Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1407 |
| ensemblid | ENSG00000008405.12 |
| hgncid | 2384 |
| symbol | CRY1 |
| name | cryptochrome circadian regulator 1 |
| refseq_nuc | NM_004075.5 |
| refseq_prot | NP_004066.1 |
| ensembl_nuc | ENST00000008527.10 |
| ensembl_prot | ENSP00000008527.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 106991364 |
| end | 107093549 |
| strand | - |
| ver | v1.2 |
| region | chr12:106991364-107093549 |
| region5000 | chr12:106986364-107098549 |
| regionname0 | CRY1_chr12_106991364_107093549 |
| regionname5000 | CRY1_chr12_106986364_107098549 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 586 | 319 | 76 | 61 | 134 | 8 | 38 | 108 | CRY1_chr12_106986364_107098549 | CRY1 | MGVNA others(581): Show |
chr12 | 106986364 | 107098549 |
| a0002 | 0/0 | 586 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | MGVNA others(581): Show |
chr12 | 106986364 | 107098549 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1758 | 256 | 59 | 47 | 118 | 5 | 27 | CRY1_chr12_106986364_107098549 | CRY1 | ATGGG others(1753): Show |
chr12 | 106986364 | 107098549 | ||
| a0001c0002 | 1/1 | 1758 | 57 | 12 | 14 | 15 | 3 | 11 | CRY1_chr12_106986364_107098549 | CRY1 | ATGGG others(1753): Show |
chr12 | 106986364 | 107098549 | ||
| a0001c0003 | 0/0 | 1758 | 4 | 4 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | ATGGG others(1753): Show |
chr12 | 106986364 | 107098549 | ||
| a0001c0004 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | ATGGG others(1753): Show |
chr12 | 106986364 | 107098549 | ||
| a0001c0006 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | ATGGG others(1753): Show |
chr12 | 106986364 | 107098549 | ||
| a0002c0005 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | ATGGG others(1753): Show |
chr12 | 106986364 | 107098549 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2987 | 143 | 11 | 32 | 77 | 5 | 18 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0002 | 0/0 | 2987 | 73 | 19 | 10 | 35 | 0 | 9 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0003 | 0/0 | 2987 | 4 | 4 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0004 | 0/0 | 2987 | 16 | 14 | 2 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0005 | 0/0 | 2987 | 5 | 5 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0007 | 0/0 | 2987 | 3 | 3 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0008 | 0/0 | 2987 | 3 | 2 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0009 | 0/0 | 2987 | 2 | 0 | 2 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0010 | 0/0 | 2987 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0011 | 0/0 | 2987 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0013 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0014 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0001t0015 | 0/0 | 2987 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0002t0003 | 1/1 | 2987 | 56 | 12 | 14 | 15 | 3 | 10 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0002t0012 | 0/0 | 2987 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0003t0006 | 0/0 | 2987 | 4 | 4 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0004t0002 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0001c0006t0001 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| a0002c0005t0002 | 0/0 | 2987 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | AGAGT others(2982): Show |
chr12 | 106986364 | 107098549 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0009g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0009g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0010g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0011g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0011g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0014g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0001t0015g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0011 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0002t0012g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0003t0006g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0003t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0003t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0004t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0001c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| a0002c0005t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0183 | EUR | GBR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0222 | EUR | GBR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0211 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0182 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00673 | hp1 | a0001 | c0001 | t0014 | g0270 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0181 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0074 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0179 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0201 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0202 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0073 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0216 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0198 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0195 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0168 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0178 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01243 | hp2 | a0001 | c0001 | t0015 | g0303 | AMR | PUR | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0217 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0197 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0196 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0209 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0200 | EUR | IBS | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0171 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01928 | hp2 | a0002 | c0005 | t0002 | g0276 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0206 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02027 | hp2 | a0001 | c0001 | t0008 | g0156 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0219 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0189 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02155 | hp1 | a0001 | c0001 | t0011 | g0240 | EAS | CDX | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0282 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0218 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0180 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0203 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0176 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02622 | hp2 | a0001 | c0003 | t0006 | g0162 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0173 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02647 | hp2 | a0001 | c0003 | t0006 | g0161 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0214 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02717 | hp2 | a0001 | c0003 | t0006 | g0008 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0208 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0210 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0227 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0207 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0199 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0226 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0204 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03486 | hp2 | a0001 | c0003 | t0006 | g0008 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0215 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0213 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0175 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0167 | AFR | GWD | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0223 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0205 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03688 | hp2 | a0001 | c0002 | t0012 | g0017 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0011 | SAS | PJL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0220 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0014 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0014 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | STU | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0172 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0030 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | CHB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18941 | hp2 | a0001 | c0001 | t0010 | g0043 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18990 | hp1 | a0001 | c0001 | t0011 | g0239 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0212 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19004 | hp2 | a0001 | c0002 | t0003 | g0221 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | LWK | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19062 | hp2 | a0001 | c0006 | t0001 | g0077 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0174 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19081 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0051 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0191 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | YRI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | ASW | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | ASW | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | GIH | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0228 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | ACB | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | MSL | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | USA | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0194 | AFR | LWK | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | LWK | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0003 | g0177 | REF | REF | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0011 | REF | REF | CRY1_chr12_106986364_107098549 | CRY1 | chr12 | 106986364 | 107098549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106997930 | T | C | 1 | a0002 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1274A>G | p.Asn425Ser | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 8/13 | 1862/2987 | 1274/1761 | 425/586 | chr12 | 106997930 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106997370 | T | C | 1 | a0001c0004 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1509A>G | p.Val503Val | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/13 | 2097/2987 | 1509/1761 | 503/586 | chr12 | 106997370 | |||
| chr12:106997376 | T | A | 1 | a0001c0003 | 4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.1503A>T | p.Ala501Ala | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/13 | 2091/2987 | 1503/1761 | 501/586 | chr12 | 106997376 | |||
| chr12:107001328 | A | G | 5 | a0001c0001 a0001c0003 a0001c0004 others(2): Show |
263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
synonymous_variant | LOW | c.636T>C | p.Gly212Gly | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/13 | 1224/2987 | 636/1761 | 212/586 | chr12 | 107001328 | |||
| chr12:107001852 | T | G | 1 | a0001c0006 | 1 | NA19062.hp2 | synonymous_variant | LOW | c.507A>C | p.Thr169Thr | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/13 | 1095/2987 | 507/1761 | 169/586 | chr12 | 107001852 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106991506 | T | C | 1 | a0001c0001t0011 | 2 | HG02155.hp1 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*496A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1281 | chr12 | 106991506 | ||||||
| chr12:106991586 | C | T | 2 | a0001c0001t0004 a0001c0001t0013 |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*416G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1201 | chr12 | 106991586 | ||||||
| chr12:106991658 | C | T | 1 | a0001c0001t0007 | 3 | HG02818.hp1 HG03139.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*344G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1129 | chr12 | 106991658 | ||||||
| chr12:106991676 | T | G | 1 | a0001c0001t0009 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1111 | chr12 | 106991676 | ||||||
| chr12:106991715 | T | A | 1 | a0001c0001t0010 | 2 | NA18941.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*287A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1072 | chr12 | 106991715 | ||||||
| chr12:106991778 | T | C | 1 | a0001c0001t0014 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 1009 | chr12 | 106991778 | ||||||
| chr12:106991832 | C | A | 7 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(4): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*170G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 13/13 | 955 | chr12 | 106991832 | ||||||
| chr12:107092978 | G | A | 1 | a0001c0001t0013 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 17 | chr12 | 107092978 | ||||||
| chr12:107093085 | G | A | 5 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0014 others(2): Show |
78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-124C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 124 | chr12 | 107093085 | ||||||
| chr12:107093134 | C | T | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(13): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
5_prime_UTR_variant | MODIFIER | c.-173G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 173 | chr12 | 107093134 | ||||||
| chr12:107093269 | G | A | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(3): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
5_prime_UTR_variant | MODIFIER | c.-308C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 308 | chr12 | 107093269 | ||||||
| chr12:107093291 | C | T | 5 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(2): Show |
151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
5_prime_UTR_variant | MODIFIER | c.-330G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 330 | chr12 | 107093291 | ||||||
| chr12:107093296 | A | G | 1 | a0001c0002t0012 | 1 | HG03688.hp2 | 5_prime_UTR_variant | MODIFIER | c.-335T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 335 | chr12 | 107093296 | ||||||
| chr12:107093483 | G | A | 1 | a0001c0001t0015 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-522C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/13 | 522 | chr12 | 107093483 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106992158 | T | C | 1 | a0001c0001t0005g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.*1-157A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992158 | |||||||
| chr12:106992332 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*1-331G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992332 | |||||||
| chr12:106992398 | A | C | 1 | a0001c0001t0002g0244 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1761+389T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992398 | |||||||
| chr12:106992507 | A | G | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1761+280T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992507 | |||||||
| chr12:106992608 | C | G | 1 | a0001c0002t0003g0216 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1761+179G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992608 | |||||||
| chr12:106992617 | A | C | 1 | a0001c0002t0003g0216 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1761+170T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992617 | |||||||
| chr12:106992760 | C | T | 1 | a0001c0002t0003g0196 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1761+27G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 12/12 | chr12 | 106992760 | |||||||
| chr12:106992907 | T | A | 1 | a0001c0001t0002g0280 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1658-17A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 11/12 | chr12 | 106992907 | |||||||
| chr12:106992962 | T | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01167.hp2 HG01169.hp1 |
splice_region_variant&intron_variant | LOW | c.1657+3A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 11/12 | chr12 | 106992962 | |||||||
| chr12:106993247 | A | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
174 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1586-211T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993247 | |||||||
| chr12:106993277 | C | T | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.1586-241G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993277 | |||||||
| chr12:106993308 | G | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0009g0073 others(1): Show |
6 | HG01069.hp1 HG01071.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1586-272C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993308 | |||||||
| chr12:106993385 | C | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1586-349G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993385 | |||||||
| chr12:106993588 | G | A | 7 | a0001c0001t0002g0246 a0001c0001t0002g0259 a0001c0001t0002g0261 others(4): Show |
7 | HG01123.hp1 HG01433.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.1586-552C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993588 | |||||||
| chr12:106993648 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0118 a0001c0001t0001g0120 others(2): Show |
6 | HG01192.hp1 HG01934.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1586-612G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993648 | |||||||
| chr12:106993704 | C | T | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1586-668G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993704 | |||||||
| chr12:106993705 | G | A | 5 | a0001c0001t0002g0237 a0001c0001t0002g0296 a0001c0001t0002g0297 others(2): Show |
5 | HG03195.hp1 HG03579.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1586-669C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993705 | |||||||
| chr12:106993709 | T | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1586-673A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993709 | |||||||
| chr12:106993847 | C | T | 1 | a0001c0002t0003g0187 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1586-811G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106993847 | |||||||
| chr12:106994052 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1586-1016T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994052 | |||||||
| chr12:106994059 | AAAAC | A | 3 | a0001c0001t0005g0225 a0001c0001t0005g0227 a0001c0001t0005g0228 |
3 | HG02109.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1586-1027_1586-102 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994059 | |||||||
| chr12:106994111 | T | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1586-1075A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994111 | |||||||
| chr12:106994119 | A | G | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1586-1083T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994119 | |||||||
| chr12:106994691 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1586-1655G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994691 | |||||||
| chr12:106994732 | A | G | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1586-1696T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994732 | |||||||
| chr12:106994770 | C | A | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.1586-1734G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994770 | |||||||
| chr12:106994830 | A | G | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1586-1794T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994830 | |||||||
| chr12:106994847 | C | T | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1586-1811G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106994847 | |||||||
| chr12:106995168 | AAT | A | 1 | a0001c0001t0001g0001 | 3 | HG01516.hp1 HG06807.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1585+2124_1585+212 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995168 | |||||||
| chr12:106995295 | A | G | 1 | a0001c0001t0004g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1585+1999T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995295 | |||||||
| chr12:106995305 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1585+1989C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995305 | |||||||
| chr12:106995475 | T | C | 1 | a0001c0002t0003g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1585+1819A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995475 | |||||||
| chr12:106995746 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1585+1548G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995746 | |||||||
| chr12:106995818 | C | A | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1585+1476G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995818 | |||||||
| chr12:106995907 | G | A | 1 | a0001c0001t0002g0284 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1585+1387C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106995907 | |||||||
| chr12:106996004 | C | T | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.1585+1290G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996004 | |||||||
| chr12:106996178 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1585+1116A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996178 | |||||||
| chr12:106996204 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1585+1090G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996204 | |||||||
| chr12:106996403 | G | T | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1585+891C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996403 | |||||||
| chr12:106996436 | G | C | 1 | a0001c0001t0001g0023 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1585+858C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996436 | |||||||
| chr12:106996475 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1585+819C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996475 | |||||||
| chr12:106996793 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1585+501T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996793 | |||||||
| chr12:106996906 | T | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1585+388A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996906 | |||||||
| chr12:106996971 | C | A | 1 | a0001c0001t0002g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1585+323G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996971 | |||||||
| chr12:106996972 | A | T | 1 | a0001c0001t0002g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1585+322T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106996972 | |||||||
| chr12:106997089 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1585+205G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106997089 | |||||||
| chr12:106997133 | G | A | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1585+161C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 10/12 | chr12 | 106997133 | |||||||
| chr12:106997890 | T | C | 5 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(2): Show |
6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289+25A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 8/12 | chr12 | 106997890 | |||||||
| chr12:106998154 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1138-88C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998154 | |||||||
| chr12:106998169 | C | A | 1 | a0001c0001t0002g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1138-103G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998169 | |||||||
| chr12:106998346 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1138-280C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998346 | |||||||
| chr12:106998389 | C | T | 1 | a0001c0001t0002g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1138-323G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998389 | |||||||
| chr12:106998399 | A | T | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1138-333T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998399 | |||||||
| chr12:106998543 | G | A | 2 | a0001c0001t0007g0029 a0001c0001t0007g0030 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1138-477C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998543 | |||||||
| chr12:106998587 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1138-521A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998587 | |||||||
| chr12:106998659 | A | AAC | 21 | a0001c0001t0001g0019 a0001c0001t0001g0099 a0001c0001t0001g0106 others(18): Show |
22 | HG00408.hp2 HG00639.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.1138-595_1138-594d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998659 | A | AACAC | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
85 | HG00408.hp1 HG00609.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.1138-597_1138-594d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998659 | A | AACACAC | 22 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0062 others(19): Show |
25 | HG00597.hp1 HG02027.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.1138-599_1138-594d others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998659 | A | AACACACA others(1): Show |
40 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(37): Show |
41 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1138-601_1138-594d others(10): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998659 | A | AACACACA others(3): Show |
11 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0058 others(8): Show |
12 | HG02109.hp1 HG02572.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1138-603_1138-594d others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998659 | A | AACACACA others(5): Show |
10 | a0001c0001t0002g0231 a0001c0001t0002g0233 a0001c0001t0002g0251 others(7): Show |
10 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1138-605_1138-594d others(14): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998659 | A | AACACACA others(7): Show |
30 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0230 others(27): Show |
32 | HG00558.hp1 HG01123.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.1138-607_1138-594d others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998659 | A | AACACACA others(9): Show |
27 | a0001c0001t0002g0229 a0001c0001t0002g0232 a0001c0001t0002g0234 others(24): Show |
27 | HG00558.hp2 HG00673.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1138-609_1138-594d others(18): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998659 | A | AACACACA others(11): Show |
3 | a0001c0001t0002g0235 a0001c0001t0002g0271 a0001c0001t0002g0283 |
3 | HG02145.hp1 HG02735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1138-611_1138-594d others(20): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998659 | A | ACACACAC others(8): Show |
1 | a0001c0001t0002g0245 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1138-594_1138-593i others(17): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998659 | A | ACACACAC others(10): Show |
1 | a0001c0001t0002g0266 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1138-594_1138-593i others(19): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998659 | |||||||
| chr12:106998679 | C | CACACACA others(7): Show |
1 | a0001c0001t0002g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1138-614_1138-613i others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998679 | |||||||
| chr12:106998693 | A | C | 14 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(11): Show |
16 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1138-627T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998693 | |||||||
| chr12:106998790 | C | T | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1138-724G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998790 | |||||||
| chr12:106998857 | A | G | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1137+694T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998857 | |||||||
| chr12:106998867 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1137+684T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998867 | |||||||
| chr12:106998932 | C | G | 3 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137+619G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998932 | |||||||
| chr12:106998939 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA18973.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1137+612C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106998939 | |||||||
| chr12:106999000 | T | C | 99 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(96): Show |
103 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(100): Show |
intron_variant | MODIFIER | c.1137+551A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999000 | |||||||
| chr12:106999043 | C | CA | 23 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0095 others(20): Show |
25 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1137+507dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999043 | |||||||
| chr12:106999073 | G | A | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1137+478C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999073 | |||||||
| chr12:106999266 | T | C | 5 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0250 others(2): Show |
7 | HG00558.hp1 HG03688.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137+285A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999266 | |||||||
| chr12:106999274 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1137+277G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999274 | |||||||
| chr12:106999374 | C | G | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1137+177G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999374 | |||||||
| chr12:106999412 | G | A | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1137+139C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 7/12 | chr12 | 106999412 | |||||||
| chr12:106999894 | A | T | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.826-32T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 6/12 | chr12 | 106999894 | |||||||
| chr12:107000270 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.685-188G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107000270 | |||||||
| chr12:107000300 | TAAATTTC others(4): Show |
T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0069 others(3): Show |
9 | HG01069.hp1 HG01071.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-229_685-219del others(11): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107000300 | |||||||
| chr12:107000322 | C | CAGAA | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-244_685-241dup others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107000322 | |||||||
| chr12:107000356 | T | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.685-274A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107000356 | |||||||
| chr12:107000840 | G | A | 1 | a0001c0002t0003g0180 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.684+440C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107000840 | |||||||
| chr12:107001143 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.684+137C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 5/12 | chr12 | 107001143 | |||||||
| chr12:107001452 | G | A | 1 | a0001c0001t0002g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.596-84C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/12 | chr12 | 107001452 | |||||||
| chr12:107001512 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.596-144A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/12 | chr12 | 107001512 | |||||||
| chr12:107001570 | G | T | 4 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0002g0281 others(1): Show |
4 | HG02602.hp1 NA18943.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+194C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/12 | chr12 | 107001570 | |||||||
| chr12:107001659 | T | C | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.595+105A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/12 | chr12 | 107001659 | |||||||
| chr12:107001735 | G | A | 3 | a0001c0002t0003g0199 a0001c0002t0003g0208 a0001c0002t0003g0210 |
3 | HG02922.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.595+29C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 4/12 | chr12 | 107001735 | |||||||
| chr12:107001960 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.411-12C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107001960 | |||||||
| chr12:107002257 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0116 others(1): Show |
4 | HG00639.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-309C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002257 | |||||||
| chr12:107002355 | G | A | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.411-407C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002355 | |||||||
| chr12:107002575 | T | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
264 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.411-627A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002575 | |||||||
| chr12:107002627 | T | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.411-679A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002627 | |||||||
| chr12:107002957 | G | T | 1 | a0001c0001t0001g0098 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.411-1009C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002957 | |||||||
| chr12:107002998 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.411-1050C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107002998 | |||||||
| chr12:107003019 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.411-1071C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003019 | |||||||
| chr12:107003043 | C | T | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.411-1095G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003043 | |||||||
| chr12:107003354 | T | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.411-1406A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003354 | |||||||
| chr12:107003405 | T | C | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.411-1457A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003405 | |||||||
| chr12:107003450 | C | T | 3 | a0001c0002t0003g0199 a0001c0002t0003g0208 a0001c0002t0003g0210 |
3 | HG02922.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.411-1502G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003450 | |||||||
| chr12:107003736 | T | A | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.410+1370A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003736 | |||||||
| chr12:107003807 | A | AT | 12 | a0001c0001t0001g0099 a0001c0001t0001g0149 a0001c0001t0001g0150 others(9): Show |
13 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.410+1298dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003807 | |||||||
| chr12:107003807 | AT | A | 83 | a0001c0001t0001g0026 a0001c0001t0002g0015 a0001c0001t0002g0016 others(80): Show |
86 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.410+1298delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003807 | |||||||
| chr12:107003810 | T | G | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.410+1296A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003810 | |||||||
| chr12:107003896 | T | A | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.410+1210A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003896 | |||||||
| chr12:107003899 | C | T | 83 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(80): Show |
85 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(82): Show |
intron_variant | MODIFIER | c.410+1207G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003899 | |||||||
| chr12:107003900 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.410+1206C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003900 | |||||||
| chr12:107003919 | C | T | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.410+1187G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107003919 | |||||||
| chr12:107004097 | G | A | 1 | a0001c0001t0002g0286 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.410+1009C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107004097 | |||||||
| chr12:107004103 | C | T | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.410+1003G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107004103 | |||||||
| chr12:107004445 | G | C | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+661C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107004445 | |||||||
| chr12:107004589 | A | G | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.410+517T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107004589 | |||||||
| chr12:107004987 | C | T | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.410+119G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107004987 | |||||||
| chr12:107005003 | T | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.410+103A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 3/12 | chr12 | 107005003 | |||||||
| chr12:107005340 | T | G | 3 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0278 |
3 | NA18940.hp1 NA19079.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.268-92A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005340 | |||||||
| chr12:107005353 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.268-105G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005353 | |||||||
| chr12:107005498 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.268-250A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005498 | |||||||
| chr12:107005525 | C | T | 2 | a0001c0002t0003g0201 a0001c0002t0003g0202 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.268-277G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005525 | |||||||
| chr12:107005655 | C | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
153 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.268-407G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005655 | |||||||
| chr12:107005929 | A | C | 1 | a0001c0002t0003g0213 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.268-681T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107005929 | |||||||
| chr12:107006107 | G | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.268-859C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006107 | |||||||
| chr12:107006362 | C | T | 1 | a0001c0001t0005g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.268-1114G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006362 | |||||||
| chr12:107006372 | T | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0159 |
4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-1124A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006372 | |||||||
| chr12:107006375 | CA | C | 5 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(2): Show |
6 | HG00673.hp1 HG02280.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-1128delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006375 | |||||||
| chr12:107006531 | T | C | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.268-1283A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006531 | |||||||
| chr12:107006536 | T | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0159 |
4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-1288A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006536 | |||||||
| chr12:107006638 | C | CG | 67 | a0001c0001t0002g0016 a0001c0001t0002g0229 a0001c0001t0002g0230 others(64): Show |
68 | HG00558.hp1 HG00558.hp2 HG01123.hp1 others(65): Show |
intron_variant | MODIFIER | c.268-1391_268-1390i others(3): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006638 | |||||||
| chr12:107006638 | C | CGT | 34 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(31): Show |
38 | HG00673.hp1 HG01175.hp1 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.268-1391_268-1390i others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006638 | |||||||
| chr12:107006638 | C | CGTT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
129 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.268-1391_268-1390i others(5): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006638 | |||||||
| chr12:107006638 | C | CGTTT | 16 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0054 others(13): Show |
17 | HG00408.hp1 HG01175.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.268-1391_268-1390i others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006638 | |||||||
| chr12:107006644 | T | G | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.268-1396A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006644 | |||||||
| chr12:107006681 | AGGCTGAA others(7): Show |
A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.268-1447_268-1434d others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006681 | |||||||
| chr12:107006704 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.268-1456A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006704 | |||||||
| chr12:107006739 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.268-1491G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006739 | |||||||
| chr12:107006912 | G | A | 6 | a0001c0001t0004g0160 a0001c0001t0004g0166 a0001c0001t0004g0167 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-1664C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006912 | |||||||
| chr12:107006924 | G | A | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.268-1676C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006924 | |||||||
| chr12:107006976 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.268-1728T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107006976 | |||||||
| chr12:107007122 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.268-1874C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007122 | |||||||
| chr12:107007134 | C | T | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-1886G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007134 | |||||||
| chr12:107007142 | C | T | 2 | a0001c0001t0007g0029 a0001c0001t0007g0030 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.268-1894G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007142 | |||||||
| chr12:107007227 | G | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0109 a0001c0001t0001g0137 |
3 | HG00408.hp2 NA18967.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.268-1979C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007227 | |||||||
| chr12:107007232 | A | G | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.268-1984T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007232 | |||||||
| chr12:107007530 | CT | C | 7 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0124 others(4): Show |
7 | HG01069.hp1 HG01070.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.268-2283delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007530 | |||||||
| chr12:107007533 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.268-2285A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007533 | |||||||
| chr12:107007555 | G | C | 1 | a0002c0005t0002g0276 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.268-2307C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007555 | |||||||
| chr12:107007792 | C | T | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.268-2544G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007792 | |||||||
| chr12:107007830 | C | T | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.268-2582G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007830 | |||||||
| chr12:107007991 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.268-2743A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107007991 | |||||||
| chr12:107008216 | A | G | 2 | a0001c0002t0003g0182 a0001c0002t0003g0183 |
2 | HG00099.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.268-2968T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008216 | |||||||
| chr12:107008274 | A | G | 2 | a0001c0001t0002g0248 a0001c0001t0002g0249 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.268-3026T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008274 | |||||||
| chr12:107008545 | T | C | 1 | a0001c0002t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.268-3297A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008545 | |||||||
| chr12:107008769 | T | C | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.268-3521A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008769 | |||||||
| chr12:107008776 | T | C | 1 | a0001c0001t0002g0279 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.268-3528A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008776 | |||||||
| chr12:107008778 | G | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.268-3530C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008778 | |||||||
| chr12:107008829 | G | A | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268-3581C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008829 | |||||||
| chr12:107008833 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.268-3585C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008833 | |||||||
| chr12:107008911 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.268-3663A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008911 | |||||||
| chr12:107008934 | T | C | 2 | a0001c0001t0002g0248 a0001c0001t0002g0249 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.268-3686A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008934 | |||||||
| chr12:107008935 | C | T | 1 | a0001c0001t0004g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.268-3687G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008935 | |||||||
| chr12:107008946 | T | C | 1 | a0001c0001t0002g0244 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.268-3698A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107008946 | |||||||
| chr12:107009017 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.268-3769C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009017 | |||||||
| chr12:107009313 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.268-4065G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009313 | |||||||
| chr12:107009421 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.268-4173A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009421 | |||||||
| chr12:107009491 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.268-4243C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009491 | |||||||
| chr12:107009525 | C | A | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268-4277G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009525 | |||||||
| chr12:107009558 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.268-4310T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009558 | |||||||
| chr12:107009559 | A | C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0087 others(1): Show |
4 | HG01243.hp1 HG01257.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-4311T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009559 | |||||||
| chr12:107009560 | A | C | 67 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(64): Show |
68 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.268-4312T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009560 | |||||||
| chr12:107009561 | A | C | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.268-4313T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009561 | |||||||
| chr12:107009562 | ACATATAT others(2): Show |
A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0056 others(9): Show |
13 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.268-4323_268-4315d others(11): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009562 | |||||||
| chr12:107009562 | ACATATAT others(4): Show |
A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
42 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.268-4325_268-4315d others(13): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009562 | |||||||
| chr12:107009562 | ACATATAT others(6): Show |
A | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.268-4327_268-4315d others(15): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009562 | |||||||
| chr12:107009563 | C | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(87): Show |
95 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.268-4315G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CAT | 11 | a0001c0002t0003g0014 a0001c0002t0003g0179 a0001c0002t0003g0180 others(8): Show |
11 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.268-4317_268-4316d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CATAT | 8 | a0001c0001t0004g0158 a0001c0001t0005g0226 a0001c0001t0013g0173 others(5): Show |
9 | HG01257.hp2 HG02647.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.268-4319_268-4316d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CATATAT | 12 | a0001c0002t0003g0184 a0001c0002t0003g0188 a0001c0002t0003g0189 others(9): Show |
12 | HG01074.hp1 HG01099.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.268-4321_268-4316d others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CATATATA others(1): Show |
6 | a0001c0002t0003g0010 a0001c0002t0003g0176 a0001c0002t0003g0182 others(3): Show |
6 | HG00642.hp1 HG01255.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-4323_268-4316d others(10): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CATATATA others(3): Show |
6 | a0001c0002t0003g0183 a0001c0002t0003g0185 a0001c0002t0003g0198 others(3): Show |
6 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-4325_268-4316d others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CATATATA others(5): Show |
6 | a0001c0001t0003g0013 a0001c0001t0004g0165 a0001c0002t0003g0174 others(3): Show |
6 | HG02572.hp1 HG03540.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-4327_268-4316d others(14): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CATATATA others(7): Show |
5 | a0001c0001t0003g0013 a0001c0001t0003g0193 a0001c0002t0003g0178 others(2): Show |
5 | HG01192.hp2 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.268-4329_268-4316d others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CATATATA others(9): Show |
2 | a0001c0002t0003g0206 a0001c0003t0006g0008 |
2 | HG02027.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.268-4331_268-4316d others(18): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CATATATA others(11): Show |
7 | a0001c0001t0004g0009 a0001c0001t0004g0164 a0001c0001t0005g0227 others(4): Show |
8 | HG00140.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.268-4333_268-4316d others(20): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CATATATA others(13): Show |
1 | a0001c0002t0012g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.268-4335_268-4316d others(22): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009563 | C | CATATATA others(23): Show |
1 | a0001c0002t0003g0010 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.268-4345_268-4316d others(32): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009563 | |||||||
| chr12:107009565 | T | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(84): Show |
92 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.268-4317A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009565 | |||||||
| chr12:107009565 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0142 a0001c0001t0001g0154 |
3 | HG01123.hp2 HG03486.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.268-4317A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009565 | |||||||
| chr12:107009566 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.268-4329_268-4319d others(13): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009566 | |||||||
| chr12:107009567 | T | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(84): Show |
92 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.268-4319A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009567 | |||||||
| chr12:107009569 | T | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
67 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.268-4321A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009569 | |||||||
| chr12:107009571 | T | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-4323A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009571 | |||||||
| chr12:107009573 | T | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0056 others(11): Show |
15 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.268-4325A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009573 | |||||||
| chr12:107009575 | T | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.268-4327A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009575 | |||||||
| chr12:107009577 | T | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(37): Show |
41 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.268-4329A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009577 | |||||||
| chr12:107009579 | T | A | 23 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(20): Show |
23 | HG00140.hp2 HG01123.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.268-4331A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009579 | |||||||
| chr12:107009581 | T | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0155 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-4333A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009581 | |||||||
| chr12:107009581 | TATATATA others(15): Show |
T | 1 | a0001c0001t0004g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.268-4355_268-4334d others(24): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009581 | |||||||
| chr12:107009583 | T | A | 1 | a0001c0001t0001g0049 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.268-4335A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009583 | |||||||
| chr12:107009583 | TATATATA others(13): Show |
T | 72 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(69): Show |
74 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.268-4355_268-4336d others(22): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009583 | |||||||
| chr12:107009585 | TATATATA others(11): Show |
T | 11 | a0001c0001t0002g0260 a0001c0001t0002g0286 a0001c0001t0002g0287 others(8): Show |
11 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.268-4355_268-4338d others(20): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009585 | |||||||
| chr12:107009587 | TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.268-4355_268-4340d others(18): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009587 | |||||||
| chr12:107009589 | TATATATA others(7): Show |
T | 1 | a0001c0001t0002g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.268-4355_268-4342d others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009589 | |||||||
| chr12:107009591 | TATATATA others(5): Show |
T | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.268-4355_268-4344d others(14): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009591 | |||||||
| chr12:107009593 | TATATATA others(3): Show |
T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(72): Show |
78 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.268-4355_268-4346d others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009593 | |||||||
| chr12:107009595 | TATATATA others(1): Show |
T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0032 others(4): Show |
10 | HG01081.hp1 HG01243.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.268-4355_268-4348d others(10): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009595 | |||||||
| chr12:107009599 | TATAA | T | 5 | a0001c0001t0004g0163 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-4355_268-4352d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009599 | |||||||
| chr12:107009603 | A | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0019 others(63): Show |
69 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.268-4355T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107009603 | |||||||
| chr12:107010028 | G | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0047 |
2 | HG02132.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.268-4780C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010028 | |||||||
| chr12:107010074 | T | A | 1 | a0001c0001t0004g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.268-4826A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010074 | |||||||
| chr12:107010134 | T | TTTTCA | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
264 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.268-4891_268-4887d others(7): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010134 | |||||||
| chr12:107010481 | C | T | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.268-5233G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010481 | |||||||
| chr12:107010514 | G | A | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(73): Show |
78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.268-5266C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010514 | |||||||
| chr12:107010525 | C | G | 1 | a0001c0001t0004g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.268-5277G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010525 | |||||||
| chr12:107010560 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.268-5312G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010560 | |||||||
| chr12:107010561 | A | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268-5313T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010561 | |||||||
| chr12:107010714 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.268-5466G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010714 | |||||||
| chr12:107010788 | GCCATGAA others(6): Show |
G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(88): Show |
97 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.268-5553_268-5541d others(15): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010788 | |||||||
| chr12:107010798 | G | A | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268-5550C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010798 | |||||||
| chr12:107010968 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.268-5720A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107010968 | |||||||
| chr12:107011011 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0001g0124 |
3 | HG00735.hp2 HG01070.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.268-5763T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011011 | |||||||
| chr12:107011012 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.268-5764T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011012 | |||||||
| chr12:107011085 | G | A | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268-5837C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011085 | |||||||
| chr12:107011118 | G | A | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.268-5870C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011118 | |||||||
| chr12:107011121 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.268-5873G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011121 | |||||||
| chr12:107011214 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.268-5966C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011214 | |||||||
| chr12:107011236 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.268-5988C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011236 | |||||||
| chr12:107011354 | A | C | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.268-6106T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011354 | |||||||
| chr12:107011360 | CA | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
256 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.268-6113delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011360 | |||||||
| chr12:107011364 | A | C | 2 | a0001c0001t0005g0228 a0001c0002t0003g0206 |
2 | HG02027.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.268-6116T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011364 | |||||||
| chr12:107011365 | A | C | 8 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0150 others(5): Show |
8 | HG00099.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.268-6117T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011365 | |||||||
| chr12:107011489 | G | A | 2 | a0001c0002t0003g0184 a0001c0002t0003g0185 |
2 | NA18989.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.268-6241C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011489 | |||||||
| chr12:107011668 | T | G | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268-6420A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011668 | |||||||
| chr12:107011678 | G | C | 1 | a0001c0001t0005g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.268-6430C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011678 | |||||||
| chr12:107011711 | G | A | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.268-6463C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011711 | |||||||
| chr12:107011813 | A | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(33): Show |
38 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.268-6565T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011813 | |||||||
| chr12:107011840 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.268-6592C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011840 | |||||||
| chr12:107011898 | A | C | 2 | a0001c0001t0005g0225 a0001c0001t0005g0227 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.268-6650T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107011898 | |||||||
| chr12:107012049 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.268-6801C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012049 | |||||||
| chr12:107012144 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.268-6896G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012144 | |||||||
| chr12:107012163 | G | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.268-6915C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012163 | |||||||
| chr12:107012203 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.268-6955C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012203 | |||||||
| chr12:107012244 | G | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0159 |
4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-6996C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012244 | |||||||
| chr12:107012353 | T | C | 5 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(2): Show |
6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-7105A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012353 | |||||||
| chr12:107012354 | C | G | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268-7106G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012354 | |||||||
| chr12:107012363 | C | A | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.268-7115G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012363 | |||||||
| chr12:107012374 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.268-7126G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012374 | |||||||
| chr12:107012375 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.268-7127T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012375 | |||||||
| chr12:107012630 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.268-7382T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012630 | |||||||
| chr12:107012710 | A | C | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.268-7462T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107012710 | |||||||
| chr12:107013038 | C | T | 1 | a0001c0002t0003g0200 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.268-7790G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013038 | |||||||
| chr12:107013054 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.268-7806C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013054 | |||||||
| chr12:107013188 | A | C | 1 | a0001c0001t0001g0039 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.268-7940T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013188 | |||||||
| chr12:107013239 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-7991G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013239 | |||||||
| chr12:107013289 | T | A | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.268-8041A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013289 | |||||||
| chr12:107013323 | A | G | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.268-8075T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013323 | |||||||
| chr12:107013505 | T | C | 2 | a0001c0001t0007g0029 a0001c0001t0007g0030 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.268-8257A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013505 | |||||||
| chr12:107013724 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267+8360G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013724 | |||||||
| chr12:107013760 | C | T | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.267+8324G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013760 | |||||||
| chr12:107013796 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.267+8288C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013796 | |||||||
| chr12:107013818 | A | G | 1 | a0001c0002t0003g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.267+8266T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013818 | |||||||
| chr12:107013996 | T | C | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+8088A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107013996 | |||||||
| chr12:107014027 | C | T | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.267+8057G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014027 | |||||||
| chr12:107014133 | AC | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0024 others(47): Show |
51 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.267+7950delG | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014133 | |||||||
| chr12:107014240 | T | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
264 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.267+7844A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014240 | |||||||
| chr12:107014299 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.267+7785A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014299 | |||||||
| chr12:107014359 | G | A | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+7725C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014359 | |||||||
| chr12:107014379 | G | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.267+7705C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014379 | |||||||
| chr12:107014380 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.267+7704C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014380 | |||||||
| chr12:107014404 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.267+7680T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014404 | |||||||
| chr12:107014470 | T | C | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.267+7614A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014470 | |||||||
| chr12:107014588 | TACTA | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
157 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.267+7492_267+7495d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014588 | |||||||
| chr12:107014626 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.267+7458T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014626 | |||||||
| chr12:107014689 | G | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.267+7395C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014689 | |||||||
| chr12:107014775 | C | A | 3 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0002g0302 |
3 | HG02602.hp1 NA18943.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.267+7309G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014775 | |||||||
| chr12:107014919 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.267+7165C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107014919 | |||||||
| chr12:107015167 | C | T | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.267+6917G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015167 | |||||||
| chr12:107015206 | C | T | 3 | a0001c0001t0002g0236 a0001c0001t0002g0283 a0001c0004t0002g0282 |
3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.267+6878G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015206 | |||||||
| chr12:107015344 | CT | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
171 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.267+6739delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015344 | |||||||
| chr12:107015359 | A | G | 3 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+6725T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015359 | |||||||
| chr12:107015369 | T | A | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.267+6715A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015369 | |||||||
| chr12:107015370 | C | A | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.267+6714G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015370 | |||||||
| chr12:107015492 | C | T | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.267+6592G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015492 | |||||||
| chr12:107015506 | G | A | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.267+6578C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015506 | |||||||
| chr12:107015536 | G | A | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.267+6548C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015536 | |||||||
| chr12:107015598 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | HG00609.hp1 NA18943.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+6486C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015598 | |||||||
| chr12:107015706 | G | A | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.267+6378C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015706 | |||||||
| chr12:107015764 | G | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+6320C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015764 | |||||||
| chr12:107015898 | C | A | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.267+6186G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107015898 | |||||||
| chr12:107016018 | T | C | 2 | a0001c0003t0006g0161 a0001c0003t0006g0162 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.267+6066A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016018 | |||||||
| chr12:107016045 | C | G | 3 | a0001c0001t0002g0236 a0001c0001t0002g0283 a0001c0004t0002g0282 |
3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.267+6039G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016045 | |||||||
| chr12:107016110 | G | T | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.267+5974C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016110 | |||||||
| chr12:107016116 | G | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.267+5968C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016116 | |||||||
| chr12:107016126 | A | G | 1 | a0001c0002t0003g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.267+5958T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016126 | |||||||
| chr12:107016161 | T | C | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.267+5923A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016161 | |||||||
| chr12:107016274 | C | T | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.267+5810G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016274 | |||||||
| chr12:107016324 | A | G | 1 | a0001c0001t0004g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.267+5760T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016324 | |||||||
| chr12:107016370 | A | T | 1 | a0001c0001t0002g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.267+5714T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016370 | |||||||
| chr12:107016841 | C | T | 1 | a0001c0001t0005g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.267+5243G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107016841 | |||||||
| chr12:107017053 | C | T | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.267+5031G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017053 | |||||||
| chr12:107017082 | G | A | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.267+5002C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017082 | |||||||
| chr12:107017156 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.267+4928G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017156 | |||||||
| chr12:107017157 | G | A | 1 | a0001c0002t0003g0187 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.267+4927C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017157 | |||||||
| chr12:107017537 | T | C | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.267+4547A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017537 | |||||||
| chr12:107017645 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0015g0303 |
2 | HG01243.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.267+4439G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017645 | |||||||
| chr12:107017686 | A | G | 1 | a0001c0001t0002g0281 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.267+4398T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017686 | |||||||
| chr12:107017799 | C | A | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.267+4285G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017799 | |||||||
| chr12:107017827 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.267+4257G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107017827 | |||||||
| chr12:107018013 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.267+4071G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018013 | |||||||
| chr12:107018276 | T | C | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.267+3808A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018276 | |||||||
| chr12:107018424 | T | C | 3 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+3660A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018424 | |||||||
| chr12:107018484 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.267+3600C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018484 | |||||||
| chr12:107018528 | A | G | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.267+3556T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018528 | |||||||
| chr12:107018600 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.267+3484T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018600 | |||||||
| chr12:107018672 | C | T | 13 | a0001c0001t0002g0246 a0001c0001t0002g0259 a0001c0001t0002g0260 others(10): Show |
13 | HG01123.hp1 HG01433.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.267+3412G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018672 | |||||||
| chr12:107018731 | A | C | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.267+3353T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018731 | |||||||
| chr12:107018752 | A | G | 4 | a0001c0002t0003g0175 a0001c0002t0003g0176 a0001c0002t0003g0209 others(1): Show |
4 | HG01361.hp2 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+3332T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018752 | |||||||
| chr12:107018859 | G | C | 7 | a0001c0001t0002g0232 a0001c0001t0002g0286 a0001c0001t0002g0287 others(4): Show |
7 | HG01943.hp1 NA18948.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.267+3225C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107018859 | |||||||
| chr12:107019074 | C | G | 1 | a0001c0001t0002g0264 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.267+3010G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019074 | |||||||
| chr12:107019092 | AG | A | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.267+2991delC | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019092 | |||||||
| chr12:107019123 | G | T | 1 | a0001c0002t0003g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.267+2961C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019123 | |||||||
| chr12:107019216 | CT | C | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.267+2867delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019216 | |||||||
| chr12:107019510 | A | G | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.267+2574T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019510 | |||||||
| chr12:107019644 | A | ACTAGGG | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+2434_267+2439d others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019644 | |||||||
| chr12:107019863 | G | A | 1 | a0001c0001t0004g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.267+2221C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019863 | |||||||
| chr12:107019910 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.267+2174G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107019910 | |||||||
| chr12:107020186 | C | CA | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
246 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.267+1897dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020186 | |||||||
| chr12:107020186 | C | CAA | 15 | a0001c0001t0001g0120 a0001c0001t0002g0232 a0001c0001t0002g0242 others(12): Show |
15 | HG01943.hp1 HG02300.hp1 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.267+1896_267+1897d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020186 | |||||||
| chr12:107020229 | G | C | 2 | a0001c0002t0003g0189 a0001c0002t0003g0220 |
2 | HG02145.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.267+1855C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020229 | |||||||
| chr12:107020316 | T | C | 1 | a0001c0002t0003g0180 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.267+1768A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020316 | |||||||
| chr12:107020381 | T | C | 1 | a0001c0002t0003g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.267+1703A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020381 | |||||||
| chr12:107020395 | T | C | 1 | a0001c0002t0003g0186 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.267+1689A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020395 | |||||||
| chr12:107020471 | T | C | 1 | a0001c0001t0002g0265 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.267+1613A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020471 | |||||||
| chr12:107020525 | G | GT | 80 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(77): Show |
82 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.267+1558dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020525 | |||||||
| chr12:107020525 | GT | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
180 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.267+1558delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020525 | |||||||
| chr12:107020565 | C | T | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.267+1519G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020565 | |||||||
| chr12:107020681 | C | T | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+1403G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020681 | |||||||
| chr12:107020687 | G | T | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.267+1397C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107020687 | |||||||
| chr12:107021096 | C | G | 1 | a0001c0001t0003g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.267+988G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021096 | |||||||
| chr12:107021152 | G | A | 2 | a0001c0003t0006g0161 a0001c0003t0006g0162 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.267+932C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021152 | |||||||
| chr12:107021156 | G | A | 3 | a0001c0001t0002g0236 a0001c0001t0002g0283 a0001c0004t0002g0282 |
3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.267+928C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021156 | |||||||
| chr12:107021228 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.267+856G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021228 | |||||||
| chr12:107021261 | C | T | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(73): Show |
78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.267+823G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021261 | |||||||
| chr12:107021295 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.267+789T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021295 | |||||||
| chr12:107021350 | T | C | 5 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02630.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+734A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021350 | |||||||
| chr12:107021352 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.267+732C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021352 | |||||||
| chr12:107021379 | C | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.267+705G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021379 | |||||||
| chr12:107021386 | T | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.267+698A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021386 | |||||||
| chr12:107021460 | C | G | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.267+624G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021460 | |||||||
| chr12:107021525 | T | C | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+559A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021525 | |||||||
| chr12:107021657 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
264 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.267+427G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021657 | |||||||
| chr12:107021663 | C | T | 5 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(2): Show |
6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+421G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021663 | |||||||
| chr12:107021701 | CAT | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0047 a0001c0001t0001g0052 others(3): Show |
6 | HG00609.hp1 HG02132.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+381_267+382del others(2): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021701 | |||||||
| chr12:107021725 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.267+359G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021725 | |||||||
| chr12:107021729 | A | T | 1 | a0001c0002t0003g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.267+355T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021729 | |||||||
| chr12:107021741 | T | C | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(73): Show |
78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.267+343A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021741 | |||||||
| chr12:107021749 | C | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.267+335G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021749 | |||||||
| chr12:107021772 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.267+312C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021772 | |||||||
| chr12:107021815 | T | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.267+269A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021815 | |||||||
| chr12:107021878 | T | C | 3 | a0001c0001t0002g0233 a0001c0001t0002g0263 a0001c0001t0002g0300 |
3 | HG02257.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.267+206A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 2/12 | chr12 | 107021878 | |||||||
| chr12:107022373 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.159-181T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022373 | |||||||
| chr12:107022470 | A | C | 2 | a0001c0001t0004g0007 a0001c0001t0004g0157 |
3 | HG02280.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.159-278T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022470 | |||||||
| chr12:107022493 | T | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-301A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022493 | |||||||
| chr12:107022553 | A | G | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.159-361T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022553 | |||||||
| chr12:107022770 | AAAAG | A | 5 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(2): Show |
6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-582_159-579del others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022770 | |||||||
| chr12:107022813 | T | C | 3 | a0001c0001t0002g0236 a0001c0001t0002g0283 a0001c0004t0002g0282 |
3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.159-621A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022813 | |||||||
| chr12:107022845 | TA | T | 81 | a0001c0001t0001g0018 a0001c0001t0001g0139 a0001c0001t0002g0015 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-654delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022845 | |||||||
| chr12:107022999 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.159-807C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107022999 | |||||||
| chr12:107023063 | ATTAT | A | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-875_159-872del others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023063 | |||||||
| chr12:107023149 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-957A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023149 | |||||||
| chr12:107023270 | G | A | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-1078C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023270 | |||||||
| chr12:107023287 | G | T | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-1095C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023287 | |||||||
| chr12:107023404 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.159-1212C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023404 | |||||||
| chr12:107023588 | G | A | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-1396C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023588 | |||||||
| chr12:107023866 | G | C | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-1674C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023866 | |||||||
| chr12:107023945 | T | A | 1 | a0001c0001t0002g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159-1753A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107023945 | |||||||
| chr12:107024013 | C | G | 1 | a0001c0001t0002g0265 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.159-1821G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024013 | |||||||
| chr12:107024300 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.159-2108G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024300 | |||||||
| chr12:107024699 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.159-2507G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024699 | |||||||
| chr12:107024721 | T | A | 3 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0159 |
4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-2529A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024721 | |||||||
| chr12:107024848 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-2656G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024848 | |||||||
| chr12:107024885 | T | TA | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-2694dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107024885 | |||||||
| chr12:107025036 | T | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-2844A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025036 | |||||||
| chr12:107025193 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.159-3001G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025193 | |||||||
| chr12:107025266 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0011g0239 |
3 | HG00140.hp2 HG01261.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.159-3074G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025266 | |||||||
| chr12:107025274 | A | T | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-3082T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025274 | |||||||
| chr12:107025282 | T | C | 1 | a0001c0001t0003g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.159-3090A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025282 | |||||||
| chr12:107025479 | G | A | 1 | a0001c0001t0005g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159-3287C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025479 | |||||||
| chr12:107025807 | T | G | 1 | a0001c0002t0003g0012 | 2 | NA18975.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.159-3615A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025807 | |||||||
| chr12:107025884 | C | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-3692G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107025884 | |||||||
| chr12:107026111 | AAT | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
6 | HG00735.hp2 HG01070.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-3921_159-3920d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026111 | |||||||
| chr12:107026134 | C | CATATAAT others(34): Show |
1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159-3943_159-3942i others(43): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | |||||||
| chr12:107026134 | C | CATATATA others(204): Show |
1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-3943_159-3942i others(213): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | |||||||
| chr12:107026134 | C | CATATATA others(88): Show |
4 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0168 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-3943_159-3942i others(97): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | |||||||
| chr12:107026134 | C | CATATATA others(118): Show |
4 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0170 others(1): Show |
5 | HG01884.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-3943_159-3942i others(127): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | |||||||
| chr12:107026134 | C | CATATATA others(146): Show |
2 | a0001c0001t0004g0164 a0001c0001t0004g0165 |
2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.159-3943_159-3942i others(155): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | |||||||
| chr12:107026134 | C | CATATATA others(25): Show |
1 | a0001c0002t0003g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159-3974_159-3943d others(34): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | |||||||
| chr12:107026134 | C | CATATATG others(155): Show |
2 | a0001c0001t0004g0007 a0001c0001t0004g0157 |
3 | HG02280.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.159-3943_159-3942i others(164): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | |||||||
| chr12:107026134 | C | CATATATG others(155): Show |
1 | a0001c0001t0004g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.159-3943_159-3942i others(164): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026134 | |||||||
| chr12:107026143 | T | TACATATA others(152): Show |
1 | a0001c0001t0004g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.159-3952_159-3951i others(161): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026143 | |||||||
| chr12:107026147 | T | TAAATAAC others(60): Show |
1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(69): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(64): Show |
7 | a0001c0001t0001g0052 a0001c0001t0001g0099 a0001c0001t0001g0102 others(4): Show |
7 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(73): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(145): Show |
1 | a0001c0001t0002g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159-3956_159-3955i others(154): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(62): Show |
102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
106 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(71): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(92): Show |
22 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0033 others(19): Show |
23 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(101): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(122): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0148 |
2 | HG01261.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.159-3956_159-3955i others(131): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(60): Show |
12 | a0001c0001t0001g0042 a0001c0001t0001g0149 a0001c0001t0001g0150 others(9): Show |
12 | HG02109.hp1 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(69): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(88): Show |
2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-3956_159-3955i others(97): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(328): Show |
1 | a0001c0001t0002g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(337): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(120): Show |
36 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(33): Show |
38 | HG00558.hp2 HG01175.hp1 HG01943.hp1 others(35): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(129): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(150): Show |
17 | a0001c0001t0002g0233 a0001c0001t0002g0235 a0001c0001t0002g0236 others(14): Show |
17 | HG00673.hp1 HG01978.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(159): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(180): Show |
11 | a0001c0001t0002g0246 a0001c0001t0002g0259 a0001c0001t0002g0261 others(8): Show |
11 | HG00558.hp1 HG01123.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.159-3956_159-3955i others(189): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(300): Show |
1 | a0001c0001t0002g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(309): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(330): Show |
1 | a0001c0001t0002g0268 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(339): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(150): Show |
1 | a0001c0001t0002g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.159-3956_159-3955i others(159): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(178): Show |
1 | a0001c0001t0002g0263 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.159-3956_159-3955i others(187): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(206): Show |
1 | a0001c0001t0002g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.159-3956_159-3955i others(215): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(146): Show |
1 | a0001c0001t0002g0238 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(155): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(147): Show |
2 | a0001c0001t0002g0248 a0001c0001t0002g0249 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.159-3956_159-3955i others(156): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026147 | T | TATATAAC others(148): Show |
1 | a0001c0001t0002g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.159-3956_159-3955i others(157): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026147 | |||||||
| chr12:107026149 | T | TATAAC | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-3958_159-3957i others(7): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026149 | |||||||
| chr12:107026149 | T | TATAACAT others(118): Show |
1 | a0001c0001t0002g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.159-3958_159-3957i others(127): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026149 | |||||||
| chr12:107026149 | T | TATAACAT others(49): Show |
3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-3958_159-3957i others(58): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026149 | |||||||
| chr12:107026152 | A | AACATATA others(64): Show |
1 | a0001c0001t0001g0001 | 3 | HG01516.hp1 HG06807.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.159-3961_159-3960i others(73): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026152 | |||||||
| chr12:107026157 | A | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
234 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.159-3965T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026157 | |||||||
| chr12:107026158 | A | C | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-3966T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026158 | |||||||
| chr12:107026158 | AAT | A | 2 | a0001c0001t0001g0001 a0001c0001t0015g0303 |
4 | HG01243.hp2 HG01516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-3968_159-3967d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026158 | |||||||
| chr12:107026160 | T | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
234 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.159-3968A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026160 | |||||||
| chr12:107026160 | T | TATATATA others(21): Show |
1 | a0001c0002t0003g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.159-3969_159-3968i others(30): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026160 | |||||||
| chr12:107026162 | T | TATATGTT others(53): Show |
3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-3971_159-3970i others(62): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026162 | |||||||
| chr12:107026164 | T | A | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-3972A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026164 | |||||||
| chr12:107026183 | T | C | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159-3991A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026183 | |||||||
| chr12:107026295 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0129 |
2 | NA19011.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.159-4103C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026295 | |||||||
| chr12:107026404 | T | C | 1 | a0001c0001t0008g0172 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.159-4212A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026404 | |||||||
| chr12:107026430 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.159-4238G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026430 | |||||||
| chr12:107026643 | T | C | 1 | a0001c0001t0002g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.159-4451A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026643 | |||||||
| chr12:107026667 | T | C | 3 | a0001c0002t0003g0190 a0001c0002t0003g0206 a0001c0002t0003g0212 |
3 | HG02027.hp1 NA18963.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.159-4475A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026667 | |||||||
| chr12:107026769 | G | GT | 13 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 others(10): Show |
15 | HG00140.hp1 HG01074.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.159-4578dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026769 | |||||||
| chr12:107026769 | GT | G | 62 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(59): Show |
64 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.159-4578delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026769 | |||||||
| chr12:107026769 | GTT | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0061 others(21): Show |
27 | HG01516.hp1 HG01943.hp1 HG02027.hp2 others(24): Show |
intron_variant | MODIFIER | c.159-4579_159-4578d others(4): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026769 | |||||||
| chr12:107026769 | GTTT | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
149 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.159-4580_159-4578d others(5): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026769 | |||||||
| chr12:107026769 | GTTTT | G | 12 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(9): Show |
12 | HG01167.hp1 HG01167.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.159-4581_159-4578d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107026769 | |||||||
| chr12:107027477 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01175.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.159-5285T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107027477 | |||||||
| chr12:107027483 | T | A | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-5291A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107027483 | |||||||
| chr12:107028500 | C | T | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-6308G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107028500 | |||||||
| chr12:107028552 | A | T | 1 | a0001c0001t0002g0254 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.159-6360T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107028552 | |||||||
| chr12:107028803 | T | C | 1 | a0001c0002t0003g0219 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.159-6611A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107028803 | |||||||
| chr12:107029179 | G | GTGCA | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-6991_159-6988d others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029179 | |||||||
| chr12:107029402 | A | G | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-7210T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029402 | |||||||
| chr12:107029428 | C | T | 3 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0159 |
4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-7236G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029428 | |||||||
| chr12:107029451 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-7259C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029451 | |||||||
| chr12:107029497 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.159-7305C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029497 | |||||||
| chr12:107029538 | C | A | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-7346G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029538 | |||||||
| chr12:107029606 | C | CA | 77 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(74): Show |
79 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.159-7415dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029606 | |||||||
| chr12:107029606 | CA | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.159-7415delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029606 | |||||||
| chr12:107029637 | T | A | 3 | a0001c0002t0003g0198 a0001c0002t0003g0201 a0001c0002t0003g0202 |
3 | HG01070.hp2 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.159-7445A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029637 | |||||||
| chr12:107029677 | T | G | 1 | a0001c0001t0002g0302 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.159-7485A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029677 | |||||||
| chr12:107029799 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.159-7607T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107029799 | |||||||
| chr12:107030205 | A | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-8013T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107030205 | |||||||
| chr12:107030331 | C | A | 1 | a0001c0002t0003g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.159-8139G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107030331 | |||||||
| chr12:107030952 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.159-8760C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107030952 | |||||||
| chr12:107031029 | A | C | 3 | a0001c0001t0002g0268 a0001c0001t0002g0269 a0001c0001t0002g0277 |
3 | HG02109.hp2 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.159-8837T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031029 | |||||||
| chr12:107031115 | A | AAAC | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-8926_159-8924d others(5): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031115 | |||||||
| chr12:107031223 | T | C | 1 | a0001c0001t0002g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.159-9031A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031223 | |||||||
| chr12:107031338 | C | A | 1 | a0001c0002t0003g0212 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.159-9146G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031338 | |||||||
| chr12:107031370 | C | CT | 9 | a0001c0001t0001g0041 a0001c0001t0001g0122 a0001c0001t0001g0128 others(6): Show |
9 | HG01074.hp2 HG01256.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.159-9179dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031370 | |||||||
| chr12:107031416 | T | C | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159-9224A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031416 | |||||||
| chr12:107031801 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159-9609A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031801 | |||||||
| chr12:107031860 | T | C | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.159-9668A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031860 | |||||||
| chr12:107031948 | T | G | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-9756A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031948 | |||||||
| chr12:107031991 | G | C | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-9799C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107031991 | |||||||
| chr12:107032046 | T | C | 1 | a0001c0002t0003g0215 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.159-9854A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032046 | |||||||
| chr12:107032123 | G | A | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-9931C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032123 | |||||||
| chr12:107032373 | A | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-10181T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032373 | |||||||
| chr12:107032394 | G | A | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.159-10202C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032394 | |||||||
| chr12:107032490 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.159-10298G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032490 | |||||||
| chr12:107032505 | T | TACAA | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | NA18612.hp1 NA18947.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.159-10314_159-1031 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032505 | |||||||
| chr12:107032507 | C | CAA | 46 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(43): Show |
47 | HG00597.hp1 HG00673.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.159-10316_159-1031 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032507 | |||||||
| chr12:107032509 | G | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(48): Show |
52 | HG00597.hp1 HG00673.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.159-10317C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032509 | |||||||
| chr12:107032509 | G | GAC | 55 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(52): Show |
57 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.159-10319_159-1031 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032509 | |||||||
| chr12:107032509 | G | GACAC | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(35): Show |
42 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.159-10321_159-1031 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032509 | |||||||
| chr12:107032509 | G | GACACAC | 7 | a0001c0001t0001g0006 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
8 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.159-10323_159-1031 others(10): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032509 | |||||||
| chr12:107032584 | C | T | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-10392G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032584 | |||||||
| chr12:107032826 | T | A | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-10634A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107032826 | |||||||
| chr12:107033003 | C | T | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-10811G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033003 | |||||||
| chr12:107033264 | T | G | 3 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0159 |
4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-11072A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033264 | |||||||
| chr12:107033353 | A | C | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG02257.hp2 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-11161T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033353 | |||||||
| chr12:107033376 | G | A | 8 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0271 others(5): Show |
8 | HG02559.hp2 HG02735.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.159-11184C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033376 | |||||||
| chr12:107033724 | T | C | 2 | a0001c0001t0007g0029 a0001c0001t0007g0030 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.159-11532A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033724 | |||||||
| chr12:107033770 | G | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.159-11578C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033770 | |||||||
| chr12:107033932 | G | C | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-11740C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107033932 | |||||||
| chr12:107034136 | G | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
260 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.159-11944C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034136 | |||||||
| chr12:107034261 | C | T | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-12069G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034261 | |||||||
| chr12:107034312 | G | C | 1 | a0001c0001t0002g0288 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.159-12120C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034312 | |||||||
| chr12:107034349 | G | A | 1 | a0001c0002t0003g0221 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.159-12157C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034349 | |||||||
| chr12:107034508 | C | T | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-12316G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034508 | |||||||
| chr12:107034609 | C | A | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-12417G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034609 | |||||||
| chr12:107034633 | T | C | 5 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02630.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-12441A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034633 | |||||||
| chr12:107034781 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.159-12589T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107034781 | |||||||
| chr12:107035138 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.159-12946T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107035138 | |||||||
| chr12:107035263 | T | G | 1 | a0001c0001t0002g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.159-13071A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107035263 | |||||||
| chr12:107035345 | C | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0070 |
3 | HG02683.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.159-13153G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107035345 | |||||||
| chr12:107035376 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.159-13184A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107035376 | |||||||
| chr12:107035823 | T | C | 8 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(5): Show |
9 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.159-13631A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107035823 | |||||||
| chr12:107036004 | A | G | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-13812T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036004 | |||||||
| chr12:107036102 | T | C | 1 | a0001c0001t0002g0244 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.159-13910A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036102 | |||||||
| chr12:107036128 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0129 |
2 | NA19011.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.159-13936C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036128 | |||||||
| chr12:107036137 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.159-13945A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036137 | |||||||
| chr12:107036274 | T | C | 1 | a0001c0001t0005g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159-14082A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036274 | |||||||
| chr12:107036583 | TGG | T | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-14393_159-1439 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036583 | |||||||
| chr12:107036585 | G | GT | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0041 others(7): Show |
11 | HG01261.hp2 HG03209.hp2 HG04184.hp2 others(8): Show |
intron_variant | MODIFIER | c.159-14394dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036585 | |||||||
| chr12:107036585 | GT | G | 70 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(67): Show |
72 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.159-14394delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036585 | |||||||
| chr12:107036736 | A | G | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-14544T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036736 | |||||||
| chr12:107036761 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.159-14569T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036761 | |||||||
| chr12:107036913 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-14721G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036913 | |||||||
| chr12:107036972 | T | C | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(73): Show |
78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.159-14780A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107036972 | |||||||
| chr12:107037178 | G | A | 2 | a0001c0002t0003g0201 a0001c0002t0003g0202 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.159-14986C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037178 | |||||||
| chr12:107037446 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.159-15254G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037446 | |||||||
| chr12:107037658 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-15466C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037658 | |||||||
| chr12:107037697 | TTTTA | T | 86 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(83): Show |
89 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.159-15509_159-1550 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037697 | |||||||
| chr12:107037766 | T | A | 1 | a0001c0002t0003g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.159-15574A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037766 | |||||||
| chr12:107037911 | G | A | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-15719C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107037911 | |||||||
| chr12:107038034 | T | C | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.159-15842A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038034 | |||||||
| chr12:107038255 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.159-16063A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038255 | |||||||
| chr12:107038284 | C | T | 1 | a0001c0001t0005g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159-16092G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038284 | |||||||
| chr12:107038378 | G | A | 2 | a0001c0001t0002g0241 a0001c0001t0002g0267 |
2 | HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.159-16186C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038378 | |||||||
| chr12:107038403 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.159-16211T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038403 | |||||||
| chr12:107038712 | C | T | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG02257.hp2 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-16520G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107038712 | |||||||
| chr12:107039076 | G | A | 1 | a0001c0002t0003g0014 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.159-16884C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039076 | |||||||
| chr12:107039080 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.159-16888C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039080 | |||||||
| chr12:107039159 | T | C | 1 | a0001c0001t0007g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.159-16967A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039159 | |||||||
| chr12:107039380 | A | C | 3 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 |
3 | HG02818.hp1 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.159-17188T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039380 | |||||||
| chr12:107039559 | T | C | 1 | a0001c0001t0002g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.159-17367A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039559 | |||||||
| chr12:107039606 | A | T | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-17414T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039606 | |||||||
| chr12:107039644 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.159-17452C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039644 | |||||||
| chr12:107039796 | C | T | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-17604G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039796 | |||||||
| chr12:107039894 | C | T | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.159-17702G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107039894 | |||||||
| chr12:107040089 | G | C | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-17897C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040089 | |||||||
| chr12:107040254 | G | C | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-18062C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040254 | |||||||
| chr12:107040271 | CT | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.159-18080delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040271 | |||||||
| chr12:107040285 | T | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0067 others(4): Show |
7 | HG01081.hp1 HG02135.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-18093A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040285 | |||||||
| chr12:107040286 | A | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0067 others(4): Show |
7 | HG01081.hp1 HG02135.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-18094T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040286 | |||||||
| chr12:107040287 | G | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0067 others(4): Show |
7 | HG01081.hp1 HG02135.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-18095C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040287 | |||||||
| chr12:107040287 | GT | G | 86 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(83): Show |
89 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.159-18096delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040287 | |||||||
| chr12:107040287 | GTT | G | 14 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(11): Show |
16 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.159-18097_159-1809 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040287 | |||||||
| chr12:107040309 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-18117C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040309 | |||||||
| chr12:107040316 | C | T | 2 | a0001c0001t0005g0225 a0001c0001t0005g0227 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.159-18124G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040316 | |||||||
| chr12:107040336 | AG | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.159-18145delC | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040336 | |||||||
| chr12:107040393 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-18201A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040393 | |||||||
| chr12:107040411 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-18219C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040411 | |||||||
| chr12:107040646 | T | C | 1 | a0001c0001t0002g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.159-18454A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040646 | |||||||
| chr12:107040783 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.159-18591A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040783 | |||||||
| chr12:107040873 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.159-18681C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040873 | |||||||
| chr12:107040919 | T | TA | 9 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
10 | HG01167.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.159-18728dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040919 | |||||||
| chr12:107040926 | A | G | 2 | a0001c0001t0002g0248 a0001c0001t0002g0249 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.159-18734T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040926 | |||||||
| chr12:107040941 | G | GA | 5 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(2): Show |
6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-18750dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040941 | |||||||
| chr12:107040990 | T | A | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-18798A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107040990 | |||||||
| chr12:107041093 | C | A | 1 | a0001c0002t0003g0195 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.159-18901G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041093 | |||||||
| chr12:107041121 | G | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG01167.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.159-18929C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041121 | |||||||
| chr12:107041191 | C | T | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-18999G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041191 | |||||||
| chr12:107041240 | C | T | 1 | a0001c0002t0003g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159-19048G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041240 | |||||||
| chr12:107041594 | A | G | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-19402T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041594 | |||||||
| chr12:107041621 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159-19429A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041621 | |||||||
| chr12:107041627 | A | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
260 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.159-19435T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041627 | |||||||
| chr12:107041772 | A | G | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-19580T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041772 | |||||||
| chr12:107041773 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.159-19581A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041773 | |||||||
| chr12:107041923 | G | A | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-19731C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041923 | |||||||
| chr12:107041930 | C | T | 1 | a0001c0001t0005g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159-19738G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107041930 | |||||||
| chr12:107042218 | A | C | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-20026T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042218 | |||||||
| chr12:107042229 | C | A | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-20037G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042229 | |||||||
| chr12:107042247 | T | C | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159-20055A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042247 | |||||||
| chr12:107042408 | C | T | 1 | a0001c0001t0002g0257 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.159-20216G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042408 | |||||||
| chr12:107042498 | T | C | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-20306A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042498 | |||||||
| chr12:107042556 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.159-20364A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042556 | |||||||
| chr12:107042561 | G | A | 6 | a0001c0001t0004g0160 a0001c0001t0004g0166 a0001c0001t0004g0167 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-20369C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042561 | |||||||
| chr12:107042571 | C | T | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-20379G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042571 | |||||||
| chr12:107042596 | T | C | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159-20404A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042596 | |||||||
| chr12:107042607 | AG | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-20416delC | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107042607 | |||||||
| chr12:107043028 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-20836G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043028 | |||||||
| chr12:107043049 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0117 |
3 | HG00735.hp2 HG01070.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.159-20857C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043049 | |||||||
| chr12:107043070 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.159-20878A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043070 | |||||||
| chr12:107043075 | C | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00597.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.159-20883G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043075 | |||||||
| chr12:107043233 | T | A | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.159-21041A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043233 | |||||||
| chr12:107043483 | C | T | 1 | a0001c0002t0003g0211 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.159-21291G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043483 | |||||||
| chr12:107043644 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.159-21452A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043644 | |||||||
| chr12:107043647 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.159-21455G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043647 | |||||||
| chr12:107043818 | G | A | 2 | a0001c0002t0003g0012 a0001c0002t0003g0221 |
3 | NA18975.hp2 NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.159-21626C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043818 | |||||||
| chr12:107043834 | TAC | T | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-21644_159-2164 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107043834 | |||||||
| chr12:107044289 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.159-22097C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044289 | |||||||
| chr12:107044300 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.159-22108T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044300 | |||||||
| chr12:107044359 | C | T | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.159-22167G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044359 | |||||||
| chr12:107044396 | C | A | 1 | a0001c0001t0001g0060 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.159-22204G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044396 | |||||||
| chr12:107044603 | A | G | 1 | a0001c0002t0003g0215 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.159-22411T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044603 | |||||||
| chr12:107044793 | A | G | 2 | a0001c0002t0003g0199 a0001c0002t0003g0208 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.159-22601T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044793 | |||||||
| chr12:107044856 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-22664G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107044856 | |||||||
| chr12:107045248 | T | A | 5 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(2): Show |
6 | HG01243.hp2 HG02280.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-23056A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045248 | |||||||
| chr12:107045381 | C | T | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-23189G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045381 | |||||||
| chr12:107045441 | T | G | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-23249A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045441 | |||||||
| chr12:107045475 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.159-23283A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045475 | |||||||
| chr12:107045544 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0117 |
3 | HG00735.hp2 HG01070.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.159-23352C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045544 | |||||||
| chr12:107045582 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0131 |
2 | HG01361.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.159-23390G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045582 | |||||||
| chr12:107045583 | G | A | 6 | a0001c0001t0002g0234 a0001c0001t0002g0247 a0001c0001t0002g0254 others(3): Show |
6 | HG00673.hp1 HG01978.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-23391C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045583 | |||||||
| chr12:107045688 | G | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-23496C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045688 | |||||||
| chr12:107045705 | C | T | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-23513G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045705 | |||||||
| chr12:107045740 | T | G | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-23548A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045740 | |||||||
| chr12:107045753 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.159-23561C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045753 | |||||||
| chr12:107045756 | C | A | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159-23564G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045756 | |||||||
| chr12:107045768 | T | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-23576A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045768 | |||||||
| chr12:107045823 | C | T | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159-23631G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045823 | |||||||
| chr12:107045882 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.159-23690G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045882 | |||||||
| chr12:107045985 | G | C | 1 | a0001c0002t0003g0186 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.159-23793C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107045985 | |||||||
| chr12:107046125 | TA | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.159-23934delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046125 | |||||||
| chr12:107046292 | CA | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
180 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.159-24101delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046292 | |||||||
| chr12:107046352 | T | C | 3 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG01167.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.159-24160A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046352 | |||||||
| chr12:107046367 | C | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.159-24175G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046367 | |||||||
| chr12:107046525 | C | T | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.159-24333G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046525 | |||||||
| chr12:107046644 | C | T | 3 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 |
3 | HG02818.hp1 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.159-24452G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046644 | |||||||
| chr12:107046675 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.159-24483T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046675 | |||||||
| chr12:107046820 | T | C | 1 | a0001c0001t0002g0265 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.159-24628A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107046820 | |||||||
| chr12:107047046 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.159-24854G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047046 | |||||||
| chr12:107047085 | T | C | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-24893A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047085 | |||||||
| chr12:107047129 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.159-24937T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047129 | |||||||
| chr12:107047156 | A | C | 3 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0013g0173 |
4 | HG01884.hp1 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-24964T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047156 | |||||||
| chr12:107047576 | T | C | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-25384A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047576 | |||||||
| chr12:107047583 | A | G | 1 | a0001c0002t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.159-25391T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047583 | |||||||
| chr12:107047683 | T | A | 1 | a0001c0001t0001g0031 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.159-25491A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047683 | |||||||
| chr12:107047764 | A | C | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.159-25572T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047764 | |||||||
| chr12:107047768 | C | T | 1 | a0001c0001t0002g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.159-25576G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047768 | |||||||
| chr12:107047774 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.159-25582T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107047774 | |||||||
| chr12:107048087 | A | AT | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-25896dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048087 | |||||||
| chr12:107048169 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.159-25977G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048169 | |||||||
| chr12:107048326 | C | A | 3 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-26134G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048326 | |||||||
| chr12:107048355 | C | T | 1 | a0001c0002t0012g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.159-26163G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048355 | |||||||
| chr12:107048364 | G | A | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-26172C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048364 | |||||||
| chr12:107048425 | A | T | 3 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-26233T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048425 | |||||||
| chr12:107048505 | T | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-26313A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048505 | |||||||
| chr12:107048537 | C | T | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.159-26345G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048537 | |||||||
| chr12:107048878 | C | T | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-26686G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048878 | |||||||
| chr12:107048982 | A | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-26790T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107048982 | |||||||
| chr12:107049237 | A | G | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.159-27045T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049237 | |||||||
| chr12:107049521 | C | T | 2 | a0001c0001t0002g0297 a0001c0001t0002g0298 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.159-27329G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049521 | |||||||
| chr12:107049589 | C | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-27397G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049589 | |||||||
| chr12:107049629 | C | T | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-27437G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049629 | |||||||
| chr12:107049676 | A | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-27484T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049676 | |||||||
| chr12:107049762 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-27570A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049762 | |||||||
| chr12:107049768 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
157 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.159-27576A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049768 | |||||||
| chr12:107049997 | G | A | 1 | a0001c0001t0004g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.159-27805C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107049997 | |||||||
| chr12:107050374 | G | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-28182C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050374 | |||||||
| chr12:107050375 | G | C | 1 | a0001c0001t0010g0051 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.159-28183C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050375 | |||||||
| chr12:107050428 | C | T | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-28236G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050428 | |||||||
| chr12:107050443 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.159-28251C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050443 | |||||||
| chr12:107050449 | A | G | 1 | a0001c0001t0004g0157 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.159-28257T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050449 | |||||||
| chr12:107050488 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.159-28296G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050488 | |||||||
| chr12:107050805 | C | T | 6 | a0001c0002t0003g0182 a0001c0002t0003g0183 a0001c0002t0003g0189 others(3): Show |
6 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-28613G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050805 | |||||||
| chr12:107050897 | G | C | 2 | a0001c0002t0003g0203 a0001c0002t0003g0214 |
2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.159-28705C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050897 | |||||||
| chr12:107050943 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0033 others(15): Show |
19 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.159-28751C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107050943 | |||||||
| chr12:107051050 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.159-28858C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107051050 | |||||||
| chr12:107051317 | T | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.159-29125A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107051317 | |||||||
| chr12:107051359 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.159-29167A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107051359 | |||||||
| chr12:107051882 | C | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
179 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.159-29690G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107051882 | |||||||
| chr12:107051952 | A | ATTGTC | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-29761_159-2976 others(9): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107051952 | |||||||
| chr12:107052103 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.159-29911C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052103 | |||||||
| chr12:107052183 | ATACCCAG others(2): Show |
A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
98 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.159-30000_159-2999 others(13): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052183 | |||||||
| chr12:107052199 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
98 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.159-30007T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052199 | |||||||
| chr12:107052250 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.159-30058T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052250 | |||||||
| chr12:107052641 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.159-30449A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052641 | |||||||
| chr12:107052804 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
264 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.159-30612A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052804 | |||||||
| chr12:107052828 | G | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG00639.hp1 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-30636C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107052828 | |||||||
| chr12:107053063 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-30871G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053063 | |||||||
| chr12:107053129 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.159-30937C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053129 | |||||||
| chr12:107053214 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0069 |
4 | HG01516.hp1 HG04199.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-31022A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053214 | |||||||
| chr12:107053333 | T | C | 6 | a0001c0001t0004g0160 a0001c0001t0004g0166 a0001c0001t0004g0167 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-31141A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053333 | |||||||
| chr12:107053387 | G | T | 6 | a0001c0001t0004g0160 a0001c0001t0004g0166 a0001c0001t0004g0167 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.159-31195C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053387 | |||||||
| chr12:107053446 | A | G | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-31254T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053446 | |||||||
| chr12:107053561 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.159-31369C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053561 | |||||||
| chr12:107053573 | C | T | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-31381G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053573 | |||||||
| chr12:107053691 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.159-31499A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053691 | |||||||
| chr12:107053864 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01256.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.159-31672T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053864 | |||||||
| chr12:107053964 | G | C | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-31772C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107053964 | |||||||
| chr12:107054555 | C | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
232 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.159-32363G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054555 | |||||||
| chr12:107054587 | C | T | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-32395G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054587 | |||||||
| chr12:107054650 | G | GA | 12 | a0001c0001t0001g0085 a0001c0001t0001g0098 a0001c0001t0001g0150 others(9): Show |
12 | HG02257.hp2 HG02602.hp1 HG04228.hp2 others(9): Show |
intron_variant | MODIFIER | c.159-32459dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054650 | |||||||
| chr12:107054663 | A | G | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.159-32471T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054663 | |||||||
| chr12:107054763 | C | T | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-32571G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054763 | |||||||
| chr12:107054845 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-32653C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107054845 | |||||||
| chr12:107055213 | T | C | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.159-33021A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107055213 | |||||||
| chr12:107055401 | T | C | 2 | a0001c0001t0002g0257 a0001c0001t0002g0258 |
2 | NA18949.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.159-33209A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107055401 | |||||||
| chr12:107055634 | T | C | 5 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02630.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-33442A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107055634 | |||||||
| chr12:107055639 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.159-33447A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107055639 | |||||||
| chr12:107055972 | T | C | 2 | a0001c0001t0007g0029 a0001c0001t0007g0030 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.159-33780A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107055972 | |||||||
| chr12:107056049 | G | A | 5 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(2): Show |
6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-33857C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056049 | |||||||
| chr12:107056336 | G | C | 9 | a0001c0001t0002g0246 a0001c0001t0002g0259 a0001c0001t0002g0260 others(6): Show |
9 | HG01123.hp1 HG01433.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.159-34144C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056336 | |||||||
| chr12:107056400 | A | G | 1 | a0001c0001t0005g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159-34208T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056400 | |||||||
| chr12:107056415 | C | G | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-34223G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056415 | |||||||
| chr12:107056580 | C | CT | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(73): Show |
78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.159-34389dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056580 | |||||||
| chr12:107056606 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.159-34414T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056606 | |||||||
| chr12:107056689 | G | A | 1 | a0001c0002t0003g0197 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.159-34497C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056689 | |||||||
| chr12:107056974 | T | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.159-34782A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107056974 | |||||||
| chr12:107057088 | A | C | 1 | a0001c0001t0002g0302 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.159-34896T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057088 | |||||||
| chr12:107057096 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.159-34904C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057096 | |||||||
| chr12:107057220 | A | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.159-35028T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057220 | |||||||
| chr12:107057456 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.159-35264A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057456 | |||||||
| chr12:107057495 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.159-35303G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057495 | |||||||
| chr12:107057592 | G | A | 1 | a0001c0002t0003g0204 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.158+35212C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057592 | |||||||
| chr12:107057875 | A | T | 1 | a0001c0002t0003g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.158+34929T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107057875 | |||||||
| chr12:107058292 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+34512T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058292 | |||||||
| chr12:107058309 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.158+34495G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058309 | |||||||
| chr12:107058359 | A | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+34445T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058359 | |||||||
| chr12:107058538 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+34266C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058538 | |||||||
| chr12:107058685 | T | C | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+34119A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058685 | |||||||
| chr12:107058717 | G | A | 1 | a0001c0002t0003g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.158+34087C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107058717 | |||||||
| chr12:107059007 | C | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(31): Show |
36 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.158+33797G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059007 | |||||||
| chr12:107059248 | T | C | 3 | a0001c0001t0002g0233 a0001c0001t0002g0263 a0001c0001t0002g0300 |
3 | HG02257.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.158+33556A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059248 | |||||||
| chr12:107059254 | TTTTG | T | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+33546_158+3354 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059254 | |||||||
| chr12:107059261 | T | C | 3 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0002g0302 |
3 | HG02602.hp1 NA18943.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.158+33543A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059261 | |||||||
| chr12:107059272 | AACAGGGT others(8): Show |
A | 1 | a0001c0001t0001g0148 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+33517_158+3353 others(19): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059272 | |||||||
| chr12:107059278 | G | T | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+33526C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059278 | |||||||
| chr12:107059578 | G | A | 2 | a0001c0001t0002g0241 a0001c0001t0002g0267 |
2 | HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.158+33226C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107059578 | |||||||
| chr12:107060078 | A | T | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
81 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.158+32726T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060078 | |||||||
| chr12:107060079 | T | G | 83 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(80): Show |
86 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.158+32725A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060079 | |||||||
| chr12:107060081 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.158+32723G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060081 | |||||||
| chr12:107060082 | G | A | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
81 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.158+32722C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060082 | |||||||
| chr12:107060196 | T | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+32608A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060196 | |||||||
| chr12:107060282 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.158+32522C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060282 | |||||||
| chr12:107060343 | C | T | 3 | a0001c0002t0003g0175 a0001c0002t0003g0176 a0001c0002t0003g0209 |
3 | HG01361.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.158+32461G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060343 | |||||||
| chr12:107060374 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.158+32430A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060374 | |||||||
| chr12:107060488 | T | C | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+32316A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060488 | |||||||
| chr12:107060519 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.158+32285A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060519 | |||||||
| chr12:107060712 | C | T | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.158+32092G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060712 | |||||||
| chr12:107060737 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+32067A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060737 | |||||||
| chr12:107060997 | A | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+31807T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107060997 | |||||||
| chr12:107061005 | T | G | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+31799A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061005 | |||||||
| chr12:107061307 | A | G | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+31497T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061307 | |||||||
| chr12:107061311 | C | G | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+31493G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061311 | |||||||
| chr12:107061318 | A | T | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+31486T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061318 | |||||||
| chr12:107061363 | T | C | 2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG02300.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.158+31441A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061363 | |||||||
| chr12:107061541 | G | A | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+31263C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061541 | |||||||
| chr12:107061590 | C | G | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+31214G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061590 | |||||||
| chr12:107061677 | C | T | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+31127G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061677 | |||||||
| chr12:107061678 | G | A | 1 | a0001c0001t0002g0281 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.158+31126C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061678 | |||||||
| chr12:107061712 | T | C | 1 | a0001c0001t0007g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158+31092A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061712 | |||||||
| chr12:107061811 | A | T | 5 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0168 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+30993T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061811 | |||||||
| chr12:107061826 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.158+30978A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107061826 | |||||||
| chr12:107062025 | CA | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
253 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.158+30778delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062025 | |||||||
| chr12:107062033 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0002g0267 a0001c0002t0003g0208 |
2 | HG02683.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.158+30751_158+3077 others(24): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062033 | |||||||
| chr12:107062041 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
155 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.158+30763T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062041 | |||||||
| chr12:107062130 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
263 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.158+30674C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062130 | |||||||
| chr12:107062165 | A | T | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+30639T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062165 | |||||||
| chr12:107062215 | T | C | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(73): Show |
78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.158+30589A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062215 | |||||||
| chr12:107062322 | T | A | 3 | a0001c0002t0003g0190 a0001c0002t0003g0206 a0001c0002t0003g0212 |
3 | HG02027.hp1 NA18963.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.158+30482A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062322 | |||||||
| chr12:107062468 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.158+30336G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107062468 | |||||||
| chr12:107063009 | C | A | 1 | a0001c0001t0002g0245 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.158+29795G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063009 | |||||||
| chr12:107063181 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.158+29623G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063181 | |||||||
| chr12:107063367 | T | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+29437A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063367 | |||||||
| chr12:107063434 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+29370A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063434 | |||||||
| chr12:107063469 | A | C | 2 | a0001c0001t0002g0246 a0001c0001t0002g0273 |
2 | HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.158+29335T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063469 | |||||||
| chr12:107063550 | G | A | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.158+29254C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063550 | |||||||
| chr12:107063599 | T | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+29205A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063599 | |||||||
| chr12:107063828 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.158+28976G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107063828 | |||||||
| chr12:107064060 | T | C | 6 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(3): Show |
7 | HG01243.hp2 HG01884.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+28744A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064060 | |||||||
| chr12:107064114 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.158+28690T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064114 | |||||||
| chr12:107064115 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+28689G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064115 | |||||||
| chr12:107064120 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.158+28684C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064120 | |||||||
| chr12:107064125 | G | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+28679C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064125 | |||||||
| chr12:107064168 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.158+28636C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064168 | |||||||
| chr12:107064400 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.158+28404C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064400 | |||||||
| chr12:107064634 | TTAGAAA | T | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(73): Show |
78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.158+28164_158+2816 others(10): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064634 | |||||||
| chr12:107064778 | C | T | 1 | a0001c0002t0003g0207 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.158+28026G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064778 | |||||||
| chr12:107064905 | A | C | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+27899T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064905 | |||||||
| chr12:107064941 | A | T | 1 | a0001c0001t0004g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.158+27863T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064941 | |||||||
| chr12:107064998 | AT | A | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+27805delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107064998 | |||||||
| chr12:107065026 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.158+27778C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065026 | |||||||
| chr12:107065164 | C | T | 5 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0168 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+27640G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065164 | |||||||
| chr12:107065318 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.158+27486G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065318 | |||||||
| chr12:107065390 | T | G | 2 | a0001c0001t0002g0238 a0001c0001t0002g0284 |
2 | HG02132.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.158+27414A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065390 | |||||||
| chr12:107065465 | C | G | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+27339G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065465 | |||||||
| chr12:107065487 | C | T | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+27317G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107065487 | |||||||
| chr12:107066063 | T | C | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+26741A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066063 | |||||||
| chr12:107066120 | C | T | 61 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(58): Show |
63 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.158+26684G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066120 | |||||||
| chr12:107066405 | T | G | 1 | a0001c0001t0002g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.158+26399A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066405 | |||||||
| chr12:107066537 | C | T | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+26267G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066537 | |||||||
| chr12:107066711 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.158+26093C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066711 | |||||||
| chr12:107066711 | G | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+26093C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066711 | |||||||
| chr12:107066820 | G | C | 1 | a0001c0002t0003g0196 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.158+25984C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066820 | |||||||
| chr12:107066935 | G | A | 1 | a0001c0001t0002g0281 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.158+25869C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107066935 | |||||||
| chr12:107067124 | T | C | 1 | a0001c0001t0005g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158+25680A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067124 | |||||||
| chr12:107067184 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0070 |
3 | HG02683.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.158+25620C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067184 | |||||||
| chr12:107067441 | T | C | 1 | a0001c0001t0014g0270 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.158+25363A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067441 | |||||||
| chr12:107067563 | C | CA | 19 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0002g0289 others(16): Show |
21 | HG00673.hp2 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.158+25240dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067563 | |||||||
| chr12:107067865 | T | C | 1 | a0001c0002t0012g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.158+24939A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067865 | |||||||
| chr12:107067983 | C | T | 73 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(70): Show |
75 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.158+24821G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107067983 | |||||||
| chr12:107068147 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.158+24657C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107068147 | |||||||
| chr12:107068254 | G | T | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+24550C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107068254 | |||||||
| chr12:107068457 | C | T | 1 | a0001c0002t0003g0179 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.158+24347G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107068457 | |||||||
| chr12:107068604 | T | C | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+24200A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107068604 | |||||||
| chr12:107068972 | G | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.158+23832C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107068972 | |||||||
| chr12:107069033 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.158+23771T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069033 | |||||||
| chr12:107069226 | AT | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
168 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.158+23577delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069226 | |||||||
| chr12:107069256 | G | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+23548C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069256 | |||||||
| chr12:107069350 | G | A | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+23454C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069350 | |||||||
| chr12:107069352 | G | A | 7 | a0001c0002t0003g0175 a0001c0002t0003g0176 a0001c0002t0003g0199 others(4): Show |
7 | HG01361.hp2 HG02622.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+23452C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069352 | |||||||
| chr12:107069414 | A | G | 1 | a0001c0002t0003g0174 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.158+23390T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069414 | |||||||
| chr12:107069574 | G | GTA | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+23228_158+2322 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069574 | |||||||
| chr12:107069574 | G | GTATATAT others(8): Show |
1 | a0001c0001t0003g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.158+23215_158+2322 others(19): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069574 | |||||||
| chr12:107069583 | TAAAGTAT others(23): Show |
T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.158+23191_158+2322 others(34): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069583 | |||||||
| chr12:107069585 | A | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+23219T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069585 | |||||||
| chr12:107069604 | A | ATATATAT others(6): Show |
76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(73): Show |
79 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.158+23199_158+2320 others(17): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069604 | |||||||
| chr12:107069604 | A | ATATATAT others(49): Show |
1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+23199_158+2320 others(60): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069604 | |||||||
| chr12:107069611 | TAA | T | 14 | a0001c0001t0001g0131 a0001c0001t0001g0149 a0001c0001t0001g0150 others(11): Show |
15 | HG01884.hp1 HG01981.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.158+23191_158+2319 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069611 | |||||||
| chr12:107069612 | AAAAAGTA others(22): Show |
A | 1 | a0001c0001t0001g0132 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.158+23163_158+2319 others(33): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069612 | |||||||
| chr12:107069613 | A | AAGTATAT others(4): Show |
1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+23190_158+2319 others(15): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069613 | |||||||
| chr12:107069613 | A | T | 131 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(128): Show |
138 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.158+23191T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069613 | |||||||
| chr12:107069614 | AAAGT | A | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+23186_158+2318 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069614 | |||||||
| chr12:107069619 | A | G | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+23185T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069619 | |||||||
| chr12:107069620 | T | TATATATA others(8): Show |
2 | a0001c0001t0003g0013 a0001c0001t0003g0193 |
3 | HG02572.hp1 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.158+23183_158+2318 others(19): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069620 | |||||||
| chr12:107069643 | A | T | 1 | a0001c0002t0003g0184 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.158+23161T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069643 | |||||||
| chr12:107069647 | G | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+23157C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069647 | |||||||
| chr12:107069713 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.158+23091A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069713 | |||||||
| chr12:107069785 | C | T | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+23019G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069785 | |||||||
| chr12:107069947 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA18973.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.158+22857G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107069947 | |||||||
| chr12:107070549 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.158+22255T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070549 | |||||||
| chr12:107070551 | GAAAGA | G | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+22248_158+2225 others(9): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070551 | |||||||
| chr12:107070589 | T | C | 1 | a0001c0001t0004g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.158+22215A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070589 | |||||||
| chr12:107070666 | T | TTTTA | 33 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0022 others(30): Show |
34 | HG00639.hp2 HG01928.hp2 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.158+22134_158+2213 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070666 | |||||||
| chr12:107070666 | T | TTTTATTT others(1): Show |
5 | a0001c0001t0002g0232 a0001c0001t0002g0293 a0001c0001t0011g0240 others(2): Show |
5 | HG01943.hp1 HG02155.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+22130_158+2213 others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070666 | |||||||
| chr12:107070666 | TTTTA | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(64): Show |
72 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.158+22134_158+2213 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070666 | |||||||
| chr12:107070666 | TTTTATTT others(1): Show |
T | 10 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(7): Show |
11 | HG00140.hp2 HG00642.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.158+22130_158+2213 others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070666 | |||||||
| chr12:107070666 | TTTTATTT others(5): Show |
T | 6 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.158+22126_158+2213 others(16): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070666 | |||||||
| chr12:107070761 | C | T | 1 | a0001c0003t0006g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.158+22043G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070761 | |||||||
| chr12:107070803 | G | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+22001C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070803 | |||||||
| chr12:107070867 | AT | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0118 a0001c0001t0002g0298 others(4): Show |
8 | HG01081.hp2 HG01934.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.158+21936delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070867 | |||||||
| chr12:107070867 | ATT | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
256 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.158+21935_158+2193 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070867 | |||||||
| chr12:107070917 | G | A | 1 | a0001c0001t0004g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.158+21887C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070917 | |||||||
| chr12:107070984 | G | A | 1 | a0001c0002t0003g0197 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.158+21820C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070984 | |||||||
| chr12:107070993 | A | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
252 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.158+21811T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070993 | |||||||
| chr12:107070993 | A | T | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+21811T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107070993 | |||||||
| chr12:107071118 | C | G | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+21686G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107071118 | |||||||
| chr12:107071635 | A | C | 3 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+21169T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107071635 | |||||||
| chr12:107071851 | G | A | 2 | a0001c0001t0004g0007 a0001c0001t0004g0157 |
3 | HG02280.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.158+20953C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107071851 | |||||||
| chr12:107072175 | ACCTTT | A | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+20624_158+2062 others(9): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072175 | |||||||
| chr12:107072177 | CTTTCT | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.158+20622_158+2062 others(9): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072177 | |||||||
| chr12:107072194 | T | C | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+20610A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072194 | |||||||
| chr12:107072439 | C | T | 103 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(100): Show |
108 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(105): Show |
intron_variant | MODIFIER | c.158+20365G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072439 | |||||||
| chr12:107072664 | T | C | 1 | a0001c0001t0002g0299 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.158+20140A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072664 | |||||||
| chr12:107072794 | C | T | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+20010G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072794 | |||||||
| chr12:107072920 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.158+19884G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072920 | |||||||
| chr12:107072921 | T | G | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+19883A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072921 | |||||||
| chr12:107072923 | A | G | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+19881T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107072923 | |||||||
| chr12:107073023 | G | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG00639.hp1 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+19781C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073023 | |||||||
| chr12:107073082 | AAAT | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
98 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.158+19719_158+1972 others(7): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073082 | |||||||
| chr12:107073104 | C | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+19700G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073104 | |||||||
| chr12:107073138 | TGGGAAAG others(2): Show |
T | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+19657_158+1966 others(13): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073138 | |||||||
| chr12:107073243 | C | CT | 7 | a0001c0001t0001g0099 a0001c0001t0004g0007 a0001c0001t0004g0157 others(4): Show |
8 | HG02280.hp1 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.158+19560dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073243 | |||||||
| chr12:107073243 | C | CTCT | 9 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(6): Show |
10 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.158+19560_158+1956 others(7): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073243 | |||||||
| chr12:107073328 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.158+19476C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073328 | |||||||
| chr12:107073424 | A | T | 1 | a0001c0001t0002g0297 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.158+19380T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073424 | |||||||
| chr12:107073426 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.158+19378G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073426 | |||||||
| chr12:107073497 | A | G | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+19307T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073497 | |||||||
| chr12:107073498 | G | A | 1 | a0001c0002t0003g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.158+19306C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073498 | |||||||
| chr12:107073723 | A | AGTCC | 3 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+19077_158+1908 others(8): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073723 | |||||||
| chr12:107073728 | G | A | 1 | a0001c0002t0012g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.158+19076C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073728 | |||||||
| chr12:107073907 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.158+18897C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073907 | |||||||
| chr12:107073935 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.158+18869T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107073935 | |||||||
| chr12:107074051 | T | A | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+18753A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074051 | |||||||
| chr12:107074058 | T | C | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+18746A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074058 | |||||||
| chr12:107074108 | A | G | 6 | a0001c0001t0004g0160 a0001c0001t0004g0166 a0001c0001t0004g0167 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+18696T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074108 | |||||||
| chr12:107074369 | A | T | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+18435T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074369 | |||||||
| chr12:107074477 | G | C | 1 | a0001c0002t0003g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.158+18327C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074477 | |||||||
| chr12:107074483 | A | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(36): Show |
40 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.158+18321T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074483 | |||||||
| chr12:107074501 | T | A | 2 | a0001c0002t0003g0014 a0001c0002t0003g0215 |
3 | HG03490.hp1 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.158+18303A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074501 | |||||||
| chr12:107074562 | A | T | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+18242T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074562 | |||||||
| chr12:107074678 | C | T | 1 | a0001c0001t0007g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158+18126G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074678 | |||||||
| chr12:107074749 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.158+18055A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074749 | |||||||
| chr12:107074753 | G | A | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+18051C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074753 | |||||||
| chr12:107074786 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0096 others(2): Show |
6 | HG00408.hp2 NA18944.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+18018C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074786 | |||||||
| chr12:107074787 | G | A | 3 | a0001c0002t0003g0216 a0001c0002t0003g0217 a0001c0002t0003g0218 |
3 | HG01074.hp1 HG01255.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.158+18017C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107074787 | |||||||
| chr12:107075015 | C | CA | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
130 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.158+17788dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075015 | |||||||
| chr12:107075015 | C | CAA | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0098 others(35): Show |
41 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.158+17787_158+1778 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075015 | |||||||
| chr12:107075087 | C | T | 1 | a0001c0002t0003g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.158+17717G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075087 | |||||||
| chr12:107075157 | T | C | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+17647A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075157 | |||||||
| chr12:107075162 | CA | C | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+17641delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075162 | |||||||
| chr12:107075168 | T | G | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+17636A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075168 | |||||||
| chr12:107075190 | A | G | 7 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 others(4): Show |
7 | HG01099.hp2 HG01256.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+17614T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075190 | |||||||
| chr12:107075544 | G | C | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.158+17260C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075544 | |||||||
| chr12:107075670 | G | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
8 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.158+17134C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075670 | |||||||
| chr12:107075928 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.158+16876A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075928 | |||||||
| chr12:107075994 | G | A | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+16810C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107075994 | |||||||
| chr12:107076081 | C | A | 2 | a0001c0001t0002g0238 a0001c0001t0002g0284 |
2 | HG02132.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.158+16723G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076081 | |||||||
| chr12:107076103 | G | T | 1 | a0001c0001t0007g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.158+16701C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076103 | |||||||
| chr12:107076337 | G | A | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+16467C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076337 | |||||||
| chr12:107076370 | G | A | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+16434C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076370 | |||||||
| chr12:107076618 | GA | G | 25 | a0001c0001t0001g0023 a0001c0001t0002g0278 a0001c0001t0002g0281 others(22): Show |
27 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.158+16185delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076618 | |||||||
| chr12:107076618 | GAA | G | 80 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(77): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+16184_158+1618 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076618 | |||||||
| chr12:107076634 | A | C | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+16170T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076634 | |||||||
| chr12:107076695 | A | G | 2 | a0001c0001t0011g0239 a0001c0001t0011g0240 |
2 | HG02155.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.158+16109T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076695 | |||||||
| chr12:107076746 | G | A | 2 | a0001c0001t0003g0013 a0001c0001t0003g0193 |
3 | HG02572.hp1 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.158+16058C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076746 | |||||||
| chr12:107076770 | G | A | 3 | a0001c0001t0003g0013 a0001c0001t0003g0192 a0001c0001t0003g0193 |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+16034C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076770 | |||||||
| chr12:107076792 | G | A | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+16012C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076792 | |||||||
| chr12:107076811 | C | T | 3 | a0001c0001t0002g0238 a0001c0001t0002g0284 a0001c0001t0002g0295 |
3 | HG00558.hp2 HG02132.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.158+15993G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076811 | |||||||
| chr12:107076977 | C | T | 11 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(8): Show |
12 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+15827G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107076977 | |||||||
| chr12:107077066 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.158+15738A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077066 | |||||||
| chr12:107077100 | C | T | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+15704G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077100 | |||||||
| chr12:107077117 | TCA | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG02083.hp1 NA18612.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.158+15685_158+1568 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077117 | |||||||
| chr12:107077162 | A | AAC | 14 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(11): Show |
16 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.158+15640_158+1564 others(6): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077162 | |||||||
| chr12:107077291 | T | C | 2 | a0001c0001t0004g0164 a0001c0001t0004g0165 |
2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.158+15513A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077291 | |||||||
| chr12:107077530 | T | C | 1 | a0001c0002t0003g0219 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.158+15274A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077530 | |||||||
| chr12:107077579 | T | C | 2 | a0001c0002t0003g0189 a0001c0002t0003g0220 |
2 | HG02145.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.158+15225A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077579 | |||||||
| chr12:107077604 | T | A | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+15200A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077604 | |||||||
| chr12:107077653 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.158+15151A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077653 | |||||||
| chr12:107077694 | G | C | 4 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0002g0281 others(1): Show |
4 | HG02602.hp1 NA18943.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+15110C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077694 | |||||||
| chr12:107077777 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.158+15027G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077777 | |||||||
| chr12:107077786 | A | G | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+15018T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077786 | |||||||
| chr12:107077826 | C | G | 1 | a0001c0001t0002g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.158+14978G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107077826 | |||||||
| chr12:107078015 | G | A | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+14789C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078015 | |||||||
| chr12:107078286 | C | T | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+14518G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078286 | |||||||
| chr12:107078428 | A | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.158+14376T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078428 | |||||||
| chr12:107078516 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+14288G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078516 | |||||||
| chr12:107078809 | T | G | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.158+13995A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078809 | |||||||
| chr12:107078844 | T | G | 1 | a0001c0002t0003g0221 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.158+13960A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078844 | |||||||
| chr12:107078926 | T | C | 1 | a0001c0001t0004g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.158+13878A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078926 | |||||||
| chr12:107078929 | C | T | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+13875G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078929 | |||||||
| chr12:107078950 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+13854C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078950 | |||||||
| chr12:107078954 | T | A | 1 | a0001c0001t0004g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.158+13850A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107078954 | |||||||
| chr12:107079099 | A | AG | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+13704dupC | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079099 | |||||||
| chr12:107079141 | A | T | 2 | a0001c0001t0005g0225 a0001c0001t0005g0227 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.158+13663T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079141 | |||||||
| chr12:107079276 | G | A | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+13528C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079276 | |||||||
| chr12:107079426 | CA | C | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+13377delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079426 | |||||||
| chr12:107079660 | G | T | 1 | a0001c0001t0002g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.158+13144C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079660 | |||||||
| chr12:107079662 | C | T | 1 | a0001c0001t0002g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.158+13142G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079662 | |||||||
| chr12:107079766 | T | C | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+13038A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107079766 | |||||||
| chr12:107080184 | G | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+12620C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080184 | |||||||
| chr12:107080365 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | NA18950.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.158+12439G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080365 | |||||||
| chr12:107080649 | T | TA | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0159 others(1): Show |
5 | HG02027.hp2 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+12154dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080649 | |||||||
| chr12:107080742 | G | C | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+12062C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080742 | |||||||
| chr12:107080872 | A | G | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+11932T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080872 | |||||||
| chr12:107080888 | T | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+11916A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107080888 | |||||||
| chr12:107081026 | A | C | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+11778T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081026 | |||||||
| chr12:107081030 | G | A | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+11774C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081030 | |||||||
| chr12:107081440 | T | C | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+11364A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081440 | |||||||
| chr12:107081527 | G | A | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.158+11277C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081527 | |||||||
| chr12:107081531 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.158+11273A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081531 | |||||||
| chr12:107081954 | C | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
260 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.158+10850G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107081954 | |||||||
| chr12:107082087 | A | T | 1 | a0001c0001t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.158+10717T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082087 | |||||||
| chr12:107082213 | G | C | 81 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(78): Show |
83 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+10591C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082213 | |||||||
| chr12:107082333 | C | T | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+10471G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082333 | |||||||
| chr12:107082474 | C | T | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+10330G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082474 | |||||||
| chr12:107082475 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+10329C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082475 | |||||||
| chr12:107082521 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.158+10283C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082521 | |||||||
| chr12:107082845 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.158+9959C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082845 | |||||||
| chr12:107082864 | C | G | 42 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.158+9940G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082864 | |||||||
| chr12:107082920 | A | C | 2 | a0001c0001t0002g0283 a0001c0004t0002g0282 |
2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.158+9884T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082920 | |||||||
| chr12:107082938 | T | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(33): Show |
38 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.158+9866A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107082938 | |||||||
| chr12:107083021 | TCCCTCAG others(2): Show |
T | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+9774_158+9782d others(11): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083021 | |||||||
| chr12:107083089 | T | C | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+9715A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083089 | |||||||
| chr12:107083234 | T | A | 1 | a0001c0001t0001g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.158+9570A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083234 | |||||||
| chr12:107083448 | A | G | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+9356T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083448 | |||||||
| chr12:107083450 | A | G | 3 | a0001c0001t0002g0236 a0001c0001t0002g0283 a0001c0004t0002g0282 |
3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.158+9354T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083450 | |||||||
| chr12:107083595 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9209G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083595 | |||||||
| chr12:107083596 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9208T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083596 | |||||||
| chr12:107083603 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9201A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083603 | |||||||
| chr12:107083621 | G | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+9183C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083621 | |||||||
| chr12:107083626 | G | C | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9178C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083626 | |||||||
| chr12:107083627 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9177C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083627 | |||||||
| chr12:107083641 | C | G | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9163G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083641 | |||||||
| chr12:107083642 | C | T | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+9162G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083642 | |||||||
| chr12:107083643 | G | C | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+9161C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083643 | |||||||
| chr12:107083742 | A | G | 1 | a0001c0001t0007g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158+9062T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083742 | |||||||
| chr12:107083743 | T | C | 7 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
7 | HG01361.hp1 HG01981.hp2 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.158+9061A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083743 | |||||||
| chr12:107083745 | G | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.158+9059C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083745 | |||||||
| chr12:107083746 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.158+9058C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083746 | |||||||
| chr12:107083946 | C | T | 5 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+8858G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107083946 | |||||||
| chr12:107084196 | GA | G | 2 | a0001c0001t0004g0007 a0001c0001t0004g0157 |
3 | HG02280.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.158+8607delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084196 | |||||||
| chr12:107084337 | T | G | 2 | a0001c0001t0002g0283 a0001c0004t0002g0282 |
2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.158+8467A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084337 | |||||||
| chr12:107084810 | A | G | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+7994T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084810 | |||||||
| chr12:107084909 | T | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+7895A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084909 | |||||||
| chr12:107084915 | T | C | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+7889A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084915 | |||||||
| chr12:107084973 | C | CA | 28 | a0001c0001t0001g0033 a0001c0001t0001g0133 a0001c0001t0001g0134 others(25): Show |
31 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.158+7830dupT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084973 | |||||||
| chr12:107084973 | CA | C | 8 | a0001c0001t0002g0235 a0001c0001t0002g0296 a0001c0001t0004g0009 others(5): Show |
9 | HG01884.hp1 HG02145.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.158+7830delT | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084973 | |||||||
| chr12:107084986 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.158+7818T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107084986 | |||||||
| chr12:107085065 | GC | G | 7 | a0001c0002t0003g0010 a0001c0002t0003g0174 a0001c0002t0003g0184 others(4): Show |
8 | NA18953.hp2 NA18956.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.158+7738delG | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085065 | |||||||
| chr12:107085141 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.158+7663C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085141 | |||||||
| chr12:107085235 | C | T | 1 | a0001c0001t0007g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158+7569G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085235 | |||||||
| chr12:107085270 | C | T | 2 | a0001c0002t0003g0182 a0001c0002t0003g0183 |
2 | HG00099.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.158+7534G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085270 | |||||||
| chr12:107085273 | C | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+7531G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085273 | |||||||
| chr12:107085277 | C | G | 1 | a0001c0001t0001g0033 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.158+7527G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085277 | |||||||
| chr12:107085648 | C | G | 6 | a0001c0001t0004g0160 a0001c0001t0004g0166 a0001c0001t0004g0167 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+7156G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085648 | |||||||
| chr12:107085730 | T | C | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+7074A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085730 | |||||||
| chr12:107085747 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+7057G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107085747 | |||||||
| chr12:107086354 | G | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+6450C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086354 | |||||||
| chr12:107086400 | TAAAAGAG others(4): Show |
T | 4 | a0001c0002t0003g0178 a0001c0002t0003g0179 a0001c0002t0003g0180 others(1): Show |
4 | HG00735.hp1 HG01069.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+6393_158+6403d others(13): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086400 | |||||||
| chr12:107086437 | G | A | 5 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(2): Show |
6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.158+6367C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086437 | |||||||
| chr12:107086677 | G | A | 76 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(73): Show |
78 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.158+6127C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086677 | |||||||
| chr12:107086698 | A | G | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+6106T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086698 | |||||||
| chr12:107086766 | C | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+6038G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086766 | |||||||
| chr12:107086809 | A | ATTCTACT others(3): Show |
1 | a0001c0001t0002g0234 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.158+5985_158+5994d others(12): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086809 | |||||||
| chr12:107086872 | G | A | 1 | a0001c0002t0003g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.158+5932C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086872 | |||||||
| chr12:107086879 | G | A | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+5925C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107086879 | |||||||
| chr12:107087179 | A | G | 1 | a0001c0001t0005g0224 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158+5625T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087179 | |||||||
| chr12:107087289 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.158+5515A>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087289 | |||||||
| chr12:107087373 | A | G | 2 | a0001c0002t0003g0175 a0001c0002t0003g0176 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.158+5431T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087373 | |||||||
| chr12:107087511 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.158+5293A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087511 | |||||||
| chr12:107087635 | T | C | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+5169A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087635 | |||||||
| chr12:107087673 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.158+5131C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087673 | |||||||
| chr12:107087811 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+4993C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087811 | |||||||
| chr12:107087837 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.158+4967G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107087837 | |||||||
| chr12:107088027 | A | T | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG02257.hp2 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+4777T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088027 | |||||||
| chr12:107088072 | C | T | 1 | a0001c0002t0012g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.158+4732G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088072 | |||||||
| chr12:107088356 | G | C | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+4448C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088356 | |||||||
| chr12:107088393 | C | G | 1 | a0001c0001t0015g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.158+4411G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088393 | |||||||
| chr12:107088492 | AG | A | 15 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(12): Show |
17 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.158+4311delC | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088492 | |||||||
| chr12:107088606 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.158+4198C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088606 | |||||||
| chr12:107088622 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.158+4182A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088622 | |||||||
| chr12:107088683 | G | C | 1 | a0001c0001t0005g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.158+4121C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088683 | |||||||
| chr12:107088691 | A | G | 3 | a0001c0001t0008g0156 a0001c0001t0008g0171 a0001c0001t0008g0172 |
3 | HG01884.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+4113T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088691 | |||||||
| chr12:107088792 | C | T | 1 | a0001c0002t0003g0174 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.158+4012G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088792 | |||||||
| chr12:107088812 | G | A | 11 | a0001c0001t0004g0009 a0001c0001t0004g0160 a0001c0001t0004g0163 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+3992C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088812 | |||||||
| chr12:107088889 | A | G | 78 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0229 others(75): Show |
80 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.158+3915T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107088889 | |||||||
| chr12:107089029 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.158+3775A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089029 | |||||||
| chr12:107089189 | T | A | 4 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0298 others(1): Show |
4 | HG03195.hp1 HG03579.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+3615A>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089189 | |||||||
| chr12:107089373 | T | TC | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
259 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.158+3430_158+3431i others(3): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089373 | |||||||
| chr12:107089375 | C | A | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+3429G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089375 | |||||||
| chr12:107089401 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.158+3403G>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089401 | |||||||
| chr12:107089537 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.158+3267T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089537 | |||||||
| chr12:107089646 | C | T | 3 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 |
3 | HG02818.hp1 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.158+3158G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089646 | |||||||
| chr12:107089647 | G | A | 1 | a0001c0001t0002g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.158+3157C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089647 | |||||||
| chr12:107089798 | A | C | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+3006T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089798 | |||||||
| chr12:107089860 | C | A | 3 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0159 |
4 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+2944G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107089860 | |||||||
| chr12:107090041 | C | T | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+2763G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090041 | |||||||
| chr12:107090074 | C | T | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+2730G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090074 | |||||||
| chr12:107090096 | C | CT | 18 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0157 others(15): Show |
20 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.158+2707dupA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090096 | |||||||
| chr12:107090110 | G | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
151 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.158+2694C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090110 | |||||||
| chr12:107090295 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.158+2509T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090295 | |||||||
| chr12:107090320 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00597.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.158+2484C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090320 | |||||||
| chr12:107090337 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.158+2467G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090337 | |||||||
| chr12:107090423 | G | T | 1 | a0001c0001t0002g0232 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.158+2381C>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090423 | |||||||
| chr12:107090600 | C | T | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+2204G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090600 | |||||||
| chr12:107090872 | G | GAAC | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+1929_158+1931d others(5): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090872 | |||||||
| chr12:107090901 | C | T | 5 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(2): Show |
6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.158+1903G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090901 | |||||||
| chr12:107090960 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.158+1844T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107090960 | |||||||
| chr12:107091007 | A | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(5): Show |
9 | HG02056.hp2 HG02155.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.158+1797T>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091007 | |||||||
| chr12:107091039 | T | C | 3 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 |
3 | HG02723.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.158+1765A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091039 | |||||||
| chr12:107091045 | CT | C | 5 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(2): Show |
7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+1758delA | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091045 | |||||||
| chr12:107091056 | T | C | 3 | a0001c0003t0006g0008 a0001c0003t0006g0161 a0001c0003t0006g0162 |
4 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+1748A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091056 | |||||||
| chr12:107091103 | G | C | 1 | a0001c0001t0002g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.158+1701C>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091103 | |||||||
| chr12:107091188 | C | T | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+1616G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091188 | |||||||
| chr12:107091191 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.158+1613G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091191 | |||||||
| chr12:107091362 | A | G | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+1442T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091362 | |||||||
| chr12:107091433 | C | T | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+1371G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091433 | |||||||
| chr12:107091445 | T | C | 1 | a0001c0001t0005g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158+1359A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091445 | |||||||
| chr12:107091488 | GCTT | G | 5 | a0001c0001t0004g0009 a0001c0001t0004g0163 a0001c0001t0004g0164 others(2): Show |
6 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.158+1313_158+1315d others(5): Show |
CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091488 | |||||||
| chr12:107091657 | T | C | 1 | a0001c0001t0002g0302 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.158+1147A>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091657 | |||||||
| chr12:107091775 | A | G | 2 | a0001c0001t0004g0007 a0001c0001t0004g0157 |
3 | HG02280.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.158+1029T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091775 | |||||||
| chr12:107091781 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01256.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.158+1023G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091781 | |||||||
| chr12:107091807 | G | A | 5 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0168 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+997C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107091807 | |||||||
| chr12:107092197 | C | T | 4 | a0001c0001t0004g0007 a0001c0001t0004g0157 a0001c0001t0004g0158 others(1): Show |
5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+607G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092197 | |||||||
| chr12:107092210 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.158+594G>A | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092210 | |||||||
| chr12:107092265 | A | G | 2 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.158+539T>C | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092265 | |||||||
| chr12:107092290 | C | A | 2 | a0001c0001t0008g0171 a0001c0001t0008g0172 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+514G>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092290 | |||||||
| chr12:107092555 | A | C | 1 | a0001c0001t0008g0156 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.158+249T>G | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092555 | |||||||
| chr12:107092729 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.158+75C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092729 | |||||||
| chr12:107092791 | G | A | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.158+13C>T | CRY1 | ENSG00000008405.12 | transcript | ENST00000008527.10 | protein_coding | 1/12 | chr12 | 107092791 |