Search by Gene
| geneid | 728591 |
|---|---|
| ensemblid | ENSG00000242715.8 |
| hgncid | 34361 |
| symbol | CCDC169 |
| name | coiled-coil domain containing 169 |
| refseq_nuc | NM_001144981.3 |
| refseq_prot | NP_001138453.1 |
| ensembl_nuc | ENST00000239859.8 |
| ensembl_prot | ENSP00000239859.7 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 36230775 |
| end | 36297814 |
| strand | - |
| ver | v1.2 |
| region | chr13:36230775-36297814 |
| region5000 | chr13:36225775-36302814 |
| regionname0 | CCDC169_chr13_36230775_36297814 |
| regionname5000 | CCDC169_chr13_36225775_36302814 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 214 | 240 | 65 | 36 | 108 | 8 | 21 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0002 | 0/0 | 214 | 121 | 18 | 26 | 50 | 6 | 21 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0003 | 0/0 | 214 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0004 | 0/0 | 214 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 645 | 208 | 57 | 32 | 89 | 8 | 20 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| c0002 | 0/0 | 645 | 86 | 8 | 16 | 46 | 4 | 12 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| c0003 | 0/0 | 645 | 35 | 10 | 10 | 4 | 2 | 9 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| c0004 | 0/0 | 645 | 23 | 1 | 3 | 18 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| c0005 | 0/0 | 645 | 8 | 7 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| c0006 | 0/0 | 645 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| c0007 | 0/0 | 645 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| c0008 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 514 | 239 | 64 | 36 | 108 | 8 | 21 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| t0002 | 0/0 | 513 | 117 | 15 | 26 | 49 | 6 | 21 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| t0003 | 0/0 | 514 | 7 | 6 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| t0004 | 0/0 | 514 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0002 | 0/0 | 6 | 4 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0005 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0006 | 0/0 | 5 | 0 | 0 | 1 | 2 | 2 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0007 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0018 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 208 | 57 | 32 | 89 | 8 | 20 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 23 | 1 | 3 | 18 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0001c0007 | a0001 | c0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 86 | 8 | 16 | 46 | 4 | 12 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 35 | 10 | 10 | 4 | 2 | 9 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0003c0006 | a0003 | c0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0004c0008 | a0004 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 207 | 56 | 32 | 89 | 8 | 20 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 23 | 1 | 3 | 18 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0001c0007t0001 | a0001 | c0007 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0002c0002t0002 | a0002 | c0002 | t0002 | 0/0 | 83 | 6 | 16 | 45 | 4 | 12 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0002c0002t0003 | a0002 | c0002 | t0003 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0002c0003t0002 | a0002 | c0003 | t0002 | 0/0 | 32 | 7 | 10 | 4 | 2 | 9 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0002c0003t0003 | a0002 | c0003 | t0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0003c0006t0002 | a0003 | c0006 | t0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| a0004c0008t0003 | a0004 | c0008 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 6 | 4 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0001t0004g0104 | a0001 | c0001 | t0004 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0009 | a0001 | c0004 | t0001 | g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0015 | a0001 | c0004 | t0001 | g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0035 | a0001 | c0004 | t0001 | g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0221 | a0001 | c0004 | t0001 | g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0225 | a0001 | c0004 | t0001 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0237 | a0001 | c0004 | t0001 | g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0240 | a0001 | c0004 | t0001 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0258 | a0001 | c0004 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0259 | a0001 | c0004 | t0001 | g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0264 | a0001 | c0004 | t0001 | g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0265 | a0001 | c0004 | t0001 | g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0266 | a0001 | c0004 | t0001 | g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0274 | a0001 | c0004 | t0001 | g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0276 | a0001 | c0004 | t0001 | g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0280 | a0001 | c0004 | t0001 | g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0285 | a0001 | c0004 | t0001 | g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0004t0001g0293 | a0001 | c0004 | t0001 | g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0005t0001g0058 | a0001 | c0005 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0005t0001g0059 | a0001 | c0005 | t0001 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0005t0001g0060 | a0001 | c0005 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0005t0001g0061 | a0001 | c0005 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0005t0001g0062 | a0001 | c0005 | t0001 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0005t0001g0063 | a0001 | c0005 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0005t0001g0064 | a0001 | c0005 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0005t0001g0065 | a0001 | c0005 | t0001 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0001c0007t0001g0068 | a0001 | c0007 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0003 | a0002 | c0002 | t0002 | g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0006 | a0002 | c0002 | t0002 | g0006 | 0/0 | 5 | 0 | 0 | 1 | 2 | 2 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0030 | a0002 | c0002 | t0002 | g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0031 | a0002 | c0002 | t0002 | g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0032 | a0002 | c0002 | t0002 | g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0033 | a0002 | c0002 | t0002 | g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0034 | a0002 | c0002 | t0002 | g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0036 | a0002 | c0002 | t0002 | g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0188 | a0002 | c0002 | t0002 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0218 | a0002 | c0002 | t0002 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0219 | a0002 | c0002 | t0002 | g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0220 | a0002 | c0002 | t0002 | g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0222 | a0002 | c0002 | t0002 | g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0223 | a0002 | c0002 | t0002 | g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0224 | a0002 | c0002 | t0002 | g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0226 | a0002 | c0002 | t0002 | g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0227 | a0002 | c0002 | t0002 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0228 | a0002 | c0002 | t0002 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0229 | a0002 | c0002 | t0002 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0230 | a0002 | c0002 | t0002 | g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0231 | a0002 | c0002 | t0002 | g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0232 | a0002 | c0002 | t0002 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0233 | a0002 | c0002 | t0002 | g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0234 | a0002 | c0002 | t0002 | g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0235 | a0002 | c0002 | t0002 | g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0236 | a0002 | c0002 | t0002 | g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0238 | a0002 | c0002 | t0002 | g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0239 | a0002 | c0002 | t0002 | g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0241 | a0002 | c0002 | t0002 | g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0242 | a0002 | c0002 | t0002 | g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0243 | a0002 | c0002 | t0002 | g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0244 | a0002 | c0002 | t0002 | g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0245 | a0002 | c0002 | t0002 | g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0246 | a0002 | c0002 | t0002 | g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0247 | a0002 | c0002 | t0002 | g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0248 | a0002 | c0002 | t0002 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0250 | a0002 | c0002 | t0002 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0251 | a0002 | c0002 | t0002 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0252 | a0002 | c0002 | t0002 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0253 | a0002 | c0002 | t0002 | g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0254 | a0002 | c0002 | t0002 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0255 | a0002 | c0002 | t0002 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0256 | a0002 | c0002 | t0002 | g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0257 | a0002 | c0002 | t0002 | g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0260 | a0002 | c0002 | t0002 | g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0261 | a0002 | c0002 | t0002 | g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0262 | a0002 | c0002 | t0002 | g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0263 | a0002 | c0002 | t0002 | g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0267 | a0002 | c0002 | t0002 | g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0268 | a0002 | c0002 | t0002 | g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0269 | a0002 | c0002 | t0002 | g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0270 | a0002 | c0002 | t0002 | g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0271 | a0002 | c0002 | t0002 | g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0272 | a0002 | c0002 | t0002 | g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0273 | a0002 | c0002 | t0002 | g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0275 | a0002 | c0002 | t0002 | g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0277 | a0002 | c0002 | t0002 | g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0278 | a0002 | c0002 | t0002 | g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0279 | a0002 | c0002 | t0002 | g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0281 | a0002 | c0002 | t0002 | g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0282 | a0002 | c0002 | t0002 | g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0283 | a0002 | c0002 | t0002 | g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0284 | a0002 | c0002 | t0002 | g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0286 | a0002 | c0002 | t0002 | g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0287 | a0002 | c0002 | t0002 | g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0290 | a0002 | c0002 | t0002 | g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0291 | a0002 | c0002 | t0002 | g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0002g0292 | a0002 | c0002 | t0002 | g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0003g0217 | a0002 | c0002 | t0003 | g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0003g0249 | a0002 | c0002 | t0003 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0002t0003g0289 | a0002 | c0002 | t0003 | g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0016 | a0002 | c0003 | t0002 | g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0017 | a0002 | c0003 | t0002 | g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0018 | a0002 | c0003 | t0002 | g0018 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0037 | a0002 | c0003 | t0002 | g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0038 | a0002 | c0003 | t0002 | g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0039 | a0002 | c0003 | t0002 | g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0040 | a0002 | c0003 | t0002 | g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0041 | a0002 | c0003 | t0002 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0042 | a0002 | c0003 | t0002 | g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0043 | a0002 | c0003 | t0002 | g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0044 | a0002 | c0003 | t0002 | g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0045 | a0002 | c0003 | t0002 | g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0047 | a0002 | c0003 | t0002 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0048 | a0002 | c0003 | t0002 | g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0051 | a0002 | c0003 | t0002 | g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0052 | a0002 | c0003 | t0002 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0053 | a0002 | c0003 | t0002 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0054 | a0002 | c0003 | t0002 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0055 | a0002 | c0003 | t0002 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0075 | a0002 | c0003 | t0002 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0144 | a0002 | c0003 | t0002 | g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0164 | a0002 | c0003 | t0002 | g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0174 | a0002 | c0003 | t0002 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0175 | a0002 | c0003 | t0002 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0176 | a0002 | c0003 | t0002 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0185 | a0002 | c0003 | t0002 | g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0186 | a0002 | c0003 | t0002 | g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0187 | a0002 | c0003 | t0002 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0002g0190 | a0002 | c0003 | t0002 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0002c0003t0003g0010 | a0002 | c0003 | t0003 | g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0003c0006t0002g0049 | a0003 | c0006 | t0002 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0003c0006t0002g0050 | a0003 | c0006 | t0002 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| a0004c0008t0003g0288 | a0004 | c0008 | t0003 | g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0245 | EUR | GBR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0018 | EUR | GBR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0226 | EUR | GBR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00280 | hp1 | a0002 | c0003 | t0002 | g0042 | EUR | FIN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | FIN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00423 | hp2 | a0002 | c0003 | t0002 | g0175 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00621 | hp1 | a0002 | c0003 | t0002 | g0174 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00639 | hp1 | a0002 | c0003 | t0002 | g0047 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0277 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0272 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00733 | hp1 | a0002 | c0003 | t0002 | g0048 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0275 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00738 | hp1 | a0002 | c0003 | t0002 | g0045 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0278 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01069 | hp2 | a0002 | c0003 | t0002 | g0017 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0044 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0283 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01106 | hp2 | a0001 | c0005 | t0001 | g0062 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01167 | hp2 | a0002 | c0003 | t0002 | g0051 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01169 | hp2 | a0002 | c0003 | t0002 | g0040 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01175 | hp1 | a0002 | c0003 | t0002 | g0052 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0243 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0257 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0282 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0043 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0253 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | IBS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01981 | hp1 | a0001 | c0004 | t0001 | g0264 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0030 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01993 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01993 | hp2 | a0002 | c0003 | t0002 | g0144 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0235 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0015 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0234 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0247 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0240 | EAS | CDX | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | CDX | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02257 | hp1 | a0002 | c0002 | t0003 | g0289 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02257 | hp2 | a0003 | c0006 | t0002 | g0050 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02280 | hp1 | a0002 | c0002 | t0003 | g0217 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02300 | hp1 | a0001 | c0004 | t0001 | g0221 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02523 | hp1 | a0002 | c0003 | t0002 | g0190 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02602 | hp2 | a0002 | c0003 | t0002 | g0038 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0220 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0061 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0222 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0059 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02683 | hp1 | a0002 | c0003 | t0002 | g0039 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02723 | hp2 | a0004 | c0008 | t0003 | g0288 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0224 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0273 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02738 | hp2 | a0001 | c0004 | t0001 | g0274 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0244 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02896 | hp1 | a0002 | c0003 | t0002 | g0053 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02897 | hp2 | a0002 | c0003 | t0002 | g0054 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0293 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02976 | hp2 | a0001 | c0005 | t0001 | g0065 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03041 | hp2 | a0002 | c0003 | t0002 | g0187 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0219 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0063 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03130 | hp1 | a0002 | c0003 | t0003 | g0010 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03139 | hp2 | a0002 | c0003 | t0002 | g0055 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0060 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0261 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03669 | hp1 | a0002 | c0003 | t0002 | g0075 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03669 | hp2 | a0002 | c0003 | t0002 | g0037 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0223 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03704 | hp1 | a0002 | c0003 | t0002 | g0164 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03704 | hp2 | a0002 | c0003 | t0002 | g0016 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03834 | hp2 | a0002 | c0003 | t0002 | g0185 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0262 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG04115 | hp1 | a0002 | c0003 | t0002 | g0017 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0242 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0016 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18612 | hp1 | a0001 | c0004 | t0001 | g0265 | EAS | CHB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0058 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0237 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18946 | hp2 | a0001 | c0004 | t0001 | g0266 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18954 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18971 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18981 | hp2 | a0001 | c0007 | t0001 | g0068 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18982 | hp2 | a0001 | c0004 | t0001 | g0035 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0276 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18988 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18989 | hp1 | a0001 | c0004 | t0001 | g0035 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18999 | hp1 | a0001 | c0004 | t0001 | g0285 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19002 | hp1 | a0001 | c0004 | t0001 | g0258 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0064 | AFR | LWK | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19057 | hp2 | a0002 | c0003 | t0002 | g0176 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0225 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19067 | hp1 | a0001 | c0004 | t0001 | g0259 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19085 | hp2 | a0001 | c0004 | t0001 | g0280 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19086 | hp2 | a0002 | c0002 | t0003 | g0249 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0232 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ASW | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | TSI | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | GIH | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0263 | SAS | GIH | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0279 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG02559 | hp2 | a0003 | c0006 | t0002 | g0049 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03471 | hp1 | a0002 | c0003 | t0002 | g0186 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG03471 | hp2 | a0002 | c0003 | t0003 | g0010 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | USA | CCDC169_chr13_36225775_36302814 | CCDC169 |
| HG06807 | hp2 | a0002 | c0003 | t0002 | g0041 | AFR | USA | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA20300 | hp1 | a0002 | c0003 | t0003 | g0010 | AFR | USA | CCDC169_chr13_36225775_36302814 | CCDC169 |
| NA20300 | hp2 | a0002 | c0003 | t0002 | g0018 | AFR | USA | CCDC169_chr13_36225775_36302814 | CCDC169 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0057 | REF | REF | CCDC169_chr13_36225775_36302814 | CCDC169 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0134 | REF | REF | CCDC169_chr13_36225775_36302814 | CCDC169 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:36230776
|
G | A | 1 | a0001 | 1 | HG03540.hp1 | splice_region_variant | LOW | c.*417C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 8/8 | chr13 | 36230776 | ||||||
| chr13:36248606
|
G | A | 1 | a0003 | 2 | HG02257.hp2 HG02559.hp2 |
missense_variant&splice_region_variant | MODERATE | c.545C>T | p.Thr182Ile | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/8 | 640/1158 | 545/645 | 182/214 | chr13 | 36248606 | ||
| chr13:36254100
|
T | C | 3 | a0002a0003a0004 | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
missense_variant | MODERATE | c.359A>G | p.Lys120Arg | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 5/8 | 454/1158 | 359/645 | 120/214 | chr13 | 36254100 | ||
| chr13:36283606
|
T | C | 1 | a0004 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.260A>G | p.His87Arg | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 3/8 | 355/1158 | 260/645 | 87/214 | chr13 | 36283606 | ||
| chr13:36295824
|
T | G | 1 | a0004 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.117A>C | p.Arg39Ser | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/8 | 212/1158 | 117/645 | 39/214 | chr13 | 36295824 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:36253820
|
G | A | 1 | a0001c0005 | 8 | HG01106.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.451C>T | p.Leu151Leu | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/8 | 546/1158 | 451/645 | 151/214 | chr13 | 36253820 | ||
| chr13:36254126
|
T | C | 1 | a0001c0007 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.333A>G | p.Leu111Leu | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 5/8 | 428/1158 | 333/645 | 111/214 | chr13 | 36254126 | ||
| chr13:36283502
|
T | C | 3 | a0001c0004a0002c0002a0004c0008 | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
synonymous_variant | LOW | c.282A>G | p.Leu94Leu | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/8 | 377/1158 | 282/645 | 94/214 | chr13 | 36283502 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:36231029
|
T | C | 6 | a0002c0002t0002a0002c0002t0003a0002c0003t0002others(3): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*164A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 8/8 | 164 | chr13 | 36231029 | |||||
| chr13:36231152
|
GA | G | 3 | a0002c0002t0002a0002c0003t0002a0003c0006t0002 | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*40delT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 8/8 | 40 | chr13 | 36231152 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:36231325
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.546-33T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231325 | ||||||
| chr13:36231392
|
C | T | 1 | a0002c0003t0002g0075 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.546-100G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231392 | ||||||
| chr13:36231409
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.546-117G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231409 | ||||||
| chr13:36231412
|
G | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(41): Show | 53 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.546-120C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231412 | ||||||
| chr13:36231488
|
C | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-196G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231488 | ||||||
| chr13:36231488
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.546-196G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231488 | ||||||
| chr13:36231512
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.546-220C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231512 | ||||||
| chr13:36231570
|
T | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-278A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231570 | ||||||
| chr13:36231645
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-353A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231645 | ||||||
| chr13:36231652
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-360G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231652 | ||||||
| chr13:36231697
|
G | A | 100 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(97): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.546-405C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231697 | ||||||
| chr13:36231833
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.546-541A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231833 | ||||||
| chr13:36231853
|
C | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-561G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231853 | ||||||
| chr13:36231876
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-584C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231876 | ||||||
| chr13:36231932
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.546-640G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36231932 | ||||||
| chr13:36232194
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.546-902C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36232194 | ||||||
| chr13:36232633
|
TAAGAATA others(84): Show |
T | 103 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(100): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.546-1432_546-1342d others(93): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36232633 | ||||||
| chr13:36232642
|
AAAAAAAG others(83): Show |
A | 1 | a0002c0002t0002g0286 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.546-1440_546-1351d others(92): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36232642 | ||||||
| chr13:36232913
|
T | C | 5 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.546-1621A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36232913 | ||||||
| chr13:36233099
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.546-1807C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233099 | ||||||
| chr13:36233226
|
GACT | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-1937_546-1935d others(5): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233226 | ||||||
| chr13:36233231
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-1939G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233231 | ||||||
| chr13:36233233
|
GTGTC | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-1945_546-1942d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233233 | ||||||
| chr13:36233286
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.546-1994G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233286 | ||||||
| chr13:36233299
|
A | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-2007T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233299 | ||||||
| chr13:36233379
|
C | T | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.546-2087G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233379 | ||||||
| chr13:36233395
|
C | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-2103G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233395 | ||||||
| chr13:36233408
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0191a0001c0001t0001g0197 | 5 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-2116A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233408 | ||||||
| chr13:36233518
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-2226A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233518 | ||||||
| chr13:36233522
|
A | ACTTTAAA others(3): Show |
5 | a0002c0002t0002g0286a0002c0002t0002g0287a0002c0003t0002g0174others(2): Show | 5 | HG00423.hp2 HG00621.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.546-2231_546-2230i others(12): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233522 | ||||||
| chr13:36233523
|
T | G | 5 | a0002c0002t0002g0286a0002c0002t0002g0287a0002c0003t0002g0174others(2): Show | 5 | HG00423.hp2 HG00621.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.546-2231A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233523 | ||||||
| chr13:36233523
|
T | TTTTAAAT others(3): Show |
99 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(96): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.546-2232_546-2231i others(12): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233523 | ||||||
| chr13:36233630
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546-2338A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233630 | ||||||
| chr13:36233692
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 52 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.546-2400C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233692 | ||||||
| chr13:36233812
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.546-2520A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233812 | ||||||
| chr13:36233902
|
T | C | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.546-2610A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233902 | ||||||
| chr13:36233929
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-2637T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36233929 | ||||||
| chr13:36234061
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 52 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.546-2769G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234061 | ||||||
| chr13:36234071
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.546-2779G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234071 | ||||||
| chr13:36234117
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-2825T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234117 | ||||||
| chr13:36234293
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-3001G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234293 | ||||||
| chr13:36234307
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-3015G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234307 | ||||||
| chr13:36234416
|
A | G | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.546-3124T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234416 | ||||||
| chr13:36234441
|
C | T | 1 | a0002c0002t0002g0262 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.546-3149G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234441 | ||||||
| chr13:36234532
|
A | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-3240T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234532 | ||||||
| chr13:36234536
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.546-3244G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234536 | ||||||
| chr13:36234682
|
G | A | 2 | a0002c0003t0003g0010a0004c0008t0003g0288 | 4 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-3390C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234682 | ||||||
| chr13:36234808
|
G | A | 2 | a0002c0003t0003g0010a0004c0008t0003g0288 | 4 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-3516C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234808 | ||||||
| chr13:36234853
|
C | T | 3 | a0002c0002t0002g0223a0002c0002t0002g0224a0002c0003t0002g0075 | 3 | HG02735.hp2 HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.546-3561G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36234853 | ||||||
| chr13:36235238
|
A | G | 2 | a0002c0003t0003g0010a0004c0008t0003g0288 | 4 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-3946T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36235238 | ||||||
| chr13:36235453
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-4161C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36235453 | ||||||
| chr13:36235664
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-4372T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36235664 | ||||||
| chr13:36235735
|
A | G | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.546-4443T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36235735 | ||||||
| chr13:36235748
|
T | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-4456A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36235748 | ||||||
| chr13:36235767
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.546-4475G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36235767 | ||||||
| chr13:36235784
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.546-4492C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36235784 | ||||||
| chr13:36235838
|
CTG | C | 62 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(59): Show | 77 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.546-4548_546-4547d others(4): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36235838 | ||||||
| chr13:36235947
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-4655C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36235947 | ||||||
| chr13:36236384
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.546-5092T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36236384 | ||||||
| chr13:36236462
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-5170G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36236462 | ||||||
| chr13:36236538
|
A | T | 100 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(97): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.546-5246T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36236538 | ||||||
| chr13:36236623
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.546-5331A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36236623 | ||||||
| chr13:36236646
|
T | C | 1 | a0001c0001t0001g0026 | 2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.546-5354A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36236646 | ||||||
| chr13:36236891
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.546-5599C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36236891 | ||||||
| chr13:36236915
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-5623G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36236915 | ||||||
| chr13:36236931
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-5639G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36236931 | ||||||
| chr13:36236980
|
TTAACA | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-5693_546-5689d others(7): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36236980 | ||||||
| chr13:36237003
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-5711T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237003 | ||||||
| chr13:36237017
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-5725A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237017 | ||||||
| chr13:36237069
|
GTATTAT | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-5783_546-5778d others(8): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237069 | ||||||
| chr13:36237266
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-5974C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237266 | ||||||
| chr13:36237389
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.546-6097G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237389 | ||||||
| chr13:36237441
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-6149A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237441 | ||||||
| chr13:36237511
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(36): Show | 52 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.546-6219T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237511 | ||||||
| chr13:36237589
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-6297C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237589 | ||||||
| chr13:36237627
|
A | G | 1 | a0002c0002t0002g0247 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.546-6335T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237627 | ||||||
| chr13:36237757
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.546-6465G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237757 | ||||||
| chr13:36237967
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-6675C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237967 | ||||||
| chr13:36237968
|
C | T | 8 | a0001c0005t0001g0058a0001c0005t0001g0059a0001c0005t0001g0060others(5): Show | 8 | HG01106.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-6676G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36237968 | ||||||
| chr13:36238089
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-6797T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238089 | ||||||
| chr13:36238169
|
T | C | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.546-6877A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238169 | ||||||
| chr13:36238196
|
T | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG02630.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.546-6904A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238196 | ||||||
| chr13:36238256
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.546-6964G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238256 | ||||||
| chr13:36238342
|
C | T | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.546-7050G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238342 | ||||||
| chr13:36238343
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-7051C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238343 | ||||||
| chr13:36238380
|
C | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-7088G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238380 | ||||||
| chr13:36238467
|
T | A | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.546-7175A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238467 | ||||||
| chr13:36238581
|
C | A | 8 | a0001c0005t0001g0058a0001c0005t0001g0059a0001c0005t0001g0060others(5): Show | 8 | HG01106.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-7289G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238581 | ||||||
| chr13:36238725
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-7433C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238725 | ||||||
| chr13:36238816
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.546-7524C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238816 | ||||||
| chr13:36238929
|
A | T | 100 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(97): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.546-7637T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36238929 | ||||||
| chr13:36239004
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.546-7712C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239004 | ||||||
| chr13:36239067
|
T | A | 1 | a0003c0006t0002g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.546-7775A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239067 | ||||||
| chr13:36239090
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-7798C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239090 | ||||||
| chr13:36239113
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.546-7821G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239113 | ||||||
| chr13:36239135
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.546-7843C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239135 | ||||||
| chr13:36239164
|
G | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 112 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.546-7872C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239164 | ||||||
| chr13:36239248
|
GA | G | 32 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(29): Show | 39 | HG00597.hp2 HG00738.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.546-7957delT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239248 | ||||||
| chr13:36239248
|
GAAA | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(232): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.546-7959_546-7957d others(5): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239248 | ||||||
| chr13:36239260
|
AAC | A | 18 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0056others(15): Show | 20 | HG00140.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.546-7970_546-7969d others(4): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239260 | ||||||
| chr13:36239385
|
C | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.546-8093G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239385 | ||||||
| chr13:36239486
|
C | G | 2 | a0002c0003t0002g0044a0002c0003t0002g0045 | 2 | HG00738.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.546-8194G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239486 | ||||||
| chr13:36239487
|
T | C | 1 | a0002c0003t0002g0038 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.546-8195A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239487 | ||||||
| chr13:36239598
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-8306C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239598 | ||||||
| chr13:36239604
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-8312C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239604 | ||||||
| chr13:36239622
|
A | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-8330T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239622 | ||||||
| chr13:36239832
|
C | CCA | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.546-8542_546-8541d others(4): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36239832 | ||||||
| chr13:36240287
|
A | T | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.545+8319T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240287 | ||||||
| chr13:36240291
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.545+8315A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240291 | ||||||
| chr13:36240294
|
A | C | 1 | a0001c0001t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.545+8312T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240294 | ||||||
| chr13:36240344
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+8262A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240344 | ||||||
| chr13:36240391
|
C | T | 8 | a0001c0005t0001g0058a0001c0005t0001g0059a0001c0005t0001g0060others(5): Show | 8 | HG01106.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+8215G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240391 | ||||||
| chr13:36240471
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.545+8135G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240471 | ||||||
| chr13:36240545
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+8061T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240545 | ||||||
| chr13:36240784
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.545+7822A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240784 | ||||||
| chr13:36240925
|
T | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0156a0001c0001t0001g0166 | 3 | NA18954.hp2 NA19066.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.545+7681A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240925 | ||||||
| chr13:36240952
|
C | T | 2 | a0002c0003t0003g0010a0004c0008t0003g0288 | 4 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+7654G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240952 | ||||||
| chr13:36240967
|
G | A | 39 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(36): Show | 48 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.545+7639C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240967 | ||||||
| chr13:36240988
|
G | A | 2 | a0002c0003t0003g0010a0004c0008t0003g0288 | 4 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+7618C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36240988 | ||||||
| chr13:36241087
|
T | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+7519A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36241087 | ||||||
| chr13:36241160
|
T | C | 2 | a0001c0001t0001g0074a0001c0004t0001g0274 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.545+7446A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36241160 | ||||||
| chr13:36241331
|
A | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+7275T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36241331 | ||||||
| chr13:36241382
|
G | GTCGC | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+7223_545+7224i others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36241382 | ||||||
| chr13:36241552
|
AT | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(38): Show | 59 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.545+7053delA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36241552 | ||||||
| chr13:36241587
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+7019A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36241587 | ||||||
| chr13:36241690
|
C | A | 1 | a0001c0005t0001g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.545+6916G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36241690 | ||||||
| chr13:36241738
|
TG | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+6867delC | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36241738 | ||||||
| chr13:36241778
|
A | G | 1 | a0002c0002t0002g0292 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.545+6828T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36241778 | ||||||
| chr13:36241808
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+6798A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36241808 | ||||||
| chr13:36242020
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+6586T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36242020 | ||||||
| chr13:36242193
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+6413T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36242193 | ||||||
| chr13:36242254
|
A | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+6352T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36242254 | ||||||
| chr13:36242280
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(84): Show | 121 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.545+6326T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36242280 | ||||||
| chr13:36242770
|
G | T | 23 | a0002c0003t0002g0016a0002c0003t0002g0017a0002c0003t0002g0018others(20): Show | 26 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.545+5836C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36242770 | ||||||
| chr13:36242985
|
G | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(70): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.545+5621C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36242985 | ||||||
| chr13:36242996
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.545+5610T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36242996 | ||||||
| chr13:36243094
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.545+5512A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243094 | ||||||
| chr13:36243122
|
G | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0103a0001c0001t0001g0135others(2): Show | 6 | HG01884.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.545+5484C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243122 | ||||||
| chr13:36243199
|
T | G | 1 | a0002c0003t0002g0190 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.545+5407A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243199 | ||||||
| chr13:36243270
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.545+5336G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243270 | ||||||
| chr13:36243297
|
C | T | 2 | a0002c0003t0003g0010a0004c0008t0003g0288 | 4 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+5309G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243297 | ||||||
| chr13:36243370
|
C | G | 100 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(97): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.545+5236G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243370 | ||||||
| chr13:36243400
|
TGAGGCAG others(19): Show |
T | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG01884.hp2 HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.545+5180_545+5205d others(28): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243400 | ||||||
| chr13:36243436
|
T | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+5170A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243436 | ||||||
| chr13:36243447
|
CAG | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+5157_545+5158d others(4): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243447 | ||||||
| chr13:36243510
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.545+5096A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243510 | ||||||
| chr13:36243533
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+5073T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243533 | ||||||
| chr13:36243567
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+5039T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243567 | ||||||
| chr13:36243581
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.545+5025G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243581 | ||||||
| chr13:36243582
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+5024C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243582 | ||||||
| chr13:36243635
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+4971A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243635 | ||||||
| chr13:36243669
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+4937T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243669 | ||||||
| chr13:36243710
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+4896T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243710 | ||||||
| chr13:36243714
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.545+4892C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243714 | ||||||
| chr13:36243714
|
G | C | 8 | a0001c0005t0001g0058a0001c0005t0001g0059a0001c0005t0001g0060others(5): Show | 8 | HG01106.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+4892C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243714 | ||||||
| chr13:36243894
|
T | C | 1 | a0002c0003t0003g0010 | 3 | HG03130.hp1 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.545+4712A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243894 | ||||||
| chr13:36243900
|
A | G | 100 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(97): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.545+4706T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243900 | ||||||
| chr13:36243920
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 112 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.545+4686G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243920 | ||||||
| chr13:36243943
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+4663G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36243943 | ||||||
| chr13:36244173
|
C | T | 1 | a0002c0002t0002g0251 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.545+4433G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36244173 | ||||||
| chr13:36244475
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+4131C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36244475 | ||||||
| chr13:36244565
|
G | A | 1 | a0002c0003t0002g0041 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.545+4041C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36244565 | ||||||
| chr13:36244599
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+4007A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36244599 | ||||||
| chr13:36244644
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.545+3962T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36244644 | ||||||
| chr13:36244671
|
AGAAG | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0029others(137): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.545+3931_545+3934d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36244671 | ||||||
| chr13:36244720
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+3886T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36244720 | ||||||
| chr13:36244777
|
CAGTGGTC others(54): Show |
C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(133): Show | 178 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.545+3768_545+3828d others(63): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36244777 | ||||||
| chr13:36244941
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+3665C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36244941 | ||||||
| chr13:36245181
|
A | G | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.545+3425T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36245181 | ||||||
| chr13:36245433
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.545+3173C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36245433 | ||||||
| chr13:36245488
|
C | CAG | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+3116_545+3117d others(4): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36245488 | ||||||
| chr13:36245678
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+2928C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36245678 | ||||||
| chr13:36245821
|
C | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+2785G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36245821 | ||||||
| chr13:36245940
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+2666C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36245940 | ||||||
| chr13:36246174
|
A | C | 1 | a0002c0002t0002g0267 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.545+2432T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246174 | ||||||
| chr13:36246223
|
C | G | 1 | a0002c0002t0002g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.545+2383G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246223 | ||||||
| chr13:36246301
|
A | G | 102 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(99): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.545+2305T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246301 | ||||||
| chr13:36246347
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.545+2259A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246347 | ||||||
| chr13:36246521
|
C | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+2085G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246521 | ||||||
| chr13:36246614
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.545+1992A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246614 | ||||||
| chr13:36246673
|
A | G | 1 | a0002c0003t0002g0175 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.545+1933T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246673 | ||||||
| chr13:36246711
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+1895G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246711 | ||||||
| chr13:36246721
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+1885A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246721 | ||||||
| chr13:36246961
|
C | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+1645G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246961 | ||||||
| chr13:36246989
|
C | T | 1 | a0001c0001t0001g0027 | 2 | HG00733.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.545+1617G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36246989 | ||||||
| chr13:36247010
|
G | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+1596C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247010 | ||||||
| chr13:36247137
|
A | G | 3 | a0001c0001t0001g0089a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG02630.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.545+1469T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247137 | ||||||
| chr13:36247261
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.545+1345A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247261 | ||||||
| chr13:36247416
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+1190A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247416 | ||||||
| chr13:36247491
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.545+1115A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247491 | ||||||
| chr13:36247516
|
GT | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(41): Show | 53 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.545+1089delA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247516 | ||||||
| chr13:36247539
|
C | A | 1 | a0001c0001t0001g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.545+1067G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247539 | ||||||
| chr13:36247739
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+867G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247739 | ||||||
| chr13:36247908
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0214 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.545+698T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247908 | ||||||
| chr13:36247930
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.545+676C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247930 | ||||||
| chr13:36247955
|
T | G | 5 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+651A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36247955 | ||||||
| chr13:36248028
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+578A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36248028 | ||||||
| chr13:36248238
|
C | G | 8 | a0001c0005t0001g0058a0001c0005t0001g0059a0001c0005t0001g0060others(5): Show | 8 | HG01106.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+368G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36248238 | ||||||
| chr13:36248238
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+368G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36248238 | ||||||
| chr13:36248261
|
G | A | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.545+345C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36248261 | ||||||
| chr13:36248388
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.545+218C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36248388 | ||||||
| chr13:36248476
|
A | G | 1 | a0002c0002t0002g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.545+130T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36248476 | ||||||
| chr13:36248574
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.545+32C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 7/7 | chr13 | 36248574 | ||||||
| chr13:36248704
|
G | T | 1 | a0001c0001t0001g0147 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.469-22C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36248704 | ||||||
| chr13:36248712
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-30G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36248712 | ||||||
| chr13:36248732
|
C | G | 1 | a0001c0001t0001g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.469-50G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36248732 | ||||||
| chr13:36248747
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-65G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36248747 | ||||||
| chr13:36248771
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-89G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36248771 | ||||||
| chr13:36248902
|
T | TA | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.469-221dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36248902 | ||||||
| chr13:36248999
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-317C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36248999 | ||||||
| chr13:36249004
|
C | G | 17 | a0002c0003t0002g0016a0002c0003t0002g0017a0002c0003t0002g0018others(14): Show | 20 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.469-322G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249004 | ||||||
| chr13:36249436
|
G | A | 103 | a0001c0001t0001g0097a0002c0002t0002g0003a0002c0002t0002g0006others(100): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.469-754C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249436 | ||||||
| chr13:36249462
|
T | C | 21 | a0002c0002t0002g0003a0002c0002t0002g0031a0002c0002t0002g0033others(18): Show | 28 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.469-780A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249462 | ||||||
| chr13:36249480
|
A | G | 1 | a0002c0002t0002g0269 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.469-798T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249480 | ||||||
| chr13:36249500
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-818C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249500 | ||||||
| chr13:36249502
|
G | A | 50 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(47): Show | 59 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.469-820C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249502 | ||||||
| chr13:36249594
|
A | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(47): Show | 59 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.469-912T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249594 | ||||||
| chr13:36249628
|
C | T | 74 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(71): Show | 89 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.469-946G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249628 | ||||||
| chr13:36249662
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.469-980A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249662 | ||||||
| chr13:36249730
|
G | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(39): Show | 51 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.469-1048C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249730 | ||||||
| chr13:36249740
|
T | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-1058A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249740 | ||||||
| chr13:36249742
|
TTAAG | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-1064_469-1061d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249742 | ||||||
| chr13:36249751
|
T | A | 5 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-1069A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249751 | ||||||
| chr13:36249951
|
A | AATTC | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-1273_469-1270d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249951 | ||||||
| chr13:36249970
|
C | A | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.469-1288G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249970 | ||||||
| chr13:36250050
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-1368C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250050 | ||||||
| chr13:36250129
|
G | A | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.469-1447C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250129 | ||||||
| chr13:36250150
|
A | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-1468T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250150 | ||||||
| chr13:36250155
|
G | A | 1 | a0001c0001t0001g0005 | 5 | HG00738.hp2 HG01192.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-1473C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250155 | ||||||
| chr13:36250197
|
A | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(288): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.469-1515T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250197 | ||||||
| chr13:36250251
|
T | C | 1 | a0002c0002t0002g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.469-1569A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250251 | ||||||
| chr13:36250315
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-1633T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250315 | ||||||
| chr13:36250433
|
C | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-1751G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250433 | ||||||
| chr13:36250593
|
A | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-1911T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250593 | ||||||
| chr13:36250703
|
C | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-2021G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250703 | ||||||
| chr13:36250844
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.469-2162A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250844 | ||||||
| chr13:36250911
|
T | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0066others(6): Show | 14 | HG00558.hp2 HG00609.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.469-2229A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250911 | ||||||
| chr13:36250970
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-2288A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250970 | ||||||
| chr13:36250977
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-2295T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36250977 | ||||||
| chr13:36251015
|
A | C | 1 | a0002c0003t0002g0018 | 2 | HG00099.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.469-2333T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251015 | ||||||
| chr13:36251071
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.469-2389C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251071 | ||||||
| chr13:36251088
|
G | A | 1 | a0002c0002t0003g0289 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.469-2406C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251088 | ||||||
| chr13:36251175
|
A | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(133): Show | 178 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.469-2493T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251175 | ||||||
| chr13:36251377
|
T | TTTA | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+2423_468+2425d others(5): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251377 | ||||||
| chr13:36251400
|
T | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+2403A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251400 | ||||||
| chr13:36251508
|
T | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+2295A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251508 | ||||||
| chr13:36251554
|
TA | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+2248delT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251554 | ||||||
| chr13:36251660
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.468+2143A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251660 | ||||||
| chr13:36251854
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+1949T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251854 | ||||||
| chr13:36251933
|
C | T | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.468+1870G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36251933 | ||||||
| chr13:36252097
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.468+1706A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36252097 | ||||||
| chr13:36252193
|
A | C | 2 | a0001c0005t0001g0062a0001c0005t0001g0064 | 2 | HG01106.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.468+1610T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36252193 | ||||||
| chr13:36252229
|
C | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(153): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.468+1574G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36252229 | ||||||
| chr13:36252234
|
G | A | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.468+1569C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36252234 | ||||||
| chr13:36252525
|
A | G | 1 | a0002c0002t0002g0246 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.468+1278T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36252525 | ||||||
| chr13:36252643
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+1160G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36252643 | ||||||
| chr13:36252688
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(36): Show | 52 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.468+1115T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36252688 | ||||||
| chr13:36252851
|
T | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+952A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36252851 | ||||||
| chr13:36253008
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+795T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253008 | ||||||
| chr13:36253028
|
CA | C | 71 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(68): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.468+774delT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253028 | ||||||
| chr13:36253038
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+765C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253038 | ||||||
| chr13:36253045
|
T | C | 1 | a0002c0002t0002g0290 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.468+758A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253045 | ||||||
| chr13:36253086
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.468+717C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253086 | ||||||
| chr13:36253149
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+654A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253149 | ||||||
| chr13:36253261
|
T | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+542A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253261 | ||||||
| chr13:36253300
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+503T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253300 | ||||||
| chr13:36253329
|
T | C | 51 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(48): Show | 60 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.468+474A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253329 | ||||||
| chr13:36253340
|
CT | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(187): Show | 243 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.468+462delA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253340 | ||||||
| chr13:36253360
|
ATGGAGTC others(18): Show |
A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(185): Show | 239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.468+418_468+442del others(25): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253360 | ||||||
| chr13:36253420
|
C | CCT | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+381_468+382dup others(2): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253420 | ||||||
| chr13:36253560
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+243A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253560 | ||||||
| chr13:36253635
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+168G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253635 | ||||||
| chr13:36253651
|
C | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+152G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253651 | ||||||
| chr13:36253654
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+149C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253654 | ||||||
| chr13:36253696
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+107G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253696 | ||||||
| chr13:36253759
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.468+44G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253759 | ||||||
| chr13:36253793
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.468+10T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253793 | ||||||
| chr13:36253892
|
T | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0154a0001c0001t0001g0157others(3): Show | 8 | HG00597.hp2 HG02074.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-36A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 5/7 | chr13 | 36253892 | ||||||
| chr13:36253955
|
G | GTTTTGTA others(4): Show |
104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.414+89_414+90insTG others(9): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 5/7 | chr13 | 36253955 | ||||||
| chr13:36254230
|
C | T | 3 | a0002c0002t0002g0223a0002c0002t0002g0224a0002c0003t0002g0075 | 3 | HG02735.hp2 HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.316-87G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254230 | ||||||
| chr13:36254270
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-127T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254270 | ||||||
| chr13:36254274
|
A | AATT | 25 | a0002c0002t0002g0219a0002c0003t0002g0016a0002c0003t0002g0017others(22): Show | 30 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.316-132_316-131ins others(3): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254274 | ||||||
| chr13:36254274
|
A | AATTT | 66 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(63): Show | 81 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.316-132_316-131ins others(4): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254274 | ||||||
| chr13:36254274
|
A | AATTTT | 11 | a0002c0002t0002g0218a0002c0002t0002g0233a0002c0002t0002g0246others(8): Show | 11 | HG00597.hp1 HG00673.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.316-132_316-131ins others(5): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254274 | ||||||
| chr13:36254275
|
C | CT | 13 | a0001c0001t0001g0070a0001c0001t0001g0087a0001c0001t0001g0100others(10): Show | 13 | HG01106.hp2 HG02135.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.316-133dupA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254275 | ||||||
| chr13:36254275
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-132G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254275 | ||||||
| chr13:36254275
|
CT | C | 6 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0143others(3): Show | 6 | HG01255.hp1 HG01516.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-133delA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254275 | ||||||
| chr13:36254405
|
A | C | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG01884.hp2 HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.316-262T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254405 | ||||||
| chr13:36254476
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.316-333A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254476 | ||||||
| chr13:36254572
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(133): Show | 178 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.316-429C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254572 | ||||||
| chr13:36254638
|
A | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(32): Show | 47 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.316-495T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254638 | ||||||
| chr13:36254645
|
G | A | 1 | a0002c0002t0002g0234 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.316-502C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254645 | ||||||
| chr13:36254671
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(133): Show | 178 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.316-528T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254671 | ||||||
| chr13:36254701
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-558G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254701 | ||||||
| chr13:36254711
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-568A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254711 | ||||||
| chr13:36254721
|
T | A | 100 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(97): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.316-578A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254721 | ||||||
| chr13:36254751
|
T | G | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.316-608A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254751 | ||||||
| chr13:36254766
|
T | C | 41 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(38): Show | 59 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.316-623A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254766 | ||||||
| chr13:36254872
|
A | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-729T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254872 | ||||||
| chr13:36254948
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-805T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36254948 | ||||||
| chr13:36255011
|
T | C | 2 | a0002c0003t0003g0010a0004c0008t0003g0288 | 4 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-868A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255011 | ||||||
| chr13:36255072
|
C | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-929G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255072 | ||||||
| chr13:36255121
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-978C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255121 | ||||||
| chr13:36255147
|
A | G | 1 | a0002c0002t0002g0241 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.316-1004T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255147 | ||||||
| chr13:36255164
|
A | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-1021T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255164 | ||||||
| chr13:36255237
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | NA19009.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.316-1094G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255237 | ||||||
| chr13:36255389
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-1246A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255389 | ||||||
| chr13:36255424
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.316-1281C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255424 | ||||||
| chr13:36255433
|
G | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0066a0001c0001t0001g0069others(5): Show | 9 | HG00558.hp2 NA18747.hp2 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.316-1290C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255433 | ||||||
| chr13:36255453
|
A | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.316-1310T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255453 | ||||||
| chr13:36255557
|
C | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-1414G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255557 | ||||||
| chr13:36255659
|
T | TA | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(72): Show | 93 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.316-1517dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255659 | ||||||
| chr13:36255659
|
T | TAAAA | 28 | a0002c0002t0002g0219a0002c0002t0002g0229a0002c0002t0002g0255others(25): Show | 31 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.316-1520_316-1517d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255659 | ||||||
| chr13:36255659
|
T | TAAAAA | 60 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(57): Show | 74 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.316-1521_316-1517d others(7): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255659 | ||||||
| chr13:36255659
|
T | TAAAAAA | 14 | a0002c0002t0002g0032a0002c0002t0002g0223a0002c0002t0002g0224others(11): Show | 15 | HG00423.hp2 HG01175.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.316-1522_316-1517d others(8): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255659 | ||||||
| chr13:36255692
|
G | A | 1 | a0002c0003t0002g0190 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.316-1549C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255692 | ||||||
| chr13:36255692
|
G | C | 1 | a0002c0002t0002g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.316-1549C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255692 | ||||||
| chr13:36255769
|
A | T | 103 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(100): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.316-1626T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255769 | ||||||
| chr13:36255771
|
C | T | 1 | a0002c0002t0002g0278 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.316-1628G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255771 | ||||||
| chr13:36255825
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-1682G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255825 | ||||||
| chr13:36255884
|
C | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-1741G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255884 | ||||||
| chr13:36255912
|
C | T | 3 | a0002c0002t0002g0262a0002c0002t0002g0267a0002c0002t0002g0290 | 3 | HG00408.hp1 HG03942.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.316-1769G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255912 | ||||||
| chr13:36255927
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.316-1784G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255927 | ||||||
| chr13:36255933
|
A | G | 2 | a0001c0004t0001g0009a0001c0004t0001g0276 | 5 | NA18954.hp1 NA18971.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-1790T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255933 | ||||||
| chr13:36255934
|
C | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-1791G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255934 | ||||||
| chr13:36256022
|
GC | G | 71 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(68): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.316-1880delG | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256022 | ||||||
| chr13:36256062
|
G | A | 1 | a0002c0002t0002g0267 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.316-1919C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256062 | ||||||
| chr13:36256107
|
G | A | 1 | a0002c0002t0002g0254 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.316-1964C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256107 | ||||||
| chr13:36256161
|
C | T | 24 | a0002c0003t0002g0016a0002c0003t0002g0017a0002c0003t0002g0018others(21): Show | 27 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.316-2018G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256161 | ||||||
| chr13:36256174
|
AGTGT | A | 8 | a0002c0002t0002g0033a0002c0002t0002g0228a0002c0002t0002g0229others(5): Show | 9 | HG02027.hp1 NA18940.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.316-2035_316-2032d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256174 | ||||||
| chr13:36256234
|
C | T | 51 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(48): Show | 60 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.316-2091G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256234 | ||||||
| chr13:36256262
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.316-2119C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256262 | ||||||
| chr13:36256290
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0177 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.316-2147C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256290 | ||||||
| chr13:36256292
|
C | A | 1 | a0001c0001t0001g0165 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.316-2149G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256292 | ||||||
| chr13:36256374
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316-2231A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256374 | ||||||
| chr13:36256455
|
C | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG02615.hp1 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.316-2312G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256455 | ||||||
| chr13:36256467
|
G | C | 1 | a0003c0006t0002g0050 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.316-2324C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256467 | ||||||
| chr13:36256525
|
T | C | 101 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(98): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.316-2382A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256525 | ||||||
| chr13:36256551
|
A | AT | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-2409dupA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256551 | ||||||
| chr13:36256748
|
C | T | 100 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(97): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.316-2605G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256748 | ||||||
| chr13:36256757
|
G | A | 1 | a0002c0002t0002g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.316-2614C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256757 | ||||||
| chr13:36256760
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.316-2617G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256760 | ||||||
| chr13:36256812
|
T | C | 1 | a0002c0003t0002g0187 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.316-2669A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36256812 | ||||||
| chr13:36257019
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-2876A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257019 | ||||||
| chr13:36257028
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.316-2885C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257028 | ||||||
| chr13:36257098
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-2955A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257098 | ||||||
| chr13:36257122
|
AC | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-2980delG | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257122 | ||||||
| chr13:36257145
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.316-3002A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257145 | ||||||
| chr13:36257160
|
T | G | 2 | a0002c0003t0003g0010a0004c0008t0003g0288 | 4 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-3017A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257160 | ||||||
| chr13:36257239
|
T | C | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.316-3096A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257239 | ||||||
| chr13:36257299
|
C | G | 1 | a0002c0003t0002g0075 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.316-3156G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257299 | ||||||
| chr13:36257387
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-3244C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257387 | ||||||
| chr13:36257505
|
A | AC | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.316-3363dupG | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257505 | ||||||
| chr13:36257516
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.316-3373T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257516 | ||||||
| chr13:36257626
|
G | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-3483C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257626 | ||||||
| chr13:36257628
|
G | A | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316-3485C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257628 | ||||||
| chr13:36257709
|
AG | A | 4 | a0002c0002t0002g0229a0002c0003t0002g0176a0002c0003t0003g0010others(1): Show | 6 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-3567delC | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257709 | ||||||
| chr13:36257710
|
G | A | 100 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(97): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.316-3567C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257710 | ||||||
| chr13:36257994
|
G | A | 2 | a0001c0001t0001g0161a0002c0002t0002g0034 | 3 | HG03490.hp2 HG03492.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.316-3851C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36257994 | ||||||
| chr13:36258086
|
A | AC | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-3944dupG | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258086 | ||||||
| chr13:36258239
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0110a0001c0001t0001g0195others(1): Show | 6 | HG02965.hp1 HG03209.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.316-4096G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258239 | ||||||
| chr13:36258345
|
A | G | 75 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(72): Show | 90 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.316-4202T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258345 | ||||||
| chr13:36258468
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.316-4325C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258468 | ||||||
| chr13:36258749
|
C | CT | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-4607_316-4606i others(3): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258749 | ||||||
| chr13:36258838
|
C | A | 1 | a0001c0001t0001g0097 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.316-4695G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258838 | ||||||
| chr13:36258844
|
C | A | 1 | a0002c0003t0002g0043 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.316-4701G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258844 | ||||||
| chr13:36258942
|
C | A | 1 | a0001c0001t0001g0106 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.316-4799G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258942 | ||||||
| chr13:36258943
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.316-4800T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258943 | ||||||
| chr13:36258944
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.316-4801A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258944 | ||||||
| chr13:36258946
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.316-4803A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36258946 | ||||||
| chr13:36259037
|
G | A | 103 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(100): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.316-4894C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259037 | ||||||
| chr13:36259054
|
G | A | 8 | a0001c0005t0001g0058a0001c0005t0001g0059a0001c0005t0001g0060others(5): Show | 8 | HG01106.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-4911C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259054 | ||||||
| chr13:36259175
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-5032G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259175 | ||||||
| chr13:36259205
|
C | A | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.316-5062G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259205 | ||||||
| chr13:36259214
|
C | G | 1 | a0002c0002t0002g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.316-5071G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259214 | ||||||
| chr13:36259235
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-5092T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259235 | ||||||
| chr13:36259533
|
G | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-5390C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259533 | ||||||
| chr13:36259584
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.316-5441A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259584 | ||||||
| chr13:36259629
|
A | C | 3 | a0002c0003t0002g0016a0002c0003t0002g0039a0002c0003t0002g0185 | 4 | HG02683.hp1 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-5486T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259629 | ||||||
| chr13:36259629
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(36): Show | 52 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.316-5486T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259629 | ||||||
| chr13:36259680
|
TCACGACC others(28): Show |
T | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0098 | 3 | NA18948.hp2 NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.316-5572_316-5538d others(37): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259680 | ||||||
| chr13:36259683
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.316-5540G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259683 | ||||||
| chr13:36259748
|
G | C | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.316-5605C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259748 | ||||||
| chr13:36259859
|
A | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-5716T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259859 | ||||||
| chr13:36259955
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-5812A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36259955 | ||||||
| chr13:36260185
|
G | C | 1 | a0001c0001t0001g0202 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.316-6042C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36260185 | ||||||
| chr13:36260456
|
T | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-6313A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36260456 | ||||||
| chr13:36260478
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-6335C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36260478 | ||||||
| chr13:36260709
|
A | G | 19 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0046others(16): Show | 22 | HG00597.hp2 HG01192.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.316-6566T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36260709 | ||||||
| chr13:36260776
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-6633T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36260776 | ||||||
| chr13:36260787
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-6644A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36260787 | ||||||
| chr13:36260832
|
C | T | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.316-6689G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36260832 | ||||||
| chr13:36260890
|
T | C | 2 | a0002c0002t0002g0260a0002c0002t0002g0268 | 2 | NA18970.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.316-6747A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36260890 | ||||||
| chr13:36260961
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.316-6818C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36260961 | ||||||
| chr13:36261001
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-6858T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261001 | ||||||
| chr13:36261082
|
C | T | 2 | a0002c0003t0003g0010a0004c0008t0003g0288 | 4 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-6939G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261082 | ||||||
| chr13:36261111
|
TGTGTAAG others(14): Show |
T | 1 | a0002c0002t0002g0284 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.316-6989_316-6969d others(23): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261111 | ||||||
| chr13:36261237
|
C | A | 1 | a0002c0002t0003g0289 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.316-7094G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261237 | ||||||
| chr13:36261237
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.316-7094G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261237 | ||||||
| chr13:36261246
|
A | G | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-7103T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261246 | ||||||
| chr13:36261348
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.316-7205T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261348 | ||||||
| chr13:36261543
|
C | T | 1 | a0001c0004t0001g0265 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.316-7400G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261543 | ||||||
| chr13:36261581
|
T | C | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-7438A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261581 | ||||||
| chr13:36261596
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.316-7453C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261596 | ||||||
| chr13:36261619
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.316-7476A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261619 | ||||||
| chr13:36261753
|
C | T | 1 | a0002c0002t0002g0253 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.316-7610G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261753 | ||||||
| chr13:36261786
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.316-7643C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261786 | ||||||
| chr13:36261801
|
C | CACTGGGC others(4): Show |
3 | a0001c0001t0001g0147a0001c0001t0001g0156a0001c0001t0001g0166 | 3 | NA18954.hp2 NA19066.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.316-7659_316-7658i others(13): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261801 | ||||||
| chr13:36261839
|
G | T | 1 | a0001c0001t0001g0202 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.316-7696C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36261839 | ||||||
| chr13:36262008
|
T | A | 100 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(97): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.316-7865A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262008 | ||||||
| chr13:36262062
|
T | A | 100 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(97): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.316-7919A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262062 | ||||||
| chr13:36262128
|
G | C | 5 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-7985C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262128 | ||||||
| chr13:36262250
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.316-8107G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262250 | ||||||
| chr13:36262263
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-8120C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262263 | ||||||
| chr13:36262296
|
A | AC | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-8154_316-8153i others(3): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262296 | ||||||
| chr13:36262437
|
C | T | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-8294G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262437 | ||||||
| chr13:36262524
|
C | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 52 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.316-8381G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262524 | ||||||
| chr13:36262665
|
G | A | 104 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(101): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-8522C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262665 | ||||||
| chr13:36262738
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.316-8595A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262738 | ||||||
| chr13:36262779
|
C | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | NA18982.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.316-8636G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262779 | ||||||
| chr13:36262911
|
C | G | 1 | a0001c0004t0001g0276 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.316-8768G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262911 | ||||||
| chr13:36262932
|
G | T | 37 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0025others(34): Show | 42 | HG00140.hp2 HG00597.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.316-8789C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36262932 | ||||||
| chr13:36263032
|
C | A | 2 | a0002c0003t0003g0010a0004c0008t0003g0288 | 4 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-8889G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36263032 | ||||||
| chr13:36263207
|
T | TTAGA | 102 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0030others(99): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.316-9068_316-9065d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36263207 | ||||||
| chr13:36263850
|
C | A | 35 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0025others(32): Show | 40 | HG00140.hp2 HG01106.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.316-9707G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36263850 | ||||||
| chr13:36263862
|
C | T | 96 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0001g0078others(93): Show | 119 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.316-9719G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36263862 | ||||||
| chr13:36263922
|
T | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0070others(14): Show | 22 | HG00609.hp2 HG02071.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.316-9779A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36263922 | ||||||
| chr13:36263935
|
C | T | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.316-9792G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36263935 | ||||||
| chr13:36263937
|
C | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0026others(40): Show | 54 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.316-9794G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36263937 | ||||||
| chr13:36264010
|
T | C | 1 | a0002c0002t0002g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.316-9867A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36264010 | ||||||
| chr13:36264133
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.316-9990G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36264133 | ||||||
| chr13:36264223
|
T | C | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.316-10080A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36264223 | ||||||
| chr13:36264325
|
T | C | 1 | a0001c0001t0001g0007 | 4 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-10182A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36264325 | ||||||
| chr13:36264460
|
C | T | 90 | a0001c0001t0001g0108a0001c0004t0001g0009a0001c0004t0001g0015others(87): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.316-10317G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36264460 | ||||||
| chr13:36264537
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-10394A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36264537 | ||||||
| chr13:36264770
|
G | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-10627C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36264770 | ||||||
| chr13:36264784
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-10641G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36264784 | ||||||
| chr13:36264826
|
T | C | 1 | a0002c0002t0002g0272 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.316-10683A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36264826 | ||||||
| chr13:36264888
|
G | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-10745C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36264888 | ||||||
| chr13:36265064
|
G | A | 1 | a0001c0001t0001g0057 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.316-10921C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265064 | ||||||
| chr13:36265143
|
C | A | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.316-11000G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265143 | ||||||
| chr13:36265165
|
G | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-11022C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265165 | ||||||
| chr13:36265174
|
G | A | 1 | a0002c0002t0002g0254 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.316-11031C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265174 | ||||||
| chr13:36265282
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.316-11139A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265282 | ||||||
| chr13:36265325
|
C | T | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.316-11182G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265325 | ||||||
| chr13:36265401
|
A | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(77): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.316-11258T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265401 | ||||||
| chr13:36265438
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0101 | 2 | NA18962.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.316-11295T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265438 | ||||||
| chr13:36265467
|
G | A | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316-11324C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265467 | ||||||
| chr13:36265477
|
A | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-11334T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265477 | ||||||
| chr13:36265533
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-11390G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265533 | ||||||
| chr13:36265579
|
T | C | 90 | a0001c0001t0001g0215a0001c0004t0001g0009a0001c0004t0001g0015others(87): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.316-11436A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265579 | ||||||
| chr13:36265596
|
G | C | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316-11453C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265596 | ||||||
| chr13:36265753
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-11610T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265753 | ||||||
| chr13:36265779
|
T | C | 2 | a0001c0004t0001g0293a0004c0008t0003g0288 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.316-11636A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265779 | ||||||
| chr13:36265857
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-11714G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265857 | ||||||
| chr13:36265945
|
A | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-11802T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36265945 | ||||||
| chr13:36266173
|
C | T | 1 | a0002c0003t0002g0190 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.316-12030G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36266173 | ||||||
| chr13:36266253
|
G | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-12110C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36266253 | ||||||
| chr13:36266488
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.316-12345G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36266488 | ||||||
| chr13:36266599
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.316-12456G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36266599 | ||||||
| chr13:36266645
|
C | T | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.316-12502G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36266645 | ||||||
| chr13:36267027
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-12884T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267027 | ||||||
| chr13:36267075
|
C | G | 1 | a0001c0001t0001g0021 | 2 | HG02132.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.316-12932G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267075 | ||||||
| chr13:36267188
|
T | C | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.316-13045A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267188 | ||||||
| chr13:36267289
|
A | G | 2 | a0002c0002t0002g0245a0002c0002t0002g0272 | 2 | HG00099.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.316-13146T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267289 | ||||||
| chr13:36267322
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-13179T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267322 | ||||||
| chr13:36267332
|
G | C | 79 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0024others(76): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.316-13189C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267332 | ||||||
| chr13:36267333
|
C | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-13190G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267333 | ||||||
| chr13:36267352
|
C | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-13209G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267352 | ||||||
| chr13:36267474
|
A | G | 87 | a0001c0001t0001g0074a0001c0004t0001g0009a0001c0004t0001g0015others(84): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.316-13331T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267474 | ||||||
| chr13:36267534
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(32): Show | 51 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.316-13391A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267534 | ||||||
| chr13:36267561
|
T | C | 1 | a0002c0002t0002g0227 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.316-13418A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267561 | ||||||
| chr13:36267656
|
A | T | 1 | a0001c0001t0001g0105 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.316-13513T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267656 | ||||||
| chr13:36267963
|
A | T | 1 | a0001c0004t0001g0264 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.316-13820T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36267963 | ||||||
| chr13:36268069
|
C | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-13926G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268069 | ||||||
| chr13:36268086
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-13943T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268086 | ||||||
| chr13:36268166
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.316-14023T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268166 | ||||||
| chr13:36268249
|
A | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0107others(27): Show | 37 | HG00323.hp1 HG00621.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.316-14106T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268249 | ||||||
| chr13:36268301
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.316-14158T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268301 | ||||||
| chr13:36268547
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.316-14404G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268547 | ||||||
| chr13:36268616
|
C | G | 3 | a0002c0002t0002g0220a0002c0002t0002g0232a0002c0002t0002g0244 | 3 | HG02615.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.316-14473G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268616 | ||||||
| chr13:36268648
|
C | CA | 87 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(84): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.316-14506dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268648 | ||||||
| chr13:36268724
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0177 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.316-14581A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268724 | ||||||
| chr13:36268836
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.315+14633C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268836 | ||||||
| chr13:36268860
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.315+14609A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268860 | ||||||
| chr13:36268920
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+14549A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268920 | ||||||
| chr13:36268997
|
C | T | 1 | a0002c0002t0002g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.315+14472G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36268997 | ||||||
| chr13:36269107
|
T | TA | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+14361dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36269107 | ||||||
| chr13:36269121
|
T | A | 1 | a0001c0001t0001g0091 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.315+14348A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36269121 | ||||||
| chr13:36269187
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+14282A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36269187 | ||||||
| chr13:36269235
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.315+14234G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36269235 | ||||||
| chr13:36269260
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.315+14209A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36269260 | ||||||
| chr13:36269426
|
A | T | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.315+14043T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36269426 | ||||||
| chr13:36269940
|
G | GAA | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+13528_315+1352 others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36269940 | ||||||
| chr13:36269977
|
C | T | 2 | a0002c0003t0002g0044a0002c0003t0002g0045 | 2 | HG00738.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.315+13492G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36269977 | ||||||
| chr13:36270039
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.315+13430T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270039 | ||||||
| chr13:36270144
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+13325T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270144 | ||||||
| chr13:36270151
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.315+13318G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270151 | ||||||
| chr13:36270210
|
T | TAAC | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+13258_315+1325 others(7): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270210 | ||||||
| chr13:36270246
|
A | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+13223T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270246 | ||||||
| chr13:36270268
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+13201G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270268 | ||||||
| chr13:36270292
|
C | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+13177G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270292 | ||||||
| chr13:36270318
|
T | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+13151A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270318 | ||||||
| chr13:36270602
|
C | A | 1 | a0001c0001t0001g0069 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.315+12867G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270602 | ||||||
| chr13:36270790
|
T | TA | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+12678dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270790 | ||||||
| chr13:36270997
|
G | A | 5 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+12472C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36270997 | ||||||
| chr13:36271184
|
G | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+12285C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271184 | ||||||
| chr13:36271247
|
C | A | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.315+12222G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271247 | ||||||
| chr13:36271265
|
G | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+12204C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271265 | ||||||
| chr13:36271333
|
T | C | 1 | a0002c0002t0002g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.315+12136A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271333 | ||||||
| chr13:36271345
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+12124G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271345 | ||||||
| chr13:36271378
|
C | T | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315+12091G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271378 | ||||||
| chr13:36271381
|
T | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+12088A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271381 | ||||||
| chr13:36271442
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.315+12027T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271442 | ||||||
| chr13:36271477
|
T | C | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.315+11992A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271477 | ||||||
| chr13:36271581
|
A | C | 3 | a0002c0003t0002g0053a0002c0003t0002g0054a0002c0003t0002g0055 | 3 | HG02896.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.315+11888T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271581 | ||||||
| chr13:36271650
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.315+11819G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271650 | ||||||
| chr13:36271749
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+11720A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271749 | ||||||
| chr13:36271867
|
G | A | 1 | a0002c0002t0002g0222 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.315+11602C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271867 | ||||||
| chr13:36271951
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+11518T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271951 | ||||||
| chr13:36271952
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 5 | HG01106.hp1 HG01123.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+11517C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271952 | ||||||
| chr13:36271958
|
G | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+11511C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271958 | ||||||
| chr13:36271964
|
C | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+11505G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36271964 | ||||||
| chr13:36272002
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+11467A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272002 | ||||||
| chr13:36272053
|
C | T | 4 | a0002c0003t0002g0040a0002c0003t0002g0048a0002c0003t0002g0051others(1): Show | 4 | HG00733.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+11416G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272053 | ||||||
| chr13:36272054
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(30): Show | 45 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.315+11415C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272054 | ||||||
| chr13:36272084
|
C | CA | 89 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0004t0001g0009others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+11384dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272084 | ||||||
| chr13:36272103
|
A | AT | 88 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(85): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.315+11365_315+1136 others(5): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272103 | ||||||
| chr13:36272103
|
A | ATAAAATA others(4): Show |
1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+11365_315+1136 others(15): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272103 | ||||||
| chr13:36272110
|
AAT | A | 88 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(85): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.315+11357_315+1135 others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272110 | ||||||
| chr13:36272115
|
A | T | 88 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(85): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.315+11354T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272115 | ||||||
| chr13:36272116
|
T | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+11353A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272116 | ||||||
| chr13:36272152
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+11317A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272152 | ||||||
| chr13:36272220
|
CA | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(174): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.315+11248delT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272220 | ||||||
| chr13:36272233
|
C | A | 1 | a0002c0002t0002g0036 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.315+11236G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272233 | ||||||
| chr13:36272251
|
G | T | 1 | a0002c0003t0003g0010 | 3 | HG03130.hp1 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.315+11218C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272251 | ||||||
| chr13:36272267
|
T | A | 81 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.315+11202A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272267 | ||||||
| chr13:36272335
|
T | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+11134A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272335 | ||||||
| chr13:36272381
|
G | T | 1 | a0001c0001t0001g0163 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.315+11088C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272381 | ||||||
| chr13:36272426
|
A | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(24): Show | 39 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.315+11043T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272426 | ||||||
| chr13:36272511
|
A | G | 4 | a0002c0003t0002g0016a0002c0003t0002g0038a0002c0003t0002g0039others(1): Show | 5 | HG02602.hp2 HG02683.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+10958T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272511 | ||||||
| chr13:36272536
|
A | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+10933T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272536 | ||||||
| chr13:36272832
|
A | C | 1 | a0002c0002t0002g0222 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.315+10637T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272832 | ||||||
| chr13:36272864
|
T | C | 2 | a0002c0002t0002g0291a0002c0002t0002g0292 | 2 | NA18943.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.315+10605A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36272864 | ||||||
| chr13:36273193
|
T | C | 1 | a0002c0002t0002g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.315+10276A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36273193 | ||||||
| chr13:36273310
|
T | C | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315+10159A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36273310 | ||||||
| chr13:36273312
|
A | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+10157T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36273312 | ||||||
| chr13:36273558
|
C | T | 1 | a0001c0001t0001g0020 | 2 | NA19009.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.315+9911G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36273558 | ||||||
| chr13:36273627
|
A | G | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.315+9842T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36273627 | ||||||
| chr13:36273686
|
C | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+9783G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36273686 | ||||||
| chr13:36273746
|
G | A | 1 | a0002c0003t0002g0052 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.315+9723C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36273746 | ||||||
| chr13:36273749
|
C | G | 1 | a0002c0002t0002g0261 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.315+9720G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36273749 | ||||||
| chr13:36274050
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+9419A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274050 | ||||||
| chr13:36274116
|
A | G | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG01884.hp2 HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.315+9353T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274116 | ||||||
| chr13:36274311
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+9158A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274311 | ||||||
| chr13:36274380
|
T | C | 19 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(16): Show | 25 | HG00408.hp1 HG01981.hp1 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.315+9089A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274380 | ||||||
| chr13:36274427
|
C | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+9042G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274427 | ||||||
| chr13:36274596
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+8873A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274596 | ||||||
| chr13:36274668
|
A | G | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+8801T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274668 | ||||||
| chr13:36274727
|
T | C | 1 | a0002c0002t0002g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.315+8742A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274727 | ||||||
| chr13:36274868
|
A | AT | 108 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(105): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.315+8600dupA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274868 | ||||||
| chr13:36274868
|
A | ATT | 43 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(40): Show | 62 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.315+8599_315+8600d others(4): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274868 | ||||||
| chr13:36274868
|
A | ATTT | 21 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0110others(18): Show | 21 | HG00597.hp2 HG01109.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.315+8598_315+8600d others(5): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274868 | ||||||
| chr13:36274868
|
A | ATTTT | 64 | a0001c0001t0001g0029a0001c0001t0001g0111a0001c0004t0001g0009others(61): Show | 85 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.315+8597_315+8600d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274868 | ||||||
| chr13:36274868
|
A | ATTTTT | 21 | a0001c0004t0001g0240a0001c0004t0001g0258a0001c0004t0001g0259others(18): Show | 22 | HG00408.hp1 HG00642.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.315+8596_315+8600d others(7): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274868 | ||||||
| chr13:36274868
|
AT | A | 6 | a0001c0001t0001g0194a0001c0005t0001g0059a0001c0005t0001g0060others(3): Show | 6 | HG01106.hp2 HG01109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+8600delA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274868 | ||||||
| chr13:36274958
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.315+8511A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274958 | ||||||
| chr13:36274959
|
G | A | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315+8510C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274959 | ||||||
| chr13:36275058
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.315+8411G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36275058 | ||||||
| chr13:36275093
|
C | A | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+8376G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36275093 | ||||||
| chr13:36275147
|
G | A | 90 | a0001c0001t0001g0204a0001c0004t0001g0009a0001c0004t0001g0015others(87): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.315+8322C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36275147 | ||||||
| chr13:36275208
|
A | C | 4 | a0001c0004t0001g0293a0001c0005t0001g0060a0001c0005t0001g0065others(1): Show | 4 | HG02723.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+8261T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36275208 | ||||||
| chr13:36275353
|
T | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+8116A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36275353 | ||||||
| chr13:36275402
|
A | C | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+8067T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36275402 | ||||||
| chr13:36275843
|
A | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+7626T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36275843 | ||||||
| chr13:36275875
|
G | A | 87 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(84): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.315+7594C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36275875 | ||||||
| chr13:36275987
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.315+7482G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36275987 | ||||||
| chr13:36276088
|
C | A | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.315+7381G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276088 | ||||||
| chr13:36276309
|
G | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+7160C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276309 | ||||||
| chr13:36276328
|
C | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094 | 3 | NA18951.hp1 NA18955.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.315+7141G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276328 | ||||||
| chr13:36276337
|
A | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+7132T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276337 | ||||||
| chr13:36276352
|
A | T | 1 | a0002c0002t0002g0239 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.315+7117T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276352 | ||||||
| chr13:36276396
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.315+7073C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276396 | ||||||
| chr13:36276691
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.315+6778A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276691 | ||||||
| chr13:36276790
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.315+6679T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276790 | ||||||
| chr13:36276805
|
GC | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+6663delG | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276805 | ||||||
| chr13:36276832
|
G | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+6637C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276832 | ||||||
| chr13:36276896
|
G | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+6573C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276896 | ||||||
| chr13:36276942
|
C | T | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315+6527G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36276942 | ||||||
| chr13:36277262
|
T | C | 1 | a0002c0002t0003g0289 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.315+6207A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277262 | ||||||
| chr13:36277321
|
G | A | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.315+6148C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277321 | ||||||
| chr13:36277598
|
A | T | 3 | a0002c0003t0002g0016a0002c0003t0002g0039a0002c0003t0002g0185 | 4 | HG02683.hp1 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+5871T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277598 | ||||||
| chr13:36277737
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(24): Show | 39 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.315+5732C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277737 | ||||||
| chr13:36277746
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315+5723A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277746 | ||||||
| chr13:36277786
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+5683T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277786 | ||||||
| chr13:36277838
|
G | A | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315+5631C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277838 | ||||||
| chr13:36277896
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.315+5573C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277896 | ||||||
| chr13:36277918
|
C | A | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.315+5551G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277918 | ||||||
| chr13:36277931
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.315+5538G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277931 | ||||||
| chr13:36277944
|
C | CA | 6 | a0001c0001t0001g0127a0001c0001t0001g0212a0001c0001t0001g0213others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+5524dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277944 | ||||||
| chr13:36277944
|
CA | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0102others(3): Show | 6 | HG01168.hp1 HG01257.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+5524delT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277944 | ||||||
| chr13:36277944
|
CAA | C | 88 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(85): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.315+5523_315+5524d others(4): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277944 | ||||||
| chr13:36277962
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.315+5507C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36277962 | ||||||
| chr13:36278111
|
G | T | 1 | a0001c0001t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.315+5358C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36278111 | ||||||
| chr13:36278188
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315+5281C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36278188 | ||||||
| chr13:36278458
|
G | T | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+5011C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36278458 | ||||||
| chr13:36278779
|
G | T | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.315+4690C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36278779 | ||||||
| chr13:36278800
|
G | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | NA18945.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.315+4669C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36278800 | ||||||
| chr13:36278820
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+4649T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36278820 | ||||||
| chr13:36278913
|
T | C | 4 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG02055.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+4556A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36278913 | ||||||
| chr13:36278950
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.315+4519C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36278950 | ||||||
| chr13:36279102
|
T | TA | 87 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(84): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.315+4366dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36279102 | ||||||
| chr13:36279135
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.315+4334G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36279135 | ||||||
| chr13:36279228
|
C | A | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.315+4241G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36279228 | ||||||
| chr13:36279314
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.315+4155A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36279314 | ||||||
| chr13:36279331
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(36): Show | 52 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.315+4138T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36279331 | ||||||
| chr13:36279634
|
C | T | 1 | a0001c0001t0001g0005 | 5 | HG00738.hp2 HG01192.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+3835G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36279634 | ||||||
| chr13:36279668
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+3801T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36279668 | ||||||
| chr13:36279888
|
G | C | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315+3581C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36279888 | ||||||
| chr13:36279899
|
C | T | 1 | a0002c0003t0002g0144 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.315+3570G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36279899 | ||||||
| chr13:36280066
|
C | T | 8 | a0001c0001t0001g0046a0002c0003t0002g0017a0002c0003t0002g0018others(5): Show | 10 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.315+3403G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280066 | ||||||
| chr13:36280081
|
CATGA | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+3384_315+3387d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280081 | ||||||
| chr13:36280225
|
A | G | 170 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(167): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.315+3244T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280225 | ||||||
| chr13:36280425
|
A | T | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.315+3044T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280425 | ||||||
| chr13:36280535
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+2934G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280535 | ||||||
| chr13:36280536
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+2933T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280536 | ||||||
| chr13:36280611
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.315+2858T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280611 | ||||||
| chr13:36280691
|
C | A | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+2778G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280691 | ||||||
| chr13:36280775
|
T | C | 81 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(78): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.315+2694A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280775 | ||||||
| chr13:36280928
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+2541A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280928 | ||||||
| chr13:36280951
|
C | T | 1 | a0002c0002t0002g0230 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.315+2518G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36280951 | ||||||
| chr13:36281036
|
A | T | 85 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(82): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.315+2433T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281036 | ||||||
| chr13:36281107
|
G | A | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.315+2362C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281107 | ||||||
| chr13:36281147
|
G | A | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(25): Show | 42 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.315+2322C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281147 | ||||||
| chr13:36281238
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+2231G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281238 | ||||||
| chr13:36281268
|
A | G | 85 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(82): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.315+2201T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281268 | ||||||
| chr13:36281289
|
G | GA | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+2179dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281289 | ||||||
| chr13:36281332
|
G | A | 1 | a0001c0004t0001g0035 | 2 | NA18982.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.315+2137C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281332 | ||||||
| chr13:36281388
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.315+2081G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281388 | ||||||
| chr13:36281488
|
A | G | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.315+1981T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281488 | ||||||
| chr13:36281583
|
C | T | 2 | a0002c0003t0002g0040a0002c0003t0002g0051 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.315+1886G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281583 | ||||||
| chr13:36281606
|
T | C | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG01884.hp2 HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.315+1863A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281606 | ||||||
| chr13:36281627
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG02615.hp1 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.315+1842G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281627 | ||||||
| chr13:36281675
|
C | T | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+1794G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36281675 | ||||||
| chr13:36282126
|
ATGTC | A | 80 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0024others(77): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.315+1339_315+1342d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36282126 | ||||||
| chr13:36282131
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0177 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.315+1338A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36282131 | ||||||
| chr13:36282138
|
A | G | 2 | a0002c0002t0002g0223a0002c0002t0002g0224 | 2 | HG02735.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.315+1331T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36282138 | ||||||
| chr13:36282691
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.315+778C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36282691 | ||||||
| chr13:36282756
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.315+713T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36282756 | ||||||
| chr13:36282776
|
C | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+693G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36282776 | ||||||
| chr13:36282810
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.315+659A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36282810 | ||||||
| chr13:36282834
|
T | C | 170 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(167): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.315+635A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36282834 | ||||||
| chr13:36282974
|
A | C | 1 | a0002c0002t0002g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.315+495T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36282974 | ||||||
| chr13:36283076
|
C | G | 6 | a0001c0001t0001g0029a0001c0001t0001g0103a0001c0001t0001g0116others(3): Show | 7 | HG01884.hp1 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.315+393G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36283076 | ||||||
| chr13:36283145
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0171 | 2 | HG02074.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.315+324C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36283145 | ||||||
| chr13:36283153
|
G | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+316C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36283153 | ||||||
| chr13:36283218
|
G | A | 1 | a0002c0002t0002g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.315+251C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36283218 | ||||||
| chr13:36283240
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0097 | 6 | HG00738.hp2 HG01192.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+229T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36283240 | ||||||
| chr13:36283292
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.315+177A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36283292 | ||||||
| chr13:36283331
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+138G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36283331 | ||||||
| chr13:36283342
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+127T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36283342 | ||||||
| chr13:36283363
|
A | C | 84 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(81): Show | 105 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.315+106T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36283363 | ||||||
| chr13:36283377
|
C | T | 1 | a0002c0002t0002g0238 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.315+92G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36283377 | ||||||
| chr13:36283575
|
T | C | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.274+17A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 3/7 | chr13 | 36283575 | ||||||
| chr13:36283753
|
T | C | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.164-51A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36283753 | ||||||
| chr13:36283879
|
C | T | 67 | a0001c0004t0001g0240a0001c0004t0001g0274a0001c0004t0001g0293others(64): Show | 82 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.164-177G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36283879 | ||||||
| chr13:36284035
|
C | A | 1 | a0001c0001t0001g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.164-333G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36284035 | ||||||
| chr13:36284115
|
ATATATAT others(32): Show |
A | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.164-452_164-414del others(39): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36284115 | ||||||
| chr13:36284386
|
C | T | 1 | a0002c0002t0002g0227 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.164-684G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36284386 | ||||||
| chr13:36284401
|
TC | T | 84 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(81): Show | 105 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.164-700delG | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36284401 | ||||||
| chr13:36284452
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0177 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.164-750C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36284452 | ||||||
| chr13:36284785
|
A | G | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.164-1083T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36284785 | ||||||
| chr13:36284913
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164-1211T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36284913 | ||||||
| chr13:36285323
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(280): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.164-1621A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285323 | ||||||
| chr13:36285377
|
C | T | 3 | a0002c0002t0002g0269a0002c0002t0002g0270a0002c0002t0002g0271 | 3 | HG02523.hp2 NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.164-1675G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285377 | ||||||
| chr13:36285451
|
G | C | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-1749C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285451 | ||||||
| chr13:36285584
|
A | AAGAT | 26 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(23): Show | 38 | HG00323.hp1 HG00738.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.164-1886_164-1883d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285584 | ||||||
| chr13:36285584
|
A | AAGATAGA others(1): Show |
24 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0029others(21): Show | 30 | HG00280.hp2 HG00621.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.164-1890_164-1883d others(10): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285584 | ||||||
| chr13:36285584
|
A | AAGATAGA others(5): Show |
18 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0028others(15): Show | 24 | HG00735.hp1 HG01070.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.164-1894_164-1883d others(14): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285584 | ||||||
| chr13:36285584
|
A | AAGATAGA others(9): Show |
8 | a0001c0001t0001g0027a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 9 | HG00733.hp2 HG01074.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-1898_164-1883d others(18): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285584 | ||||||
| chr13:36285584
|
A | AAGATAGA others(13): Show |
1 | a0003c0006t0002g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.164-1902_164-1883d others(22): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285584 | ||||||
| chr13:36285584
|
AAGATAGA others(5): Show |
A | 1 | a0001c0001t0001g0129 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.164-1894_164-1883d others(14): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285584 | ||||||
| chr13:36285603
|
A | ATAGATAG others(25): Show |
3 | a0002c0003t0002g0016a0002c0003t0002g0038a0002c0003t0002g0185 | 4 | HG02602.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-1902_164-1901i others(34): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285603 | ||||||
| chr13:36285603
|
A | ATAGATAG others(21): Show |
1 | a0002c0003t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.164-1902_164-1901i others(30): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285603 | ||||||
| chr13:36285603
|
A | ATAGATAG others(17): Show |
5 | a0002c0003t0002g0040a0002c0003t0002g0041a0002c0003t0002g0042others(2): Show | 5 | HG00280.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-1902_164-1901i others(26): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285603 | ||||||
| chr13:36285603
|
A | ATAGATAG others(13): Show |
11 | a0001c0001t0001g0046a0002c0003t0002g0017a0002c0003t0002g0018others(8): Show | 13 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.164-1902_164-1901i others(22): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285603 | ||||||
| chr13:36285603
|
A | ATAGATAG others(5): Show |
3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG02615.hp1 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.164-1902_164-1901i others(14): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285603 | ||||||
| chr13:36285606
|
G | GATAGATA others(9): Show |
1 | a0001c0001t0001g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.164-1905_164-1904i others(18): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285606 | ||||||
| chr13:36285614
|
G | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0102a0001c0001t0001g0153others(2): Show | 5 | HG02040.hp2 HG02071.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-1912C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285614
|
G | GATAC | 37 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(34): Show | 47 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.164-1913_164-1912i others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285614
|
G | GATAGATA others(1): Show |
4 | a0001c0007t0001g0068a0002c0003t0002g0174a0002c0003t0002g0175others(1): Show | 4 | HG00423.hp2 HG00621.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-1920_164-1913d others(10): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285614
|
G | GATAGATA others(9): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 5 | HG00140.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-1928_164-1913d others(18): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285614
|
G | GATAGATA others(17): Show |
1 | a0001c0001t0001g0097 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.164-1936_164-1913d others(26): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285614
|
G | GATAGATA others(5): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 5 | HG02015.hp1 HG03041.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-1913_164-1912i others(14): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285614
|
G | GATAGATA others(13): Show |
1 | a0001c0001t0001g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.164-1913_164-1912i others(22): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285614
|
G | GATAGATA others(9): Show |
25 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0024others(22): Show | 29 | HG01106.hp1 HG01168.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.164-1913_164-1912i others(18): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285614
|
G | GATAGATA others(17): Show |
1 | a0001c0001t0001g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164-1913_164-1912i others(26): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285614
|
G | GATAGATA others(13): Show |
9 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(6): Show | 9 | HG00597.hp2 HG01123.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-1913_164-1912i others(22): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285614
|
G | GATAGATA others(17): Show |
1 | a0002c0002t0002g0227 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.164-1913_164-1912i others(26): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285614 | ||||||
| chr13:36285618
|
G | C | 2 | a0001c0004t0001g0293a0004c0008t0003g0288 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.164-1916C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285618 | ||||||
| chr13:36285618
|
G | GATACATA others(5): Show |
1 | a0002c0002t0003g0289 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.164-1917_164-1916i others(14): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285618 | ||||||
| chr13:36285618
|
G | GATAGATA others(1): Show |
11 | a0001c0004t0001g0009a0001c0004t0001g0274a0001c0004t0001g0276others(8): Show | 15 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.164-1917_164-1916i others(10): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285618 | ||||||
| chr13:36285618
|
G | GATAGATA others(5): Show |
6 | a0001c0004t0001g0280a0002c0002t0002g0278a0002c0002t0002g0279others(3): Show | 6 | HG01069.hp1 HG01123.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-1917_164-1916i others(14): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285618 | ||||||
| chr13:36285618
|
G | GATAGATA others(5): Show |
50 | a0001c0004t0001g0015a0001c0004t0001g0035a0001c0004t0001g0221others(47): Show | 66 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.164-1917_164-1916i others(14): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285618 | ||||||
| chr13:36285618
|
G | GATAGATA others(9): Show |
1 | a0002c0002t0002g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.164-1917_164-1916i others(18): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285618 | ||||||
| chr13:36285618
|
G | GATAGATA others(9): Show |
11 | a0001c0004t0001g0237a0002c0002t0002g0030a0002c0002t0002g0222others(8): Show | 12 | HG01981.hp2 HG02004.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.164-1917_164-1916i others(18): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285618 | ||||||
| chr13:36285618
|
G | GATAGATA others(13): Show |
1 | a0002c0002t0002g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.164-1917_164-1916i others(22): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285618 | ||||||
| chr13:36285618
|
G | GATAGATA others(13): Show |
4 | a0001c0004t0001g0225a0002c0002t0002g0228a0002c0002t0002g0229others(1): Show | 4 | NA18943.hp1 NA19054.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-1917_164-1916i others(22): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285618 | ||||||
| chr13:36285618
|
GATAC | G | 2 | a0001c0001t0001g0133a0002c0003t0003g0010 | 4 | HG03130.hp1 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-1920_164-1917d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285618 | ||||||
| chr13:36285622
|
C | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 8 | HG00609.hp2 HG01516.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-1920G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285622 | ||||||
| chr13:36285630
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.164-1928G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285630 | ||||||
| chr13:36285654
|
G | C | 2 | a0002c0002t0002g0281a0002c0002t0002g0282 | 2 | HG01257.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.164-1952C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285654 | ||||||
| chr13:36285699
|
G | A | 1 | a0002c0002t0002g0283 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.164-1997C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285699 | ||||||
| chr13:36285873
|
T | G | 1 | a0001c0001t0001g0098 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.164-2171A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36285873 | ||||||
| chr13:36286437
|
A | G | 1 | a0002c0003t0003g0010 | 3 | HG03130.hp1 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.164-2735T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36286437 | ||||||
| chr13:36286506
|
T | C | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.164-2804A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36286506 | ||||||
| chr13:36286774
|
C | A | 1 | a0002c0003t0002g0144 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.164-3072G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36286774 | ||||||
| chr13:36286840
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.164-3138G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36286840 | ||||||
| chr13:36287086
|
C | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 6 | HG01109.hp1 HG01167.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-3384G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36287086 | ||||||
| chr13:36287134
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.164-3432T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36287134 | ||||||
| chr13:36287162
|
ATCTTCCC | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.164-3467_164-3461d others(9): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36287162 | ||||||
| chr13:36287290
|
T | A | 169 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0024others(166): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.164-3588A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36287290 | ||||||
| chr13:36287518
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.164-3816G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36287518 | ||||||
| chr13:36287936
|
T | C | 45 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(42): Show | 55 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.164-4234A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36287936 | ||||||
| chr13:36288038
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.164-4336A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36288038 | ||||||
| chr13:36288086
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.164-4384C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36288086 | ||||||
| chr13:36288153
|
C | T | 2 | a0001c0001t0001g0067a0001c0004t0001g0293 | 2 | HG01099.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.164-4451G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36288153 | ||||||
| chr13:36288236
|
G | A | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-4534C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36288236 | ||||||
| chr13:36288256
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.164-4554G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36288256 | ||||||
| chr13:36288257
|
G | A | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.164-4555C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36288257 | ||||||
| chr13:36288315
|
G | A | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.164-4613C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36288315 | ||||||
| chr13:36288399
|
G | C | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.164-4697C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36288399 | ||||||
| chr13:36288424
|
T | C | 28 | a0001c0001t0001g0046a0001c0001t0001g0182a0001c0001t0001g0183others(25): Show | 31 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.164-4722A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36288424 | ||||||
| chr13:36288599
|
C | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.164-4897G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36288599 | ||||||
| chr13:36289042
|
C | T | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-5340G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289042 | ||||||
| chr13:36289199
|
T | C | 25 | a0001c0001t0001g0046a0002c0003t0002g0016a0002c0003t0002g0017others(22): Show | 28 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-5497A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289199 | ||||||
| chr13:36289263
|
G | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.164-5561C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289263 | ||||||
| chr13:36289287
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.164-5585G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289287 | ||||||
| chr13:36289296
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.164-5594G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289296 | ||||||
| chr13:36289347
|
G | C | 1 | a0001c0001t0004g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.164-5645C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289347 | ||||||
| chr13:36289479
|
T | C | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-5777A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289479 | ||||||
| chr13:36289504
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.164-5802A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289504 | ||||||
| chr13:36289520
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164-5818T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289520 | ||||||
| chr13:36289527
|
A | G | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.164-5825T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289527 | ||||||
| chr13:36289581
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.164-5879G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289581 | ||||||
| chr13:36289724
|
T | A | 81 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(78): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.164-6022A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289724 | ||||||
| chr13:36289738
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00558.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.164-6036A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289738 | ||||||
| chr13:36289994
|
A | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(289): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.163+5784T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289994 | ||||||
| chr13:36290232
|
G | A | 2 | a0002c0002t0002g0223a0002c0002t0002g0224 | 2 | HG02735.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.163+5546C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36290232 | ||||||
| chr13:36290239
|
C | T | 1 | a0001c0004t0001g0225 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.163+5539G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36290239 | ||||||
| chr13:36290412
|
T | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(31): Show | 46 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.163+5366A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36290412 | ||||||
| chr13:36290530
|
A | C | 2 | a0001c0004t0001g0293a0004c0008t0003g0288 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.163+5248T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36290530 | ||||||
| chr13:36290560
|
G | A | 81 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(78): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.163+5218C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36290560 | ||||||
| chr13:36290944
|
C | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+4834G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36290944 | ||||||
| chr13:36290984
|
TA | T | 86 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(83): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.163+4793delT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36290984 | ||||||
| chr13:36291078
|
G | A | 87 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(84): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.163+4700C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291078 | ||||||
| chr13:36291122
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+4656A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291122 | ||||||
| chr13:36291139
|
T | C | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+4639A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291139 | ||||||
| chr13:36291227
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.163+4551A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291227 | ||||||
| chr13:36291240
|
A | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 51 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.163+4538T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291240 | ||||||
| chr13:36291299
|
T | C | 170 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(167): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.163+4479A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291299 | ||||||
| chr13:36291309
|
TAG | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+4467_163+4468d others(4): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291309 | ||||||
| chr13:36291371
|
C | T | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+4407G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291371 | ||||||
| chr13:36291455
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.163+4323G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291455 | ||||||
| chr13:36291987
|
T | G | 1 | a0004c0008t0003g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163+3791A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291987 | ||||||
| chr13:36291989
|
C | CT | 40 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(37): Show | 50 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.163+3788dupA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291989 | ||||||
| chr13:36291989
|
CT | C | 90 | a0001c0001t0001g0207a0001c0004t0001g0009a0001c0004t0001g0015others(87): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.163+3788delA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36291989 | ||||||
| chr13:36292038
|
G | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+3740C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36292038 | ||||||
| chr13:36292090
|
C | T | 1 | a0002c0002t0002g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.163+3688G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36292090 | ||||||
| chr13:36292219
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+3559A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36292219 | ||||||
| chr13:36292241
|
G | A | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+3537C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36292241 | ||||||
| chr13:36292289
|
T | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+3489A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36292289 | ||||||
| chr13:36292594
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.163+3184G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36292594 | ||||||
| chr13:36292601
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): Show | 269 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.163+3177G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36292601 | ||||||
| chr13:36292814
|
A | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | NA19009.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.163+2964T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36292814 | ||||||
| chr13:36293105
|
GAAGA | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 95 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.163+2669_163+2672d others(6): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36293105 | ||||||
| chr13:36293383
|
C | T | 1 | a0002c0002t0002g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.163+2395G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36293383 | ||||||
| chr13:36293682
|
A | G | 87 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(84): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.163+2096T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36293682 | ||||||
| chr13:36293945
|
A | T | 1 | a0002c0003t0002g0037 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+1833T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36293945 | ||||||
| chr13:36294033
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.163+1745C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294033 | ||||||
| chr13:36294072
|
A | G | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.163+1706T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294072 | ||||||
| chr13:36294214
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.163+1564G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294214 | ||||||
| chr13:36294220
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.163+1558G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294220 | ||||||
| chr13:36294221
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.163+1557A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294221 | ||||||
| chr13:36294317
|
T | C | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.163+1461A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294317 | ||||||
| chr13:36294357
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.163+1421A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294357 | ||||||
| chr13:36294359
|
C | A | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.163+1419G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294359 | ||||||
| chr13:36294360
|
T | G | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.163+1418A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294360 | ||||||
| chr13:36294757
|
A | T | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+1021T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294757 | ||||||
| chr13:36294807
|
G | C | 2 | a0002c0002t0003g0217a0002c0002t0003g0289 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.163+971C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294807 | ||||||
| chr13:36294849
|
A | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(47): Show | 60 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.163+929T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294849 | ||||||
| chr13:36294899
|
A | G | 85 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(82): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.163+879T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36294899 | ||||||
| chr13:36295136
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0137others(7): Show | 11 | HG01106.hp1 HG01123.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+642G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36295136 | ||||||
| chr13:36295303
|
G | A | 1 | a0002c0002t0002g0291 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.163+475C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36295303 | ||||||
| chr13:36295438
|
T | C | 85 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(82): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.163+340A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36295438 | ||||||
| chr13:36295706
|
G | C | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+72C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36295706 | ||||||
| chr13:36295892
|
A | C | 8 | a0001c0005t0001g0058a0001c0005t0001g0059a0001c0005t0001g0060others(5): Show | 8 | HG01106.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-35T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36295892 | ||||||
| chr13:36296003
|
A | AT | 87 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(84): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.84-147_84-146insA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296003 | ||||||
| chr13:36296100
|
T | C | 81 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(78): Show | 94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.84-243A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296100 | ||||||
| chr13:36296219
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.84-362T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296219 | ||||||
| chr13:36296283
|
A | G | 89 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(86): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.84-426T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296283 | ||||||
| chr13:36296427
|
C | T | 1 | a0001c0001t0001g0057 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.84-570G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296427 | ||||||
| chr13:36296701
|
A | G | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-844T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296701 | ||||||
| chr13:36296704
|
T | A | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-847A>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296704 | ||||||
| chr13:36296704
|
T | C | 1 | a0002c0002t0003g0289 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.84-847A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296704 | ||||||
| chr13:36296705
|
A | C | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-848T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296705 | ||||||
| chr13:36296707
|
C | G | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-850G>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296707 | ||||||
| chr13:36296708
|
A | C | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-851T>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296708 | ||||||
| chr13:36296710
|
T | C | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-853A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296710 | ||||||
| chr13:36296713
|
C | T | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-856G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296713 | ||||||
| chr13:36296714
|
G | C | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-857C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296714 | ||||||
| chr13:36296715
|
G | C | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-858C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296715 | ||||||
| chr13:36296716
|
C | A | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-859G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296716 | ||||||
| chr13:36296720
|
A | G | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-863T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296720 | ||||||
| chr13:36296725
|
T | C | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-868A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296725 | ||||||
| chr13:36296727
|
C | A | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-870G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296727 | ||||||
| chr13:36296728
|
A | G | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84-871T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296728 | ||||||
| chr13:36296748
|
C | A | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.83+889G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296748 | ||||||
| chr13:36296749
|
A | T | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.83+888T>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296749 | ||||||
| chr13:36296751
|
T | C | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.83+886A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296751 | ||||||
| chr13:36296753
|
CTAAGTTC others(4): Show |
C | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.83+873_83+883delTA others(9): Show |
CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296753 | ||||||
| chr13:36296765
|
T | C | 88 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(85): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.83+872A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296765 | ||||||
| chr13:36296812
|
G | T | 1 | a0002c0002t0003g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.83+825C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296812 | ||||||
| chr13:36296927
|
G | A | 1 | a0002c0003t0002g0052 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.83+710C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296927 | ||||||
| chr13:36296946
|
C | A | 3 | a0002c0003t0002g0053a0002c0003t0002g0054a0002c0003t0002g0055 | 3 | HG02896.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.83+691G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296946 | ||||||
| chr13:36296967
|
G | C | 1 | a0002c0002t0002g0290 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.83+670C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36296967 | ||||||
| chr13:36297007
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.83+630T>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36297007 | ||||||
| chr13:36297174
|
C | T | 1 | a0002c0002t0002g0291 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.83+463G>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36297174 | ||||||
| chr13:36297276
|
C | A | 2 | a0002c0002t0002g0291a0002c0002t0002g0292 | 2 | NA18943.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.83+361G>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36297276 | ||||||
| chr13:36297321
|
T | G | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.83+316A>C | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36297321 | ||||||
| chr13:36297425
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(24): Show | 39 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.83+212C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36297425 | ||||||
| chr13:36297425
|
G | C | 88 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(85): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.83+212C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36297425 | ||||||
| chr13:36297436
|
T | C | 88 | a0001c0004t0001g0009a0001c0004t0001g0015a0001c0004t0001g0035others(85): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.83+201A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36297436 | ||||||
| chr13:36297593
|
G | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0210a0001c0001t0001g0211 | 4 | HG02280.hp2 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+44C>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36297593 | ||||||
| chr13:36297593
|
G | T | 22 | a0001c0001t0001g0046a0002c0003t0002g0016a0002c0003t0002g0017others(19): Show | 25 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.83+44C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36297593 | ||||||
| chr13:36297627
|
G | A | 93 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(90): Show | 114 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.83+10C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 1/7 | chr13 | 36297627 |