Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 214 | 240 | 65 | 36 | 108 | 8 | 21 | 85 | CCDC169_chr13_36225775_36302814 | CCDC169 | MKEER others(209): Show |
chr13 | 36225775 | 36302814 |
| a0002 | 0/0 | 214 | 121 | 18 | 26 | 50 | 6 | 21 | 35 | CCDC169_chr13_36225775_36302814 | CCDC169 | MKEER others(209): Show |
chr13 | 36225775 | 36302814 |
| a0003 | 0/0 | 214 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | MKEER others(209): Show |
chr13 | 36225775 | 36302814 |
| a0004 | 0/0 | 214 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | MKEER others(209): Show |
chr13 | 36225775 | 36302814 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 642 | 208 | 57 | 32 | 89 | 8 | 20 | CCDC169_chr13_36225775_36302814 | CCDC169 | ATGAA others(637): Show |
chr13 | 36225775 | 36302814 | ||
| a0001c0004 | 0/0 | 642 | 23 | 1 | 3 | 18 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | ATGAA others(637): Show |
chr13 | 36225775 | 36302814 | ||
| a0001c0005 | 0/0 | 642 | 8 | 7 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ATGAA others(637): Show |
chr13 | 36225775 | 36302814 | ||
| a0001c0007 | 0/0 | 642 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ATGAA others(637): Show |
chr13 | 36225775 | 36302814 | ||
| a0002c0002 | 0/0 | 642 | 86 | 8 | 16 | 46 | 4 | 12 | CCDC169_chr13_36225775_36302814 | CCDC169 | ATGAA others(637): Show |
chr13 | 36225775 | 36302814 | ||
| a0002c0003 | 0/0 | 642 | 35 | 10 | 10 | 4 | 2 | 9 | CCDC169_chr13_36225775_36302814 | CCDC169 | ATGAA others(637): Show |
chr13 | 36225775 | 36302814 | ||
| a0003c0006 | 0/0 | 642 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ATGAA others(637): Show |
chr13 | 36225775 | 36302814 | ||
| a0004c0008 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ATGAA others(637): Show |
chr13 | 36225775 | 36302814 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1158 | 207 | 56 | 32 | 89 | 8 | 20 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1153): Show |
chr13 | 36225775 | 36302814 |
| a0001c0001t0004 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1153): Show |
chr13 | 36225775 | 36302814 |
| a0001c0004t0001 | 0/0 | 1158 | 23 | 1 | 3 | 18 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1153): Show |
chr13 | 36225775 | 36302814 |
| a0001c0005t0001 | 0/0 | 1158 | 8 | 7 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1153): Show |
chr13 | 36225775 | 36302814 |
| a0001c0007t0001 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1153): Show |
chr13 | 36225775 | 36302814 |
| a0002c0002t0002 | 0/0 | 1157 | 83 | 6 | 16 | 45 | 4 | 12 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1152): Show |
chr13 | 36225775 | 36302814 |
| a0002c0002t0003 | 0/0 | 1158 | 3 | 2 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1153): Show |
chr13 | 36225775 | 36302814 |
| a0002c0003t0002 | 0/0 | 1157 | 32 | 7 | 10 | 4 | 2 | 9 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1152): Show |
chr13 | 36225775 | 36302814 |
| a0002c0003t0003 | 0/0 | 1158 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1153): Show |
chr13 | 36225775 | 36302814 |
| a0003c0006t0002 | 0/0 | 1157 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1152): Show |
chr13 | 36225775 | 36302814 |
| a0004c0008t0003 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | ACCGC others(1153): Show |
chr13 | 36225775 | 36302814 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0002 | 0/0 | 6 | 4 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0005 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0007 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0005t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0001c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0006 | 0/0 | 5 | 0 | 0 | 1 | 2 | 2 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0002t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0018 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0002c0003t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0003c0006t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0003c0006t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| a0004c0008t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0247 | EUR | GBR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0018 | EUR | GBR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0227 | EUR | GBR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00280 | hp1 | a0002 | c0003 | t0002 | g0042 | EUR | FIN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | FIN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0292 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00423 | hp2 | a0002 | c0003 | t0002 | g0175 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00621 | hp1 | a0002 | c0003 | t0002 | g0174 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00639 | hp1 | a0002 | c0003 | t0002 | g0047 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0279 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0274 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | CHS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00733 | hp1 | a0002 | c0003 | t0002 | g0048 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0277 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00738 | hp1 | a0002 | c0003 | t0002 | g0045 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0280 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01069 | hp2 | a0002 | c0003 | t0002 | g0017 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0044 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0285 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01106 | hp2 | a0001 | c0005 | t0001 | g0062 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01167 | hp2 | a0002 | c0003 | t0002 | g0051 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01169 | hp2 | a0002 | c0003 | t0002 | g0040 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01175 | hp1 | a0002 | c0003 | t0002 | g0052 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0245 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0259 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0284 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0043 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0255 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | IBS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01981 | hp1 | a0001 | c0004 | t0001 | g0266 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0030 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01993 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01993 | hp2 | a0002 | c0003 | t0002 | g0144 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0237 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0015 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0249 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0242 | EAS | CDX | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | CDX | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02257 | hp1 | a0002 | c0002 | t0003 | g0291 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02257 | hp2 | a0003 | c0006 | t0002 | g0050 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02280 | hp1 | a0002 | c0002 | t0003 | g0218 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02300 | hp1 | a0001 | c0004 | t0001 | g0222 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02523 | hp1 | a0002 | c0003 | t0002 | g0190 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | KHV | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02602 | hp2 | a0002 | c0003 | t0002 | g0038 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0221 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0061 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0223 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0059 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02683 | hp1 | a0002 | c0003 | t0002 | g0039 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02723 | hp2 | a0004 | c0008 | t0003 | g0290 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0225 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0275 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02738 | hp2 | a0001 | c0004 | t0001 | g0276 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0246 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02896 | hp1 | a0002 | c0003 | t0002 | g0053 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02897 | hp2 | a0002 | c0003 | t0002 | g0054 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0293 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02976 | hp2 | a0001 | c0005 | t0001 | g0065 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03041 | hp2 | a0002 | c0003 | t0002 | g0187 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0220 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0063 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03130 | hp1 | a0002 | c0003 | t0003 | g0010 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03139 | hp2 | a0002 | c0003 | t0002 | g0055 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0060 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0263 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03669 | hp1 | a0002 | c0003 | t0002 | g0075 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03669 | hp2 | a0002 | c0003 | t0002 | g0037 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0224 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03704 | hp1 | a0002 | c0003 | t0002 | g0164 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03704 | hp2 | a0002 | c0003 | t0002 | g0016 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03834 | hp2 | a0002 | c0003 | t0002 | g0185 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0264 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG04115 | hp1 | a0002 | c0003 | t0002 | g0017 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0244 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0016 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18612 | hp1 | a0001 | c0004 | t0001 | g0267 | EAS | CHB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0058 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0239 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18946 | hp2 | a0001 | c0004 | t0001 | g0268 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18954 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18971 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18981 | hp2 | a0001 | c0007 | t0001 | g0068 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18982 | hp2 | a0001 | c0004 | t0001 | g0035 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0278 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18988 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18989 | hp1 | a0001 | c0004 | t0001 | g0035 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18999 | hp1 | a0001 | c0004 | t0001 | g0287 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19002 | hp1 | a0001 | c0004 | t0001 | g0260 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0064 | AFR | LWK | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19057 | hp2 | a0002 | c0003 | t0002 | g0176 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0226 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19067 | hp1 | a0001 | c0004 | t0001 | g0261 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19085 | hp2 | a0001 | c0004 | t0001 | g0282 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19086 | hp2 | a0002 | c0002 | t0003 | g0251 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0234 | AFR | YRI | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ASW | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | TSI | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | GIH | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0265 | SAS | GIH | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0281 | AMR | CLM | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG02559 | hp2 | a0003 | c0006 | t0002 | g0049 | AFR | ACB | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03471 | hp1 | a0002 | c0003 | t0002 | g0186 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG03471 | hp2 | a0002 | c0003 | t0003 | g0010 | AFR | MSL | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | USA | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| HG06807 | hp2 | a0002 | c0003 | t0002 | g0041 | AFR | USA | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA20300 | hp1 | a0002 | c0003 | t0003 | g0010 | AFR | USA | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| NA20300 | hp2 | a0002 | c0003 | t0002 | g0018 | AFR | USA | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0057 | REF | REF | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0134 | REF | REF | CCDC169_chr13_36225775_36302814 | CCDC169 | chr13 | 36225775 | 36302814 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0002 a0003 a0004 |
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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0004 a0002c0002 a0004c0008 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:36231029 | T | C | 6 | a0002c0002t0002 a0002c0002t0003 a0002c0003t0002 others(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 | a0002c0002t0002 a0002c0003t0002 a0003c0006t0002 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
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 | 43 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(40): Show |
52 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(49): 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
237 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(234): 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0288 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0191 a0001c0001t0001g0197 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0288 a0002c0002t0002g0289 a0002c0003t0002g0174 others(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 | a0002c0002t0002g0288 a0002c0002t0002g0289 a0002c0003t0002g0174 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0264 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
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 | a0002c0003t0003g0010 a0004c0008t0003g0290 |
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 | a0002c0003t0003g0010 a0004c0008t0003g0290 |
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 | a0002c0002t0002g0224 a0002c0002t0002g0225 a0002c0003t0002g0075 |
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 | a0002c0003t0003g0010 a0004c0008t0003g0290 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0249 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0005t0001g0058 a0001c0005t0001g0059 a0001c0005t0001g0060 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0152 a0001c0001t0001g0153 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0005t0001g0058 a0001c0005t0001g0059 a0001c0005t0001g0060 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | 17 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0056 others(14): Show |
19 | HG00140.hp2 HG01106.hp1 HG01123.hp1 others(16): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0002c0003t0002g0044 a0002c0003t0002g0045 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0004c0008t0003g0290 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0005t0001g0058 a0001c0005t0001g0059 a0001c0005t0001g0060 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
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 | a0001c0001t0001g0147 a0001c0001t0001g0156 a0001c0001t0001g0166 |
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 | a0002c0003t0003g0010 a0004c0008t0003g0290 |
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 | 38 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(35): Show |
47 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(44): 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 | a0002c0003t0003g0010 a0004c0008t0003g0290 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0074 a0001c0004t0001g0276 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0231 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0002c0003t0002g0016 a0002c0003t0002g0017 a0002c0003t0002g0018 others(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 | 72 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(69): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): 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 | a0001c0001t0001g0029 a0001c0001t0001g0103 a0001c0001t0001g0135 others(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 | a0002c0003t0003g0010 a0004c0008t0003g0290 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0005t0001g0058 a0001c0005t0001g0059 a0001c0005t0001g0060 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0253 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0029 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0269 | 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 | a0002c0002t0002g0259 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | |||||||
| chr13:36246673 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0152 a0001c0001t0001g0153 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | 43 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(40): Show |
52 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(49): 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0005t0001g0058 a0001c0005t0001g0059 a0001c0005t0001g0060 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0002c0002t0002g0221 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
237 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.469-221dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36248902 | |||||||
| chr13:36248999 | G | T | 104 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0003t0002g0016 a0002c0003t0002g0017 a0002c0003t0002g0018 others(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 | a0001c0001t0001g0097 a0002c0002t0002g0003 a0002c0002t0002g0006 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0031 a0002c0002t0002g0033 others(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 | a0002c0002t0002g0271 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | 49 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(46): Show |
58 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.469-820C>T | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36249502 | |||||||
| chr13:36249594 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(46): Show |
58 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(55): 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | 41 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(38): Show |
50 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(47): 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(287): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): 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 | a0002c0002t0002g0244 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0066 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0003g0291 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | |||||||
| chr13:36252097 | 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 | a0001c0005t0001g0062 a0001c0005t0001g0064 |
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 | 155 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(152): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): 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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0002c0002t0002g0248 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0292 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | 50 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(47): Show |
59 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.468+474A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 6/7 | chr13 | 36253329 | |||||||
| chr13:36253340 | CT | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(186): Show |
242 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(239): 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 | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(184): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0224 a0002c0002t0002g0225 a0002c0003t0002g0075 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0220 a0002c0003t0002g0016 a0002c0003t0002g0017 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0217 a0002c0002t0002g0219 a0002c0002t0002g0235 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0087 a0001c0001t0001g0100 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(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 | a0002c0002t0002g0236 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0003t0003g0010 a0004c0008t0003g0290 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0243 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0066 a0001c0001t0001g0069 others(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 | |||||||
| chr13:36255557 | C | G | 104 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(71): Show |
92 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.316-1517dupT | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36255659 | |||||||
| chr13:36255659 | T | TAAAA | 28 | a0002c0002t0002g0220 a0002c0002t0002g0230 a0002c0002t0002g0257 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0032 a0002c0002t0002g0224 a0002c0002t0002g0225 others(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 | a0002c0002t0002g0220 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0280 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0264 a0002c0002t0002g0269 a0002c0002t0002g0292 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0278 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0269 | 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 | a0002c0002t0002g0256 | 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 | a0002c0003t0002g0016 a0002c0003t0002g0017 a0002c0003t0002g0018 others(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 | a0002c0002t0002g0033 a0002c0002t0002g0229 a0002c0002t0002g0230 others(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 | 50 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(47): Show |
59 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(56): 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 | a0001c0001t0001g0150 a0001c0001t0001g0177 |
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 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0220 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | |||||||
| chr13:36257160 | T | G | 2 | a0002c0003t0003g0010 a0004c0008t0003g0290 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | |||||||
| chr13:36257516 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0230 a0002c0003t0002g0176 a0002c0003t0003g0010 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0161 a0002c0002t0002g0034 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0110 a0001c0001t0001g0195 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0005t0001g0058 a0001c0005t0001g0059 a0001c0005t0001g0060 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0002c0002t0002g0224 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0003t0002g0016 a0002c0003t0002g0039 a0002c0003t0002g0185 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0098 |
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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0046 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0002c0002t0002g0262 a0002c0002t0002g0270 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0003t0003g0010 a0004c0008t0003g0290 |
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 | a0002c0002t0002g0286 | 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 | a0002c0002t0003g0291 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0004t0001g0267 | 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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0255 | 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 | a0001c0001t0001g0147 a0001c0001t0001g0156 a0001c0001t0001g0166 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
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 | a0001c0004t0001g0278 | 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 | 36 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0025 others(33): Show |
41 | HG00140.hp2 HG00597.hp2 HG01106.hp1 others(38): 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 | a0002c0003t0003g0010 a0004c0008t0003g0290 |
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 | a0002c0002t0002g0003 a0002c0002t0002g0006 a0002c0002t0002g0030 others(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 | 34 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0025 others(31): Show |
39 | HG00140.hp2 HG01106.hp1 HG01123.hp1 others(36): 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 | a0001c0001t0001g0014 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0070 others(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 | a0002c0002t0003g0218 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0026 others(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 | a0002c0002t0002g0224 | 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 | a0001c0001t0001g0108 a0001c0004t0001g0009 a0001c0004t0001g0015 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0274 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | |||||||
| chr13:36265143 | C | A | 1 | a0004c0008t0003g0290 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0256 | 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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | 79 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(76): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): 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 | a0001c0001t0001g0076 a0001c0001t0001g0101 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0215 a0001c0004t0001g0009 a0001c0004t0001g0015 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0293 a0004c0008t0003g0290 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0247 a0002c0002t0002g0274 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | 78 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0024 others(75): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0074 a0001c0004t0001g0009 a0001c0004t0001g0015 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0002c0002t0002g0228 | 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 | a0001c0004t0001g0266 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0107 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0221 a0002c0002t0002g0234 a0002c0002t0002g0246 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0177 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0219 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0003t0002g0044 a0002c0003t0002g0045 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0220 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0002c0003t0002g0053 a0002c0003t0002g0054 a0002c0003t0002g0055 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0223 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0139 a0001c0001t0001g0140 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0003t0002g0040 a0002c0003t0002g0048 a0002c0003t0002g0051 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0004t0001g0009 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0004c0008t0003g0290 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(173): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(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 | a0002c0003t0002g0016 a0002c0003t0002g0038 a0002c0003t0002g0039 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0223 | 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 | a0002c0002t0002g0217 a0002c0002t0002g0231 |
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 | a0002c0002t0002g0220 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0263 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0004c0008t0003g0290 | 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 | a0002c0002t0002g0259 | 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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(104): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.315+8600dupA | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36274868 | |||||||
| chr13:36274868 | A | ATT | 43 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0111 a0001c0004t0001g0009 others(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 | a0001c0004t0001g0242 a0001c0004t0001g0260 a0001c0004t0001g0261 others(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 | a0001c0001t0001g0194 a0001c0005t0001g0059 a0001c0005t0001g0060 others(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 | |||||||
| chr13:36274959 | 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 | a0004c0008t0003g0290 | 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 | a0001c0001t0001g0204 a0001c0004t0001g0009 a0001c0004t0001g0015 others(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 | a0001c0004t0001g0293 a0001c0005t0001g0060 a0001c0005t0001g0065 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0004c0008t0003g0290 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0241 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0003g0291 | 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 | a0002c0003t0002g0016 a0002c0003t0002g0039 a0002c0003t0002g0185 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0001c0001t0001g0127 a0001c0001t0001g0212 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0071 a0001c0001t0001g0102 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
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 | a0004c0008t0003g0290 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+5011C>A | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 4/7 | chr13 | 36278458 | |||||||
| chr13:36278800 | G | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0046 a0002c0003t0002g0017 a0002c0003t0002g0018 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | 169 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(166): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0004c0008t0003g0290 | 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 | 80 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(77): Show |
93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0232 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0002c0003t0002g0040 a0002c0003t0002g0051 |
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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
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 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0004c0008t0003g0290 | 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 | 79 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0024 others(76): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): 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 | a0001c0001t0001g0150 a0001c0001t0001g0177 |
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 | a0002c0002t0002g0224 a0002c0002t0002g0225 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | 169 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(166): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): 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 | a0002c0002t0002g0259 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0103 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0171 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0259 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0097 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0240 | 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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | a0001c0004t0001g0242 a0001c0004t0001g0276 a0001c0004t0001g0293 others(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 | a0002c0002t0002g0228 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0177 |
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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(279): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): 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 | a0002c0002t0002g0271 a0002c0002t0002g0272 a0002c0002t0002g0273 |
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 | a0004c0008t0003g0290 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0191 a0001c0001t0001g0192 others(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 | a0002c0003t0002g0016 a0002c0003t0002g0038 a0002c0003t0002g0185 |
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 | a0002c0003t0002g0040 a0002c0003t0002g0041 a0002c0003t0002g0042 others(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 | a0001c0001t0001g0046 a0002c0003t0002g0017 a0002c0003t0002g0018 others(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 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0102 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0007t0001g0068 a0002c0003t0002g0174 a0002c0003t0002g0175 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0172 a0001c0001t0001g0173 others(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 |
24 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
28 | HG01106.hp1 HG01168.hp1 HG01192.hp1 others(25): 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 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(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 | a0002c0002t0002g0228 | 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 | a0001c0004t0001g0293 a0004c0008t0003g0290 |
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 | a0002c0002t0003g0291 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0276 a0001c0004t0001g0278 others(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 | a0001c0004t0001g0282 a0002c0002t0002g0280 a0002c0002t0002g0281 others(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 | a0001c0004t0001g0015 a0001c0004t0001g0035 a0001c0004t0001g0222 others(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 | a0002c0002t0002g0220 | 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 | a0001c0004t0001g0239 a0002c0002t0002g0030 a0002c0002t0002g0217 others(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 | a0002c0002t0002g0279 | 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 | a0001c0004t0001g0226 a0002c0002t0002g0229 a0002c0002t0002g0230 others(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 | a0001c0001t0001g0133 a0002c0003t0003g0010 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0002c0002t0002g0283 a0002c0002t0002g0284 |
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 | a0002c0002t0002g0285 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | 168 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0024 others(165): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): 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 | 44 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(41): Show |
54 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(51): 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 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
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 | a0001c0001t0001g0067 a0001c0004t0001g0293 |
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 | a0004c0008t0003g0290 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0182 a0001c0001t0001g0183 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0004c0008t0003g0290 | 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 | a0001c0001t0001g0046 a0002c0003t0002g0016 a0002c0003t0002g0017 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0004c0008t0003g0290 | 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 | 80 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(77): Show |
93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): 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 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG00558.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.164-6036A>G | CCDC169 | ENSG00000242715.8 | transcript | ENST00000239859.8 | protein_coding | 2/7 | chr13 | 36289738 | |||||||
| chr13:36290232 | G | A | 2 | a0002c0002t0002g0224 a0002c0002t0002g0225 |
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 | a0001c0004t0001g0226 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(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 | a0001c0004t0001g0293 a0004c0008t0003g0290 |
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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0004c0008t0003g0290 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | 169 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(166): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0004c0008t0003g0290 | 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 | a0004c0008t0003g0290 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0207 a0001c0004t0001g0009 a0001c0004t0001g0015 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0002g0220 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0002c0002t0002g0219 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0003g0218 a0002c0002t0003g0291 |
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 | 49 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(46): Show |
59 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(56): 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | 9 | a0001c0001t0001g0023 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
10 | HG01106.hp1 HG01123.hp1 HG01257.hp1 others(7): 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 | a0002c0002t0002g0217 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0005t0001g0058 a0001c0005t0001g0059 a0001c0005t0001g0060 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | 80 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(77): Show |
93 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(90): 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | |||||||
| chr13:36296701 | A | G | 1 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0291 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0002c0002t0003g0218 | 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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0002c0002t0003g0218 | 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 | a0002c0003t0002g0053 a0002c0003t0002g0054 a0002c0003t0002g0055 |
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 | a0002c0002t0002g0292 | 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 | a0002c0002t0002g0217 | 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 | a0002c0002t0002g0217 a0002c0002t0002g0231 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0004t0001g0009 a0001c0004t0001g0015 a0001c0004t0001g0035 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0210 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0046 a0002c0003t0002g0016 a0002c0003t0002g0017 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 |