||
| chr3:46941272
|
A | G | 326 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(323): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.97-207T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941272 | ||||||
| chr3:46941283
|
C | G | 137 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(134): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.97-218G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941283 | ||||||
| chr3:46941284
|
T | C | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-219A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941284 | ||||||
| chr3:46941289
|
G | A | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-224C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941289 | ||||||
| chr3:46941343
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.97-278A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941343 | ||||||
| chr3:46941345
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97-280C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941345 | ||||||
| chr3:46941379
|
G | A | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-314C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941379 | ||||||
| chr3:46941408
|
C | A | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.97-343G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941408 | ||||||
| chr3:46941482
|
G | A | 1 | a0001c0001t0001g0330 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.97-417C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941482 | ||||||
| chr3:46941497
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-432T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941497 | ||||||
| chr3:46941564
|
CA | C | 326 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(323): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.97-500delT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941564 | ||||||
| chr3:46941568
|
A | G | 1 | a0001c0001t0002g0246 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.97-503T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941568 | ||||||
| chr3:46941713
|
CAGGCCAG others(19): Show |
C | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.97-674_97-649delAG others(24): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941713 | ||||||
| chr3:46941798
|
G | A | 13 | a0001c0001t0001g0167a0001c0001t0001g0266a0001c0001t0001g0267others(10): Show | 15 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.97-733C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941798 | ||||||
| chr3:46941820
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.97-755G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941820 | ||||||
| chr3:46941958
|
G | A | 1 | a0001c0001t0002g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.97-893C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46941958 | ||||||
| chr3:46942040
|
C | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-975G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46942040 | ||||||
| chr3:46942161
|
A | C | 329 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(326): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.97-1096T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46942161 | ||||||
| chr3:46942225
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.97-1160C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46942225 | ||||||
| chr3:46942353
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0002g0284 | 2 | HG00738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.97-1288G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46942353 | ||||||
| chr3:46942401
|
A | G | 329 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(326): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.97-1336T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46942401 | ||||||
| chr3:46942646
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-1581C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46942646 | ||||||
| chr3:46942803
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.97-1738A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46942803 | ||||||
| chr3:46942877
|
G | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-1812C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46942877 | ||||||
| chr3:46943209
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-2144G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46943209 | ||||||
| chr3:46943235
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-2170C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46943235 | ||||||
| chr3:46943405
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.97-2340C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46943405 | ||||||
| chr3:46943642
|
T | C | 295 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.97-2577A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46943642 | ||||||
| chr3:46943768
|
G | C | 6 | a0001c0001t0001g0122a0001c0001t0001g0294a0001c0001t0001g0295others(3): Show | 6 | HG00099.hp1 HG01496.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-2703C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46943768 | ||||||
| chr3:46943889
|
A | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.97-2824T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46943889 | ||||||
| chr3:46944002
|
A | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0168 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.97-2937T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46944002 | ||||||
| chr3:46944102
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.97-3037G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46944102 | ||||||
| chr3:46944153
|
G | C | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-3088C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46944153 | ||||||
| chr3:46944272
|
G | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-3207C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46944272 | ||||||
| chr3:46944322
|
T | C | 1 | a0001c0001t0002g0216 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.97-3257A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46944322 | ||||||
| chr3:46944361
|
C | A | 1 | a0001c0001t0002g0224 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.97-3296G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46944361 | ||||||
| chr3:46944373
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-3308T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46944373 | ||||||
| chr3:46944560
|
C | T | 321 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(318): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.97-3495G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46944560 | ||||||
| chr3:46944839
|
G | A | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.97-3774C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46944839 | ||||||
| chr3:46944844
|
A | G | 1 | a0001c0001t0001g0290 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.97-3779T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46944844 | ||||||
| chr3:46945553
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-4488G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46945553 | ||||||
| chr3:46945935
|
C | CT | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | HG02258.hp1 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.97-4871dupA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46945935 | ||||||
| chr3:46946151
|
C | T | 329 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(326): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.97-5086G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946151 | ||||||
| chr3:46946260
|
G | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-5195C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946260 | ||||||
| chr3:46946464
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.97-5399G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946464 | ||||||
| chr3:46946492
|
T | A | 1 | a0001c0001t0001g0042 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.97-5427A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946492 | ||||||
| chr3:46946747
|
G | C | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.97-5682C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946747 | ||||||
| chr3:46946774
|
G | T | 1 | a0001c0001t0001g0331 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.97-5709C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946774 | ||||||
| chr3:46946844
|
A | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-5779T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946844 | ||||||
| chr3:46946866
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-5801G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946866 | ||||||
| chr3:46946916
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-5851T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946916 | ||||||
| chr3:46946967
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-5902C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946967 | ||||||
| chr3:46946991
|
G | A | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.97-5926C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46946991 | ||||||
| chr3:46947071
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.97-6006G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46947071 | ||||||
| chr3:46947164
|
C | T | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.97-6099G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46947164 | ||||||
| chr3:46947275
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-6210A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46947275 | ||||||
| chr3:46947411
|
G | A | 2 | a0001c0001t0002g0195a0001c0001t0002g0204 | 2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.97-6346C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46947411 | ||||||
| chr3:46947503
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.97-6438T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46947503 | ||||||
| chr3:46947537
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-6472T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46947537 | ||||||
| chr3:46947664
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.97-6599C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46947664 | ||||||
| chr3:46947672
|
T | C | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-6607A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46947672 | ||||||
| chr3:46948028
|
C | T | 31 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0316others(28): Show | 31 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.97-6963G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948028 | ||||||
| chr3:46948267
|
T | G | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-7202A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948267 | ||||||
| chr3:46948338
|
C | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.97-7273G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948338 | ||||||
| chr3:46948346
|
G | A | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-7281C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948346 | ||||||
| chr3:46948374
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97-7309C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948374 | ||||||
| chr3:46948376
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-7311A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948376 | ||||||
| chr3:46948414
|
G | A | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.97-7349C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948414 | ||||||
| chr3:46948814
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.97-7749C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948814 | ||||||
| chr3:46948846
|
T | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-7781A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948846 | ||||||
| chr3:46948900
|
C | T | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.97-7835G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948900 | ||||||
| chr3:46948921
|
C | T | 1 | a0001c0002t0001g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.97-7856G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948921 | ||||||
| chr3:46948930
|
GGTACTCC others(9): Show |
G | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-7881_97-7866del others(16): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948930 | ||||||
| chr3:46948947
|
T | C | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-7882A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948947 | ||||||
| chr3:46948981
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97-7916C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948981 | ||||||
| chr3:46948986
|
G | A | 4 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0002t0001g0024others(1): Show | 4 | HG01891.hp1 HG04115.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-7921C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46948986 | ||||||
| chr3:46949019
|
G | A | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-7954C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949019 | ||||||
| chr3:46949052
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.97-7987A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949052 | ||||||
| chr3:46949057
|
G | T | 1 | a0001c0001t0002g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.97-7992C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949057 | ||||||
| chr3:46949076
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.97-8011G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949076 | ||||||
| chr3:46949183
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.97-8118C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949183 | ||||||
| chr3:46949246
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.97-8181A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949246 | ||||||
| chr3:46949428
|
C | T | 20 | a0001c0001t0001g0122a0001c0001t0001g0289a0001c0001t0001g0290others(17): Show | 20 | HG00099.hp1 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-8363G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949428 | ||||||
| chr3:46949446
|
C | G | 1 | a0001c0001t0002g0313 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.97-8381G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949446 | ||||||
| chr3:46949574
|
T | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-8509A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949574 | ||||||
| chr3:46949652
|
T | C | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.97-8587A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949652 | ||||||
| chr3:46949716
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.97-8651G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949716 | ||||||
| chr3:46949751
|
G | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.97-8686C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949751 | ||||||
| chr3:46949789
|
G | T | 1 | a0003c0005t0001g0081 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.97-8724C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949789 | ||||||
| chr3:46949825
|
G | A | 1 | a0001c0002t0001g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.97-8760C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949825 | ||||||
| chr3:46949900
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.97-8835C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949900 | ||||||
| chr3:46949946
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.97-8881C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949946 | ||||||
| chr3:46949982
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.97-8917G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46949982 | ||||||
| chr3:46950025
|
CA | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.97-8961delT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950025 | ||||||
| chr3:46950031
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0292 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.97-8982_97-8967del others(16): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950031 | ||||||
| chr3:46950043
|
A | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.97-8978T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950043 | ||||||
| chr3:46950104
|
G | A | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-9039C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950104 | ||||||
| chr3:46950194
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-9129T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950194 | ||||||
| chr3:46950315
|
A | AT | 321 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(318): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.97-9251dupA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950315 | ||||||
| chr3:46950336
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-9271C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950336 | ||||||
| chr3:46950364
|
A | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-9299T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950364 | ||||||
| chr3:46950493
|
T | TG | 4 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0092others(1): Show | 4 | HG01884.hp2 HG03654.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-9429_97-9428ins others(1): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950493 | ||||||
| chr3:46950494
|
T | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-9429A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950494 | ||||||
| chr3:46950494
|
T | TG | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(136): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.97-9430_97-9429ins others(1): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950494 | ||||||
| chr3:46950495
|
T | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.97-9430A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950495 | ||||||
| chr3:46950495
|
T | TG | 173 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(170): Show | 173 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.97-9431_97-9430ins others(1): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950495 | ||||||
| chr3:46950496
|
T | G | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.97-9431A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950496 | ||||||
| chr3:46950496
|
T | TGG | 5 | a0001c0001t0001g0293a0001c0001t0001g0337a0001c0001t0002g0162others(2): Show | 5 | HG01346.hp2 HG02572.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-9433_97-9432dup others(2): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950496 | ||||||
| chr3:46950782
|
T | C | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-9717A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46950782 | ||||||
| chr3:46951415
|
C | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-10350G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951415 | ||||||
| chr3:46951446
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-10381T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951446 | ||||||
| chr3:46951518
|
G | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-10453C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951518 | ||||||
| chr3:46951538
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.97-10473A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951538 | ||||||
| chr3:46951637
|
G | A | 141 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(138): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.97-10572C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951637 | ||||||
| chr3:46951653
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-10588T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951653 | ||||||
| chr3:46951726
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.97-10661C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951726 | ||||||
| chr3:46951759
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.97-10694C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951759 | ||||||
| chr3:46951779
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0068a0001c0001t0001g0088 | 2 | HG00544.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.97-10725_97-10715d others(13): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951779 | ||||||
| chr3:46951779
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0115a0001c0001t0001g0155a0001c0001t0002g0085 | 3 | HG03942.hp2 NA18946.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.97-10726_97-10715d others(14): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951779 | ||||||
| chr3:46951779
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0099others(5): Show | 9 | HG01358.hp2 HG02135.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-10727_97-10715d others(15): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951779 | ||||||
| chr3:46951779
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0038a0001c0001t0002g0153 | 2 | NA18968.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.97-10728_97-10715d others(16): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951779 | ||||||
| chr3:46951792
|
A | ATAT | 8 | a0001c0001t0001g0267a0001c0001t0001g0270a0001c0001t0001g0271others(5): Show | 9 | HG00140.hp1 HG00735.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-10728_97-10727i others(5): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951792 | ||||||
| chr3:46951792
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.97-10727T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951792 | ||||||
| chr3:46951794
|
A | T | 11 | a0001c0001t0001g0167a0001c0001t0001g0266a0001c0001t0001g0267others(8): Show | 13 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-10729T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951794 | ||||||
| chr3:46951796
|
A | T | 13 | a0001c0001t0001g0167a0001c0001t0001g0266a0001c0001t0001g0267others(10): Show | 15 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.97-10731T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951796 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(27): Show |
2 | a0001c0001t0002g0248a0001c0001t0002g0255 | 2 | NA18960.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(36): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0002g0258 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(31): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(24): Show |
2 | a0001c0001t0001g0262a0001c0001t0002g0242 | 2 | NA18956.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(33): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0232 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(30): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0002g0006a0001c0001t0002g0236 | 3 | NA18945.hp1 NA19005.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(32): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(37): Show |
1 | a0001c0001t0002g0313 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(46): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0036a0001c0001t0002g0257 | 2 | HG00558.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(31): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0251 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(33): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0035a0001c0001t0002g0256 | 2 | NA18995.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(30): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(25): Show |
3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0002g0252 | 3 | HG02258.hp1 HG03471.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(34): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0002g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(38): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0002g0182 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(40): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0002g0186a0001c0001t0002g0254 | 2 | NA19079.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(31): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0002g0265 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(33): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0002g0159 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(41): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0241a0001c0001t0002g0253 | 2 | HG02015.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(30): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0002g0250a0001c0001t0002g0275 | 2 | NA18965.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(32): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0001g0235 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(36): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(33): Show |
2 | a0001c0001t0001g0311a0001c0001t0002g0204 | 2 | HG02486.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(42): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(20): Show |
2 | a0001c0001t0002g0247a0001c0001t0002g0261 | 2 | NA18988.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(29): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(24): Show |
2 | a0001c0001t0002g0034a0001c0001t0002g0172 | 2 | NA18941.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(33): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(28): Show |
2 | a0001c0001t0001g0310a0001c0001t0002g0237 | 2 | HG01934.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(37): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0002g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(41): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(42): Show |
1 | a0001c0001t0002g0187 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(51): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0067 | 2 | HG02004.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(22): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0331 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(26): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(28): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0240a0001c0001t0002g0260 | 2 | HG02074.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(30): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(38): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0002g0288 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(40): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(16): Show |
3 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0001g0338 | 3 | HG02572.hp2 HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(25): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(20): Show |
5 | a0001c0001t0002g0180a0001c0001t0002g0226a0001c0001t0002g0239others(2): Show | 5 | HG01981.hp1 HG02004.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(29): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(24): Show |
2 | a0001c0001t0002g0193a0001c0001t0002g0264 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(33): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0002g0160 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(35): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0002g0195 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(37): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(34): Show |
1 | a0001c0001t0002g0185 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(43): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0041 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(18): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(13): Show |
2 | a0002c0003t0001g0157a0002c0003t0001g0158 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(22): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0327 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(24): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(17): Show |
3 | a0001c0001t0001g0136a0001c0001t0001g0330a0001c0001t0002g0192 | 3 | HG03688.hp2 NA18612.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(26): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(21): Show |
3 | a0001c0001t0001g0342a0001c0001t0002g0245a0001c0001t0002g0312 | 3 | HG01952.hp2 NA18952.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(30): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0002g0037a0001c0001t0002g0206 | 2 | HG02280.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(32): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0002g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(34): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0002g0276 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(38): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0002g0194 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(40): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(37): Show |
1 | a0001c0001t0002g0184 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(46): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0063 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(17): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0339 | 2 | HG02015.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(23): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(16): Show |
6 | a0001c0001t0001g0317a0001c0001t0001g0321a0001c0001t0001g0323others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(25): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(18): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0319a0001c0001t0001g0340 | 3 | HG02897.hp1 HG03579.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(27): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(20): Show |
6 | a0001c0001t0001g0329a0001c0001t0001g0343a0001c0001t0001g0344others(3): Show | 6 | HG01928.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(29): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(22): Show |
3 | a0001c0001t0001g0336a0001c0001t0002g0277a0001c0001t0002g0282 | 3 | HG02922.hp2 HG03654.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(31): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(24): Show |
3 | a0001c0001t0001g0335a0001c0001t0002g0196a0001c0001t0002g0273 | 3 | HG01109.hp1 HG03471.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(33): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0002g0281 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(35): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(28): Show |
2 | a0001c0001t0002g0046a0001c0001t0002g0203 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(37): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0002g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(41): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(7): Show |
8 | a0001c0001t0001g0047a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 8 | HG00597.hp2 HG00609.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(16): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(11): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0118a0001c0001t0002g0044 | 3 | HG03927.hp2 NA19064.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(20): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0110 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(22): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0002g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(24): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(17): Show |
6 | a0001c0001t0001g0108a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 6 | HG00280.hp2 HG01081.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(26): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0002g0238 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(28): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0002g0179 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(30): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(23): Show |
3 | a0001c0001t0001g0077a0001c0001t0002g0190a0001c0001t0002g0283 | 3 | HG04228.hp2 NA19066.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(32): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(25): Show |
2 | a0001c0001t0002g0205a0001c0001t0002g0221 | 2 | HG01109.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(34): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(27): Show |
2 | a0001c0001t0002g0181a0001c0001t0002g0244 | 2 | HG02080.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(36): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0002g0249 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(38): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(33): Show |
1 | a0001c0001t0002g0201 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(42): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(6): Show |
21 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0065others(18): Show | 21 | HG00280.hp1 HG00408.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(15): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(8): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0059a0001c0001t0001g0074others(3): Show | 7 | HG01975.hp1 HG01993.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(17): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(10): Show |
3 | a0001c0001t0001g0073a0001c0001t0001g0092a0003c0005t0001g0081 | 3 | HG00738.hp2 HG03490.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(19): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(23): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(16): Show |
6 | a0001c0001t0001g0033a0001c0001t0001g0126a0001c0001t0001g0140others(3): Show | 6 | HG01891.hp2 HG01928.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(25): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(18): Show |
2 | a0001c0001t0002g0197a0001c0001t0002g0207 | 2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(27): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0002g0224 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(29): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(22): Show |
5 | a0001c0001t0002g0162a0001c0001t0002g0176a0001c0001t0002g0219others(2): Show | 5 | HG00621.hp2 HG01167.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(31): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(24): Show |
4 | a0001c0001t0001g0089a0001c0001t0001g0148a0001c0001t0002g0213others(1): Show | 4 | HG02080.hp1 HG04228.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(33): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0002g0217 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(35): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0002g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(37): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(30): Show |
2 | a0001c0001t0002g0177a0001c0001t0002g0202 | 2 | HG00609.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(39): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0002g0215 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(41): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(36): Show |
1 | a0001c0001t0002g0191 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(45): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(5): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0132a0001c0001t0001g0142 | 3 | HG00673.hp1 HG01257.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(14): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(7): Show |
7 | a0001c0001t0001g0131a0001c0001t0001g0150a0001c0001t0001g0170others(4): Show | 7 | HG01346.hp1 HG01943.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(16): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(9): Show |
3 | a0001c0001t0001g0057a0001c0001t0001g0079a0001c0001t0001g0091 | 3 | HG00741.hp1 HG02273.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(18): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0133 | 2 | HG01952.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(22): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0107 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(24): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(17): Show |
3 | a0001c0001t0001g0078a0001c0001t0001g0128a0001c0001t0001g0325 | 3 | HG01070.hp1 HG03041.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(26): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0064a0001c0001t0002g0199 | 2 | HG04199.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(28): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(30): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(23): Show |
3 | a0001c0001t0001g0103a0001c0001t0002g0026a0001c0001t0002g0188 | 3 | HG02083.hp1 NA18947.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(32): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(25): Show |
2 | a0001c0001t0002g0227a0001c0001t0002g0278 | 2 | HG01496.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(34): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(27): Show |
2 | a0001c0001t0002g0183a0001c0001t0002g0231 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(36): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0002g0216 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(38): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(6): Show |
9 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0112others(6): Show | 9 | HG00642.hp1 HG01081.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(15): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(8): Show |
5 | a0001c0001t0001g0056a0001c0001t0001g0090a0001c0001t0001g0171others(2): Show | 5 | HG01496.hp2 HG01993.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(17): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(10): Show |
2 | a0001c0001t0001g0076a0001c0001t0001g0302 | 2 | HG00621.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(19): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(14): Show |
3 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0002g0284 | 3 | NA18906.hp2 NA18951.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(23): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(16): Show |
7 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0084others(4): Show | 7 | HG00639.hp1 HG01074.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(25): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(18): Show |
2 | a0001c0001t0001g0106a0001c0001t0001g0230 | 2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(27): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(24): Show |
2 | a0001c0001t0002g0225a0001c0001t0002g0287 | 2 | HG02132.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(33): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0001g0324 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(35): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0002g0200 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(39): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(14): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(7): Show |
2 | a0001c0001t0001g0297a0001c0001t0001g0305 | 2 | HG00099.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(16): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0315 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(18): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0002g0209 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(20): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0071 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(22): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0001g0055a0001c0001t0001g0086 | 2 | HG02738.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(24): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(17): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0129 | 2 | HG01071.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(26): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0070 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(28): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0002g0164a0001c0001t0002g0178 | 2 | NA18949.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(32): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(16): Show |
2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(25): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(6): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0123 | 2 | HG00140.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(15): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(10): Show |
3 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0151 | 4 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-10734_97-10733i others(19): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(16): Show |
2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(25): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0002g0189 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(31): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(7): Show |
2 | a0001c0001t0001g0314a0001c0001t0002g0166 | 2 | HG00408.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.97-10734_97-10733i others(16): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0062 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(22): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(24): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(32): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAT others(4): Show |
1 | a0002c0003t0001g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(13): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAT others(6): Show |
1 | a0001c0001t0002g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(15): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAT others(12): Show |
1 | a0001c0001t0001g0125 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.97-10734_97-10733i others(21): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAAAT others(24): Show |
1 | a0001c0001t0002g0286 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(33): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAATA others(9): Show |
1 | a0001c0001t0001g0332 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(18): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AAAAAATA others(13): Show |
1 | a0002c0003t0001g0135 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.97-10734_97-10733i others(22): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-10749_97-10734d others(18): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951798
|
A | T | 17 | a0001c0001t0001g0167a0001c0001t0001g0266a0001c0001t0001g0267others(14): Show | 19 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.97-10733T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951798 | ||||||
| chr3:46951800
|
T | A | 12 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0102others(9): Show | 12 | HG01261.hp2 HG02056.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.97-10735A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951800 | ||||||
| chr3:46951802
|
T | A | 5 | a0001c0001t0001g0124a0001c0001t0001g0173a0001c0001t0001g0285others(2): Show | 5 | HG02145.hp1 HG03017.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-10737A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951802 | ||||||
| chr3:46951804
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97-10739A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951804 | ||||||
| chr3:46951824
|
C | T | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(321): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.97-10759G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951824 | ||||||
| chr3:46951825
|
T | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.97-10760A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951825 | ||||||
| chr3:46951826
|
T | A | 1 | a0003c0005t0001g0081 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.97-10761A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46951826 | ||||||
| chr3:46952217
|
G | C | 1 | a0001c0001t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.97-11152C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46952217 | ||||||
| chr3:46952297
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.97-11232C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46952297 | ||||||
| chr3:46952425
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-11360C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46952425 | ||||||
| chr3:46952753
|
A | G | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-11688T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46952753 | ||||||
| chr3:46953167
|
C | A | 1 | a0001c0001t0001g0126 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.97-12102G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953167 | ||||||
| chr3:46953328
|
A | G | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-12263T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953328 | ||||||
| chr3:46953413
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-12348T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953413 | ||||||
| chr3:46953436
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.97-12371C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953436 | ||||||
| chr3:46953497
|
G | A | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.97-12432C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953497 | ||||||
| chr3:46953648
|
G | GA | 7 | a0001c0001t0001g0126a0001c0001t0001g0145a0001c0001t0001g0266others(4): Show | 7 | HG02080.hp1 HG02738.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-12584dupT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953648 | ||||||
| chr3:46953679
|
T | C | 2 | a0001c0001t0002g0177a0001c0001t0002g0183 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.97-12614A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953679 | ||||||
| chr3:46953697
|
G | A | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-12632C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953697 | ||||||
| chr3:46953718
|
G | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0088 | 2 | HG00544.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.97-12653C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953718 | ||||||
| chr3:46953752
|
C | T | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.97-12687G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953752 | ||||||
| chr3:46953813
|
G | T | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-12748C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953813 | ||||||
| chr3:46953850
|
A | G | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-12785T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46953850 | ||||||
| chr3:46954116
|
CAG | C | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.97-13053_97-13052d others(4): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46954116 | ||||||
| chr3:46954439
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.97-13374G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46954439 | ||||||
| chr3:46954509
|
C | T | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(317): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.97-13444G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46954509 | ||||||
| chr3:46954659
|
TCACGCCT others(11): Show |
T | 13 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0325others(10): Show | 13 | HG01109.hp1 HG02572.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-13612_97-13595d others(20): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46954659 | ||||||
| chr3:46954696
|
C | A | 3 | a0001c0001t0001g0317a0001c0001t0001g0330a0001c0001t0001g0331 | 3 | HG03139.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.97-13631G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46954696 | ||||||
| chr3:46954696
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-13631G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46954696 | ||||||
| chr3:46954713
|
T | G | 1 | a0001c0001t0002g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.97-13648A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46954713 | ||||||
| chr3:46954810
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.97-13745C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46954810 | ||||||
| chr3:46954952
|
C | T | 180 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(177): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.97-13887G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46954952 | ||||||
| chr3:46954958
|
A | G | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.97-13893T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46954958 | ||||||
| chr3:46955105
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.97-14040C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955105 | ||||||
| chr3:46955201
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG00735.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.97-14136G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955201 | ||||||
| chr3:46955219
|
T | TC | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-14155dupG | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955219 | ||||||
| chr3:46955250
|
CA | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0102others(3): Show | 7 | NA18944.hp2 NA18954.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-14186delT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955250 | ||||||
| chr3:46955469
|
C | T | 1 | a0001c0001t0002g0236 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.97-14404G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955469 | ||||||
| chr3:46955475
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-14410T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955475 | ||||||
| chr3:46955531
|
C | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.97-14466G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955531 | ||||||
| chr3:46955569
|
G | A | 13 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0325others(10): Show | 13 | HG01109.hp1 HG02572.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-14504C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955569 | ||||||
| chr3:46955584
|
G | A | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-14519C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955584 | ||||||
| chr3:46955734
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.97-14669C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955734 | ||||||
| chr3:46955758
|
G | A | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-14693C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955758 | ||||||
| chr3:46955777
|
A | G | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.97-14712T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955777 | ||||||
| chr3:46955944
|
G | A | 2 | a0001c0001t0002g0249a0001c0001t0002g0274 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.97-14879C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955944 | ||||||
| chr3:46955952
|
G | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-14887C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46955952 | ||||||
| chr3:46956339
|
T | C | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-15274A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46956339 | ||||||
| chr3:46956368
|
G | A | 7 | a0001c0001t0002g0176a0001c0001t0002g0221a0001c0001t0002g0222others(4): Show | 7 | HG00621.hp2 NA18948.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-15303C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46956368 | ||||||
| chr3:46956560
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.97-15495C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46956560 | ||||||
| chr3:46956764
|
T | TGAGCC | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-15700_97-15699i others(7): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46956764 | ||||||
| chr3:46956790
|
T | C | 1 | a0001c0001t0002g0189 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.97-15725A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46956790 | ||||||
| chr3:46956831
|
C | CG | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.97-15767_97-15766i others(3): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46956831 | ||||||
| chr3:46956833
|
C | A | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-15768G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46956833 | ||||||
| chr3:46956845
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.97-15780G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46956845 | ||||||
| chr3:46957008
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.97-15943C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957008 | ||||||
| chr3:46957015
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.97-15950A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957015 | ||||||
| chr3:46957071
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-16006A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957071 | ||||||
| chr3:46957307
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-16242C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957307 | ||||||
| chr3:46957494
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.97-16429G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957494 | ||||||
| chr3:46957563
|
C | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-16498G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957563 | ||||||
| chr3:46957588
|
A | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-16523T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957588 | ||||||
| chr3:46957595
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-16530T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957595 | ||||||
| chr3:46957611
|
G | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-16546C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957611 | ||||||
| chr3:46957624
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.97-16559T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957624 | ||||||
| chr3:46957688
|
T | C | 2 | a0002c0003t0001g0157a0002c0003t0001g0158 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.97-16623A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957688 | ||||||
| chr3:46957708
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-16643T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957708 | ||||||
| chr3:46957772
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97-16707A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957772 | ||||||
| chr3:46957806
|
G | A | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-16741C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957806 | ||||||
| chr3:46957958
|
A | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.97-16893T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957958 | ||||||
| chr3:46957960
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.97-16895A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957960 | ||||||
| chr3:46957960
|
T | TAC | 5 | a0001c0001t0001g0310a0001c0001t0002g0250a0001c0001t0002g0274others(2): Show | 5 | HG01934.hp1 HG02622.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-16897_97-16896d others(4): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957960 | ||||||
| chr3:46957960
|
T | TACAC | 6 | a0001c0001t0001g0035a0001c0001t0001g0122a0001c0001t0001g0251others(3): Show | 6 | HG02148.hp2 HG02486.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-16899_97-16896d others(6): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957960 | ||||||
| chr3:46957960
|
T | TACACAC | 26 | a0001c0001t0001g0036a0001c0001t0001g0233a0001c0001t0001g0240others(23): Show | 27 | HG00408.hp1 HG00558.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.97-16901_97-16896d others(8): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957960 | ||||||
| chr3:46957960
|
T | TACACACA others(1): Show |
17 | a0001c0001t0001g0127a0001c0001t0001g0232a0001c0001t0001g0262others(14): Show | 17 | HG01106.hp1 HG01123.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.97-16903_97-16896d others(10): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957960 | ||||||
| chr3:46957960
|
T | TACACACA others(3): Show |
4 | a0001c0001t0001g0173a0001c0001t0001g0234a0001c0001t0002g0037others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-16905_97-16896d others(12): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957960 | ||||||
| chr3:46957960
|
T | TACACACA others(5): Show |
6 | a0001c0001t0001g0235a0001c0001t0001g0326a0001c0001t0002g0007others(3): Show | 8 | HG00735.hp2 HG01255.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-16907_97-16896d others(14): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957960 | ||||||
| chr3:46957960
|
T | TACACACA others(7): Show |
7 | a0001c0001t0001g0167a0001c0001t0001g0230a0001c0001t0002g0060others(4): Show | 7 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-16909_97-16896d others(16): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957960 | ||||||
| chr3:46957960
|
TAC | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-16897_97-16896d others(4): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957960 | ||||||
| chr3:46957960
|
TACACAC | T | 5 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0269others(2): Show | 5 | HG01192.hp1 HG01884.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-16901_97-16896d others(8): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957960 | ||||||
| chr3:46957970
|
C | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.97-16905G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957970 | ||||||
| chr3:46957994
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.97-16929G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957994 | ||||||
| chr3:46957996
|
C | CACACACA others(15): Show |
1 | a0001c0001t0002g0227 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.97-16932_97-16931i others(24): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | CACACACA others(13): Show |
6 | a0001c0001t0002g0162a0001c0001t0002g0176a0001c0001t0002g0225others(3): Show | 6 | HG01346.hp2 HG02132.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-16932_97-16931i others(22): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | CACACACA others(11): Show |
2 | a0001c0001t0002g0192a0001c0001t0002g0224 | 2 | HG01975.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.97-16932_97-16931i others(20): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | CACACACA others(9): Show |
19 | a0001c0001t0002g0026a0001c0001t0002g0160a0001c0001t0002g0161others(16): Show | 19 | HG00621.hp2 HG00673.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.97-16932_97-16931i others(18): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | CACACACA others(7): Show |
22 | a0001c0001t0002g0046a0001c0001t0002g0164a0001c0001t0002g0175others(19): Show | 22 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-16932_97-16931i others(16): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | CACACACA others(5): Show |
12 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0340others(9): Show | 12 | HG00639.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-16932_97-16931i others(14): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | CACACACA others(3): Show |
31 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0067others(28): Show | 31 | HG00735.hp1 HG01109.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-16932_97-16931i others(12): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | CACACACA others(1): Show |
60 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0028others(57): Show | 62 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.97-16932_97-16931i others(10): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | CACACACA others(3): Show |
1 | a0001c0001t0001g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.97-16932_97-16931i others(12): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | CACACAT | 72 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0040others(69): Show | 73 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.97-16932_97-16931i others(8): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | CACAT | 16 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0055others(13): Show | 16 | HG00544.hp2 HG00597.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.97-16932_97-16931i others(6): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957996
|
C | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-16931G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957996 | ||||||
| chr3:46957998
|
T | C | 3 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0002g0037 | 3 | HG01934.hp1 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.97-16933A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46957998 | ||||||
| chr3:46958217
|
C | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.97-17152G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958217 | ||||||
| chr3:46958218
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.97-17153C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958218 | ||||||
| chr3:46958361
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-17296A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958361 | ||||||
| chr3:46958364
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.97-17299A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958364 | ||||||
| chr3:46958419
|
A | G | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.97-17354T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958419 | ||||||
| chr3:46958513
|
T | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.97-17448A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958513 | ||||||
| chr3:46958538
|
G | A | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-17473C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958538 | ||||||
| chr3:46958636
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.97-17571A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958636 | ||||||
| chr3:46958654
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.97-17589G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958654 | ||||||
| chr3:46958701
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0076 | 2 | HG01106.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.97-17636G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958701 | ||||||
| chr3:46958881
|
T | C | 1 | a0001c0001t0001g0303 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.96+17756A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46958881 | ||||||
| chr3:46959055
|
TA | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+17581delT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46959055 | ||||||
| chr3:46959116
|
T | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+17521A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46959116 | ||||||
| chr3:46959207
|
CA | C | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.96+17429delT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46959207 | ||||||
| chr3:46959414
|
G | C | 1 | a0001c0001t0001g0324 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.96+17223C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46959414 | ||||||
| chr3:46959457
|
T | C | 2 | a0002c0003t0001g0157a0002c0003t0001g0158 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.96+17180A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46959457 | ||||||
| chr3:46959540
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.96+17097G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46959540 | ||||||
| chr3:46959553
|
T | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+17084A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46959553 | ||||||
| chr3:46959594
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.96+17043G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46959594 | ||||||
| chr3:46959702
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.96+16935C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46959702 | ||||||
| chr3:46959860
|
C | T | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.96+16777G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46959860 | ||||||
| chr3:46960006
|
G | C | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.96+16631C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960006 | ||||||
| chr3:46960177
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.96+16460C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960177 | ||||||
| chr3:46960230
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.96+16407C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960230 | ||||||
| chr3:46960258
|
G | A | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.96+16379C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960258 | ||||||
| chr3:46960338
|
T | G | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.96+16299A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960338 | ||||||
| chr3:46960461
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.96+16176G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960461 | ||||||
| chr3:46960500
|
A | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+16137T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960500 | ||||||
| chr3:46960605
|
G | A | 1 | a0001c0002t0001g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.96+16032C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960605 | ||||||
| chr3:46960650
|
C | T | 13 | a0001c0001t0001g0167a0001c0001t0001g0266a0001c0001t0001g0267others(10): Show | 15 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+15987G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960650 | ||||||
| chr3:46960741
|
A | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+15896T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960741 | ||||||
| chr3:46960813
|
C | T | 2 | a0001c0001t0002g0039a0002c0003t0001g0149 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.96+15824G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960813 | ||||||
| chr3:46960903
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.96+15734C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46960903 | ||||||
| chr3:46961224
|
A | C | 1 | a0001c0001t0001g0056 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.96+15413T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961224 | ||||||
| chr3:46961352
|
T | C | 1 | a0001c0001t0002g0275 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.96+15285A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961352 | ||||||
| chr3:46961391
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+15246T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961391 | ||||||
| chr3:46961401
|
C | T | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.96+15236G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961401 | ||||||
| chr3:46961441
|
G | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+15196C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961441 | ||||||
| chr3:46961530
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+15107C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961530 | ||||||
| chr3:46961697
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.96+14940C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961697 | ||||||
| chr3:46961854
|
G | A | 329 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(326): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.96+14783C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961854 | ||||||
| chr3:46961894
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.96+14743A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961894 | ||||||
| chr3:46961905
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02132.hp1 NA18951.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.96+14732A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961905 | ||||||
| chr3:46961914
|
T | C | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.96+14723A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961914 | ||||||
| chr3:46961966
|
C | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.96+14671G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46961966 | ||||||
| chr3:46962048
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.96+14589A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962048 | ||||||
| chr3:46962121
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+14516C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962121 | ||||||
| chr3:46962153
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+14484C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962153 | ||||||
| chr3:46962164
|
C | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+14473G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962164 | ||||||
| chr3:46962170
|
T | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+14467A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962170 | ||||||
| chr3:46962215
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+14422A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962215 | ||||||
| chr3:46962331
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.96+14306C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962331 | ||||||
| chr3:46962395
|
T | C | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.96+14242A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962395 | ||||||
| chr3:46962412
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+14225A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962412 | ||||||
| chr3:46962426
|
C | A | 31 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0316others(28): Show | 31 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+14211G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962426 | ||||||
| chr3:46962434
|
C | CA | 10 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 10 | HG00738.hp1 HG01256.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+14202dupT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962434 | ||||||
| chr3:46962434
|
C | CAA | 73 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(70): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+14201_96+14202d others(4): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962434 | ||||||
| chr3:46962434
|
C | CAAA | 100 | a0001c0001t0001g0030a0001c0001t0001g0052a0001c0001t0001g0055others(97): Show | 100 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.96+14200_96+14202d others(5): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962434 | ||||||
| chr3:46962434
|
C | CAAAA | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(123): Show | 128 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.96+14199_96+14202d others(6): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962434 | ||||||
| chr3:46962434
|
C | CAAAAA | 14 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0028others(11): Show | 15 | HG00280.hp1 HG01106.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+14198_96+14202d others(7): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962434 | ||||||
| chr3:46962434
|
C | CAAAAAAA others(10): Show |
1 | a0001c0002t0001g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.96+14186_96+14202d others(19): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962434 | ||||||
| chr3:46962434
|
C | CAAAAAAA others(12): Show |
1 | a0001c0002t0001g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.96+14184_96+14202d others(21): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962434 | ||||||
| chr3:46962482
|
A | G | 329 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(326): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.96+14155T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962482 | ||||||
| chr3:46962539
|
A | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+14098T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962539 | ||||||
| chr3:46962687
|
G | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+13950C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962687 | ||||||
| chr3:46962783
|
T | C | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+13854A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962783 | ||||||
| chr3:46962828
|
T | C | 1 | a0001c0001t0002g0272 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.96+13809A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46962828 | ||||||
| chr3:46963038
|
T | G | 1 | a0001c0001t0001g0126 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.96+13599A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963038 | ||||||
| chr3:46963389
|
CTCTCCCT others(22): Show |
C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+13219_96+13247d others(31): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963389 | ||||||
| chr3:46963441
|
GTCTCCC | G | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.96+13190_96+13195d others(8): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963441 | ||||||
| chr3:46963508
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+13129G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963508 | ||||||
| chr3:46963581
|
G | A | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.96+13056C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963581 | ||||||
| chr3:46963646
|
C | T | 1 | a0003c0005t0001g0081 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.96+12991G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963646 | ||||||
| chr3:46963698
|
T | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.96+12939A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963698 | ||||||
| chr3:46963698
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+12939A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963698 | ||||||
| chr3:46963700
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.96+12937G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963700 | ||||||
| chr3:46963720
|
G | C | 1 | a0001c0001t0002g0175 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.96+12917C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963720 | ||||||
| chr3:46963726
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+12911C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963726 | ||||||
| chr3:46963773
|
G | C | 1 | a0001c0001t0002g0247 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.96+12864C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963773 | ||||||
| chr3:46963868
|
C | T | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.96+12769G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963868 | ||||||
| chr3:46963882
|
T | C | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.96+12755A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963882 | ||||||
| chr3:46963900
|
TCTCTGCC others(32): Show |
T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+12698_96+12736d others(41): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963900 | ||||||
| chr3:46963937
|
C | T | 1 | a0001c0001t0002g0248 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.96+12700G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46963937 | ||||||
| chr3:46964011
|
G | A | 3 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0322 | 3 | HG01934.hp1 HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.96+12626C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964011 | ||||||
| chr3:46964015
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.96+12622C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964015 | ||||||
| chr3:46964092
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.96+12545G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964092 | ||||||
| chr3:46964141
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.96+12496C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964141 | ||||||
| chr3:46964149
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+12488G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964149 | ||||||
| chr3:46964150
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.96+12487C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964150 | ||||||
| chr3:46964174
|
G | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+12463C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964174 | ||||||
| chr3:46964177
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+12460A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964177 | ||||||
| chr3:46964178
|
G | A | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.96+12459C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964178 | ||||||
| chr3:46964269
|
C | T | 2 | a0001c0001t0002g0165a0001c0001t0002g0190 | 2 | HG00639.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.96+12368G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964269 | ||||||
| chr3:46964320
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.96+12317C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964320 | ||||||
| chr3:46964357
|
C | T | 3 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0002g0189 | 3 | HG01934.hp1 HG02486.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.96+12280G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964357 | ||||||
| chr3:46964409
|
G | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG01070.hp1 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.96+12228C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964409 | ||||||
| chr3:46964491
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+12146G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964491 | ||||||
| chr3:46964519
|
GGTGGGGA others(7): Show |
G | 1 | a0001c0001t0001g0066 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.96+12104_96+12117d others(16): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964519 | ||||||
| chr3:46964676
|
G | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+11961C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964676 | ||||||
| chr3:46964742
|
G | A | 64 | a0001c0001t0002g0026a0001c0001t0002g0046a0001c0001t0002g0160others(61): Show | 64 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.96+11895C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964742 | ||||||
| chr3:46964812
|
T | C | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+11825A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964812 | ||||||
| chr3:46964815
|
T | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+11822A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964815 | ||||||
| chr3:46964818
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+11819T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964818 | ||||||
| chr3:46964856
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.96+11781A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46964856 | ||||||
| chr3:46965220
|
C | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0310a0001c0001t0001g0311 | 3 | HG01934.hp1 HG02486.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.96+11417G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46965220 | ||||||
| chr3:46965236
|
C | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+11401G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46965236 | ||||||
| chr3:46965394
|
T | C | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.96+11243A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46965394 | ||||||
| chr3:46965417
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.96+11220C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46965417 | ||||||
| chr3:46965765
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.96+10872A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46965765 | ||||||
| chr3:46965779
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.96+10858G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46965779 | ||||||
| chr3:46965798
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+10839G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46965798 | ||||||
| chr3:46965898
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.96+10739G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46965898 | ||||||
| chr3:46966191
|
T | C | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.96+10446A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966191 | ||||||
| chr3:46966374
|
G | A | 4 | a0001c0002t0001g0015a0001c0002t0001g0020a0001c0002t0001g0021others(1): Show | 4 | HG02723.hp1 HG02886.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+10263C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966374 | ||||||
| chr3:46966375
|
C | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.96+10262G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966375 | ||||||
| chr3:46966490
|
T | G | 1 | a0001c0001t0001g0056 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.96+10147A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966490 | ||||||
| chr3:46966523
|
A | C | 138 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(135): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.96+10114T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966523 | ||||||
| chr3:46966523
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+10114T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966523 | ||||||
| chr3:46966542
|
A | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+10095T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966542 | ||||||
| chr3:46966597
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+10040A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966597 | ||||||
| chr3:46966606
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+10031C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966606 | ||||||
| chr3:46966668
|
A | C | 327 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.96+9969T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966668 | ||||||
| chr3:46966671
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0131others(2): Show | 6 | NA18944.hp2 NA18954.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+9966C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966671 | ||||||
| chr3:46966746
|
CTTAATTT others(11): Show |
C | 2 | a0001c0001t0002g0164a0001c0001t0002g0188 | 2 | NA18949.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.96+9873_96+9890del others(18): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966746 | ||||||
| chr3:46966765
|
T | G | 341 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(338): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.96+9872A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966765 | ||||||
| chr3:46966803
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+9834A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966803 | ||||||
| chr3:46966922
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+9715C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966922 | ||||||
| chr3:46966961
|
T | A | 1 | a0001c0001t0002g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.96+9676A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46966961 | ||||||
| chr3:46967081
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.96+9556A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46967081 | ||||||
| chr3:46967116
|
C | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.96+9521G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46967116 | ||||||
| chr3:46967248
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0076 | 2 | HG01106.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.96+9389C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46967248 | ||||||
| chr3:46967407
|
C | T | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.96+9230G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46967407 | ||||||
| chr3:46967559
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+9078T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46967559 | ||||||
| chr3:46967599
|
A | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+9038T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46967599 | ||||||
| chr3:46967727
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+8910A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46967727 | ||||||
| chr3:46967792
|
T | C | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.96+8845A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46967792 | ||||||
| chr3:46967938
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+8699G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46967938 | ||||||
| chr3:46968061
|
T | C | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+8576A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968061 | ||||||
| chr3:46968246
|
T | C | 1 | a0001c0001t0002g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.96+8391A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968246 | ||||||
| chr3:46968268
|
T | G | 6 | a0001c0001t0001g0326a0001c0001t0001g0329a0001c0001t0001g0341others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+8369A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968268 | ||||||
| chr3:46968315
|
C | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+8322G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968315 | ||||||
| chr3:46968355
|
C | CG | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+8281dupC | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968355 | ||||||
| chr3:46968425
|
A | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.96+8212T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968425 | ||||||
| chr3:46968550
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.96+8087A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968550 | ||||||
| chr3:46968554
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.96+8083C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968554 | ||||||
| chr3:46968621
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.96+8016A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968621 | ||||||
| chr3:46968626
|
C | A | 1 | a0001c0001t0002g0276 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.96+8011G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968626 | ||||||
| chr3:46968803
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.96+7834T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968803 | ||||||
| chr3:46968837
|
C | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+7800G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46968837 | ||||||
| chr3:46969000
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+7637G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969000 | ||||||
| chr3:46969001
|
G | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+7636C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969001 | ||||||
| chr3:46969152
|
C | A | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.96+7485G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969152 | ||||||
| chr3:46969622
|
C | T | 14 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0006others(11): Show | 15 | HG01255.hp2 HG01358.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+7015G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969622 | ||||||
| chr3:46969630
|
G | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+7007C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969630 | ||||||
| chr3:46969711
|
T | C | 1 | a0001c0001t0002g0276 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.96+6926A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969711 | ||||||
| chr3:46969740
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.96+6897C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969740 | ||||||
| chr3:46969742
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.96+6895C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969742 | ||||||
| chr3:46969820
|
C | T | 1 | a0001c0001t0002g0276 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.96+6817G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969820 | ||||||
| chr3:46969869
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.96+6768T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969869 | ||||||
| chr3:46969901
|
CT | C | 21 | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0050others(18): Show | 21 | HG01891.hp1 HG01934.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+6735delA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969901 | ||||||
| chr3:46969901
|
CTT | C | 301 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(298): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.96+6734_96+6735del others(2): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969901 | ||||||
| chr3:46969940
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+6697A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969940 | ||||||
| chr3:46969945
|
C | T | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.96+6692G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46969945 | ||||||
| chr3:46970018
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+6619C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970018 | ||||||
| chr3:46970087
|
G | T | 1 | a0001c0001t0002g0172 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.96+6550C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970087 | ||||||
| chr3:46970094
|
T | C | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+6543A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970094 | ||||||
| chr3:46970280
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.96+6357A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970280 | ||||||
| chr3:46970284
|
A | AT | 73 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0306others(70): Show | 73 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.96+6352dupA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970284 | ||||||
| chr3:46970284
|
A | ATT | 251 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.96+6351_96+6352dup others(2): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970284 | ||||||
| chr3:46970325
|
C | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+6312G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970325 | ||||||
| chr3:46970379
|
G | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+6258C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970379 | ||||||
| chr3:46970475
|
A | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+6162T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970475 | ||||||
| chr3:46970660
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.96+5977C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970660 | ||||||
| chr3:46970689
|
T | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+5948A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970689 | ||||||
| chr3:46970703
|
T | C | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+5934A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970703 | ||||||
| chr3:46970822
|
AAG | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+5813_96+5814del others(2): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970822 | ||||||
| chr3:46970876
|
G | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+5761C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970876 | ||||||
| chr3:46970878
|
C | A | 1 | a0001c0001t0002g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.96+5759G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970878 | ||||||
| chr3:46970893
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.96+5744C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46970893 | ||||||
| chr3:46971114
|
C | G | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.96+5523G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971114 | ||||||
| chr3:46971129
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+5508C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971129 | ||||||
| chr3:46971137
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+5500G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971137 | ||||||
| chr3:46971154
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.96+5483G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971154 | ||||||
| chr3:46971255
|
T | C | 1 | a0002c0003t0001g0135 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.96+5382A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971255 | ||||||
| chr3:46971282
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.96+5355C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971282 | ||||||
| chr3:46971289
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.96+5348G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971289 | ||||||
| chr3:46971450
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+5187G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971450 | ||||||
| chr3:46971486
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.96+5151A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971486 | ||||||
| chr3:46971491
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+5146T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971491 | ||||||
| chr3:46971553
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.96+5084C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971553 | ||||||
| chr3:46971640
|
TTA | T | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.96+4995_96+4996del others(2): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971640 | ||||||
| chr3:46971729
|
T | C | 13 | a0001c0001t0001g0167a0001c0001t0001g0266a0001c0001t0001g0267others(10): Show | 15 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+4908A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971729 | ||||||
| chr3:46971737
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+4900C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971737 | ||||||
| chr3:46971748
|
A | T | 1 | a0001c0001t0002g0231 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.96+4889T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971748 | ||||||
| chr3:46971792
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.96+4845A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971792 | ||||||
| chr3:46971856
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.96+4781A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971856 | ||||||
| chr3:46971959
|
A | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+4678T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971959 | ||||||
| chr3:46971962
|
A | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+4675T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971962 | ||||||
| chr3:46971976
|
A | G | 1 | a0001c0001t0002g0275 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.96+4661T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971976 | ||||||
| chr3:46971982
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.96+4655G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46971982 | ||||||
| chr3:46972052
|
T | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+4585A>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972052 | ||||||
| chr3:46972062
|
T | TA | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.96+4574dupT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972062 | ||||||
| chr3:46972137
|
A | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0076 | 2 | HG01106.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.96+4500T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972137 | ||||||
| chr3:46972168
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.96+4469G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972168 | ||||||
| chr3:46972179
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.96+4458T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972179 | ||||||
| chr3:46972239
|
C | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+4398G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972239 | ||||||
| chr3:46972240
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+4397T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972240 | ||||||
| chr3:46972321
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+4316A>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972321 | ||||||
| chr3:46972426
|
A | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(7): Show | 11 | HG00738.hp2 HG01074.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.96+4211T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972426 | ||||||
| chr3:46972457
|
A | C | 1 | a0001c0001t0002g0180 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.96+4180T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972457 | ||||||
| chr3:46972773
|
T | TA | 151 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(148): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.96+3863dupT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972773 | ||||||
| chr3:46972773
|
T | TAA | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.96+3862_96+3863dup others(2): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972773 | ||||||
| chr3:46972783
|
A | AG | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.96+3853_96+3854ins others(1): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972783 | ||||||
| chr3:46972911
|
A | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+3726T>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972911 | ||||||
| chr3:46972974
|
G | A | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.96+3663C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46972974 | ||||||
| chr3:46973050
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+3587G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973050 | ||||||
| chr3:46973053
|
G | A | 1 | a0001c0001t0002g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+3584C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973053 | ||||||
| chr3:46973198
|
A | AT | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(321): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.96+3438_96+3439ins others(1): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973198 | ||||||
| chr3:46973254
|
A | G | 329 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(326): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.96+3383T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973254 | ||||||
| chr3:46973308
|
G | A | 59 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(56): Show | 62 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.96+3329C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973308 | ||||||
| chr3:46973316
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.96+3321C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973316 | ||||||
| chr3:46973321
|
C | G | 1 | a0001c0001t0001g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.96+3316G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973321 | ||||||
| chr3:46973337
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.96+3300C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973337 | ||||||
| chr3:46973344
|
GCTCCATC others(135): Show |
G | 5 | a0001c0001t0001g0316a0001c0001t0001g0320a0001c0001t0001g0321others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+3151_96+3292del | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973344 | ||||||
| chr3:46973353
|
C | CA | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.96+3283dupT | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973353 | ||||||
| chr3:46973353
|
C | CAA | 38 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0049others(35): Show | 38 | HG00609.hp2 HG00673.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.96+3282_96+3283dup others(2): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973353 | ||||||
| chr3:46973458
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+3179C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973458 | ||||||
| chr3:46973458
|
G | T | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.96+3179C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973458 | ||||||
| chr3:46973459
|
C | T | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0167others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.96+3178G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973459 | ||||||
| chr3:46973613
|
CT | C | 144 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0048others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.96+3023delA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973613 | ||||||
| chr3:46973613
|
CTT | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.96+3022_96+3023del others(2): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973613 | ||||||
| chr3:46973618
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+3019A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973618 | ||||||
| chr3:46973653
|
G | A | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.96+2984C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973653 | ||||||
| chr3:46973706
|
A | G | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.96+2931T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973706 | ||||||
| chr3:46973709
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.96+2928A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973709 | ||||||
| chr3:46973815
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+2822A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973815 | ||||||
| chr3:46973936
|
G | A | 1 | a0001c0001t0002g0283 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.96+2701C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973936 | ||||||
| chr3:46973998
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.96+2639C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46973998 | ||||||
| chr3:46974065
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+2572T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46974065 | ||||||
| chr3:46974140
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.96+2497T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46974140 | ||||||
| chr3:46974401
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.96+2236C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46974401 | ||||||
| chr3:46974455
|
C | T | 17 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(14): Show | 17 | HG00099.hp1 HG00597.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.96+2182G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46974455 | ||||||
| chr3:46974569
|
G | GCTAA | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+2067_96+2068ins others(4): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46974569 | ||||||
| chr3:46974651
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.96+1986G>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46974651 | ||||||
| chr3:46974682
|
G | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+1955C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46974682 | ||||||
| chr3:46974727
|
G | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+1910C>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46974727 | ||||||
| chr3:46975190
|
A | AT | 6 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0056others(3): Show | 6 | HG00741.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+1446dupA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975190 | ||||||
| chr3:46975190
|
AT | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0344others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+1446delA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975190 | ||||||
| chr3:46975279
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.96+1358T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975279 | ||||||
| chr3:46975425
|
C | T | 32 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(29): Show | 32 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.96+1212G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975425 | ||||||
| chr3:46975526
|
CT | C | 19 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 19 | HG00597.hp1 HG01169.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+1110delA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975526 | ||||||
| chr3:46975526
|
CTT | C | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.96+1109_96+1110del others(2): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975526 | ||||||
| chr3:46975526
|
CTTT | C | 13 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0155others(10): Show | 13 | HG01257.hp1 HG01943.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.96+1108_96+1110del others(3): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975526 | ||||||
| chr3:46975526
|
CTTTTTTT others(4): Show |
C | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.96+1100_96+1110del others(11): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975526 | ||||||
| chr3:46975526
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0156 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.96+1099_96+1110del others(12): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975526 | ||||||
| chr3:46975678
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+959G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975678 | ||||||
| chr3:46975692
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.96+945C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975692 | ||||||
| chr3:46975765
|
T | C | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.96+872A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975765 | ||||||
| chr3:46975815
|
G | C | 2 | a0002c0003t0001g0157a0002c0003t0001g0158 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.96+822C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975815 | ||||||
| chr3:46975839
|
C | T | 1 | a0001c0001t0002g0172 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.96+798G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975839 | ||||||
| chr3:46975841
|
AT | A | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.96+795delA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975841 | ||||||
| chr3:46975841
|
ATT | A | 18 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(15): Show | 18 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.96+794_96+795delAA | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975841 | ||||||
| chr3:46975841
|
ATTT | A | 124 | a0001c0001t0001g0173a0001c0001t0001g0230a0001c0001t0001g0232others(121): Show | 127 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.96+793_96+795delAA others(1): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975841 | ||||||
| chr3:46975841
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0002g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.96+786_96+795delAA others(8): Show |
CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46975841 | ||||||
| chr3:46976164
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01884.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.96+473C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976164 | ||||||
| chr3:46976193
|
G | A | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(317): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.96+444C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976193 | ||||||
| chr3:46976217
|
G | C | 21 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+420C>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976217 | ||||||
| chr3:46976405
|
T | C | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+232A>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976405 | ||||||
| chr3:46976425
|
A | G | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.96+212T>C | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976425 | ||||||
| chr3:46976433
|
C | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.96+204G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976433 | ||||||
| chr3:46976510
|
C | A | 1 | a0001c0001t0002g0312 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.96+127G>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976510 | ||||||
| chr3:46976523
|
G | A | 1 | a0001c0001t0002g0313 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.96+114C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976523 | ||||||
| chr3:46976565
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.96+72C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976565 | ||||||
| chr3:46976580
|
G | A | 29 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(26): Show | 29 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.96+57C>T | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976580 | ||||||
| chr3:46976587
|
A | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02132.hp1 NA18951.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.96+50T>G | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976587 | ||||||
| chr3:46976602
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.96+35G>A | CCDC12 | ENSG00000160799.12 | transcript | ENST00000683445.1 | protein_coding | 1/6 | chr3 | 46976602 |