Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8454 |
| ensemblid | ENSG00000055130.18 |
| hgncid | 2551 |
| symbol | CUL1 |
| name | cullin 1 |
| refseq_nuc | NM_003592.3 |
| refseq_prot | NP_003583.2 |
| ensembl_nuc | ENST00000325222.9 |
| ensembl_prot | ENSP00000326804.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 148698903 |
| end | 148801110 |
| strand | + |
| ver | v1.2 |
| region | chr7:148698903-148801110 |
| region5000 | chr7:148693903-148806110 |
| regionname0 | CUL1_chr7_148698903_148801110 |
| regionname5000 | CUL1_chr7_148693903_148806110 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2328 | 318 | 87 | 70 | 117 | 10 | 32 | CUL1_chr7_148693903_148806110 | CUL1 | ATGTC others(2323): Show |
chr7 | 148693903 | 148806110 | ||
| a0001c0002 | 0/0 | 2328 | 13 | 0 | 0 | 13 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | ATGTC others(2323): Show |
chr7 | 148693903 | 148806110 | ||
| a0001c0003 | 0/0 | 2328 | 5 | 5 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | ATGTC others(2323): Show |
chr7 | 148693903 | 148806110 | ||
| a0001c0004 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | ATGTC others(2323): Show |
chr7 | 148693903 | 148806110 | ||
| a0001c0005 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | ATGTC others(2323): Show |
chr7 | 148693903 | 148806110 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3147 | 307 | 78 | 68 | 117 | 10 | 32 | CUL1_chr7_148693903_148806110 | CUL1 | AGGCG others(3142): Show |
chr7 | 148693903 | 148806110 |
| a0001c0001t0002 | 0/0 | 3147 | 9 | 8 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | AGGCG others(3142): Show |
chr7 | 148693903 | 148806110 |
| a0001c0001t0003 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | AGGCG others(3142): Show |
chr7 | 148693903 | 148806110 |
| a0001c0001t0004 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | AGGCG others(3142): Show |
chr7 | 148693903 | 148806110 |
| a0001c0002t0001 | 0/0 | 3147 | 13 | 0 | 0 | 13 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | AGGCG others(3142): Show |
chr7 | 148693903 | 148806110 |
| a0001c0003t0001 | 0/0 | 3147 | 5 | 5 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | AGGCG others(3142): Show |
chr7 | 148693903 | 148806110 |
| a0001c0004t0001 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | AGGCG others(3142): Show |
chr7 | 148693903 | 148806110 |
| a0001c0005t0001 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | AGGCG others(3142): Show |
chr7 | 148693903 | 148806110 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0003t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| a0001c0005t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | GBR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0323 | EUR | FIN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00408 | hp1 | a0001 | c0005 | t0001 | g0256 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | CHS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0129 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | CDX | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02165 | hp1 | a0001 | c0004 | t0001 | g0211 | EAS | CDX | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0309 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0109 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0108 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | STU | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | YRI | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ASW | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ASW | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | USA | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | USA | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0040 | REF | REF | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0177 | REF | REF | CUL1_chr7_148693903_148806110 | CUL1 | chr7 | 148693903 | 148806110 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:148730239 | G | A | 1 | a0001c0004 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.117G>A | p.Lys39Lys | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/22 | 405/3147 | 117/2331 | 39/776 | chr7 | 148730239 | |||
| chr7:148787021 | C | T | 1 | a0001c0005 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.1380C>T | p.Asp460Asp | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/22 | 1668/3147 | 1380/2331 | 460/776 | chr7 | 148787021 | |||
| chr7:148792728 | G | A | 2 | a0001c0002 a0001c0005 |
14 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.1809G>A | p.Ala603Ala | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/22 | 2097/3147 | 1809/2331 | 603/776 | chr7 | 148792728 | |||
| chr7:148799283 | C | T | 1 | a0001c0003 | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.2145C>T | p.Ile715Ile | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/22 | 2433/3147 | 2145/2331 | 715/776 | chr7 | 148799283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:148698983 | C | T | 1 | a0001c0001t0002 | 9 | HG00735.hp1 HG01884.hp2 HG02723.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-208C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/22 | 31140 | chr7 | 148698983 | ||||||
| chr7:148800595 | G | T | 1 | a0001c0001t0004 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 13 | chr7 | 148800595 | ||||||
| chr7:148800671 | T | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 89 | chr7 | 148800671 | ||||||
| chr7:148800683 | A | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 101 | chr7 | 148800683 | ||||||
| chr7:148800684 | C | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 102 | chr7 | 148800684 | ||||||
| chr7:148800685 | C | A | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 103 | chr7 | 148800685 | ||||||
| chr7:148800694 | A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 112 | chr7 | 148800694 | ||||||
| chr7:148800696 | A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 114 | chr7 | 148800696 | ||||||
| chr7:148800697 | A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 115 | chr7 | 148800697 | ||||||
| chr7:148800698 | A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 116 | chr7 | 148800698 | ||||||
| chr7:148800699 | C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 117 | chr7 | 148800699 | ||||||
| chr7:148800701 | G | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 119 | chr7 | 148800701 | ||||||
| chr7:148800702 | A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 120 | chr7 | 148800702 | ||||||
| chr7:148800705 | C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 123 | chr7 | 148800705 | ||||||
| chr7:148800706 | C | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*124C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 124 | chr7 | 148800706 | ||||||
| chr7:148800710 | A | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 128 | chr7 | 148800710 | ||||||
| chr7:148800711 | C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 129 | chr7 | 148800711 | ||||||
| chr7:148800713 | C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*131C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 131 | chr7 | 148800713 | ||||||
| chr7:148800714 | C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*132C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 132 | chr7 | 148800714 | ||||||
| chr7:148800715 | C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 133 | chr7 | 148800715 | ||||||
| chr7:148800716 | A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 134 | chr7 | 148800716 | ||||||
| chr7:148800718 | C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 136 | chr7 | 148800718 | ||||||
| chr7:148800719 | A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 137 | chr7 | 148800719 | ||||||
| chr7:148800721 | C | A | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 139 | chr7 | 148800721 | ||||||
| chr7:148800723 | G | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 141 | chr7 | 148800723 | ||||||
| chr7:148800726 | C | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 144 | chr7 | 148800726 | ||||||
| chr7:148800731 | A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 149 | chr7 | 148800731 | ||||||
| chr7:148800734 | T | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 152 | chr7 | 148800734 | ||||||
| chr7:148800742 | A | C | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*160A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 160 | chr7 | 148800742 | ||||||
| chr7:148800743 | A | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*161A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 161 | chr7 | 148800743 | ||||||
| chr7:148800749 | C | G | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 167 | chr7 | 148800749 | ||||||
| chr7:148800750 | A | T | 1 | a0001c0001t0003 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 22/22 | 168 | chr7 | 148800750 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:148699061 | A | T | 81 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(78): Show |
81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-162+32A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699061 | |||||||
| chr7:148699206 | C | T | 4 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+177C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699206 | |||||||
| chr7:148699308 | A | G | 1 | a0001c0001t0001g0335 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-162+279A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699308 | |||||||
| chr7:148699457 | G | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
74 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-162+428G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699457 | |||||||
| chr7:148699485 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | NA19072.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-162+456C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699485 | |||||||
| chr7:148699543 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-162+514C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699543 | |||||||
| chr7:148699563 | G | A | 88 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(85): Show |
88 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-162+534G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699563 | |||||||
| chr7:148699684 | G | T | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG02257.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-162+655G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699684 | |||||||
| chr7:148699737 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-162+708C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699737 | |||||||
| chr7:148699753 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-162+724C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699753 | |||||||
| chr7:148699807 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-162+778C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699807 | |||||||
| chr7:148699957 | T | C | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02523.hp2 NA18943.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+928T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699957 | |||||||
| chr7:148699980 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-162+951T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699980 | |||||||
| chr7:148699996 | G | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(2): Show |
5 | HG02056.hp1 NA18953.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+967G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148699996 | |||||||
| chr7:148700141 | A | C | 4 | a0001c0001t0001g0333 a0001c0002t0001g0331 a0001c0002t0001g0332 others(1): Show |
4 | NA18957.hp1 NA18960.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162+1112A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700141 | |||||||
| chr7:148700262 | C | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-162+1233C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700262 | |||||||
| chr7:148700305 | C | G | 1 | a0001c0001t0001g0330 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-162+1276C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700305 | |||||||
| chr7:148700399 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-162+1370A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700399 | |||||||
| chr7:148700745 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG01978.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-162+1716A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700745 | |||||||
| chr7:148700799 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | NA18943.hp1 NA18992.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-162+1770C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148700799 | |||||||
| chr7:148701044 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-162+2015A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701044 | |||||||
| chr7:148701179 | TAACTTA | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
74 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-162+2158_-162+216 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148701179 | ||||||
| chr7:148701208 | G | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
226 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-162+2179G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701208 | |||||||
| chr7:148701216 | T | G | 2 | a0001c0002t0001g0255 a0001c0005t0001g0256 |
2 | HG00408.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-162+2187T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701216 | |||||||
| chr7:148701242 | G | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-162+2213G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701242 | |||||||
| chr7:148701448 | G | T | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(10): Show |
13 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-162+2419G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701448 | |||||||
| chr7:148701541 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+2512G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701541 | |||||||
| chr7:148701542 | T | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(79): Show |
82 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-162+2513T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701542 | |||||||
| chr7:148701616 | G | C | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+2587G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701616 | |||||||
| chr7:148701617 | A | G | 3 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 |
3 | HG02615.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-162+2588A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701617 | |||||||
| chr7:148701677 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-162+2648C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701677 | |||||||
| chr7:148701866 | G | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG02257.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-162+2837G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701866 | |||||||
| chr7:148701872 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0134 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-162+2843C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148701872 | |||||||
| chr7:148702463 | C | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
8 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+3434C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148702463 | |||||||
| chr7:148703079 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-162+4050C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703079 | |||||||
| chr7:148703226 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-162+4197C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703226 | |||||||
| chr7:148703296 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-162+4267G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703296 | |||||||
| chr7:148703374 | A | C | 16 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0313 others(13): Show |
16 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-162+4345A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703374 | |||||||
| chr7:148703521 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-162+4492T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703521 | |||||||
| chr7:148703521 | TTTTTTTG | T | 5 | a0001c0001t0001g0091 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
5 | HG00738.hp2 HG00741.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+4513_-162+451 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148703521 | ||||||
| chr7:148703542 | G | GT | 65 | a0001c0001t0001g0012 a0001c0001t0001g0102 a0001c0001t0001g0103 others(62): Show |
65 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.-162+4521dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148703542 | ||||||
| chr7:148703618 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-162+4589C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703618 | |||||||
| chr7:148703669 | A | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG00558.hp1 HG02523.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+4640A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703669 | |||||||
| chr7:148703718 | G | T | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-162+4689G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703718 | |||||||
| chr7:148703914 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-162+4885A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703914 | |||||||
| chr7:148703990 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+4961G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148703990 | |||||||
| chr7:148704125 | A | G | 1 | a0001c0001t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-162+5096A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704125 | |||||||
| chr7:148704156 | G | GC | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
86 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.-162+5136dupC | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148704156 | ||||||
| chr7:148704156 | G | GCC | 21 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(18): Show |
21 | HG00558.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-162+5135_-162+513 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148704156 | ||||||
| chr7:148704158 | C | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-162+5129C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704158 | |||||||
| chr7:148704159 | C | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0310 a0001c0001t0001g0311 |
3 | HG01952.hp1 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-162+5130C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704159 | |||||||
| chr7:148704316 | G | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
140 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.-162+5287G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704316 | |||||||
| chr7:148704344 | A | G | 1 | a0001c0001t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-162+5315A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704344 | |||||||
| chr7:148704563 | G | A | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+5534G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704563 | |||||||
| chr7:148704577 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-162+5548G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704577 | |||||||
| chr7:148704811 | GTTA | G | 31 | a0001c0001t0001g0092 a0001c0001t0001g0110 a0001c0001t0001g0111 others(28): Show |
31 | HG01952.hp1 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.-162+5788_-162+579 others(7): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148704811 | ||||||
| chr7:148704841 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-162+5812A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148704841 | |||||||
| chr7:148705156 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG03017.hp1 HG03490.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+6127C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148705156 | |||||||
| chr7:148705618 | T | A | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
91 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.-162+6589T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148705618 | |||||||
| chr7:148705686 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+6657A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148705686 | |||||||
| chr7:148705736 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-162+6707A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148705736 | |||||||
| chr7:148705892 | C | G | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
138 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.-162+6863C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148705892 | |||||||
| chr7:148706053 | G | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0258 |
2 | NA18955.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-162+7024G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706053 | |||||||
| chr7:148706077 | T | C | 16 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(13): Show |
16 | HG01952.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-162+7048T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706077 | |||||||
| chr7:148706102 | G | A | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
138 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.-162+7073G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706102 | |||||||
| chr7:148706151 | A | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
89 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-162+7122A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706151 | |||||||
| chr7:148706220 | A | G | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
89 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-162+7191A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706220 | |||||||
| chr7:148706346 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+7317C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706346 | |||||||
| chr7:148706367 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+7338A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706367 | |||||||
| chr7:148706372 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+7343G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706372 | |||||||
| chr7:148706416 | A | G | 2 | a0001c0001t0002g0232 a0001c0001t0002g0233 |
2 | HG00735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-162+7387A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706416 | |||||||
| chr7:148706600 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-162+7571T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706600 | |||||||
| chr7:148706633 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-162+7604A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706633 | |||||||
| chr7:148706673 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-162+7644G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706673 | |||||||
| chr7:148706825 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
134 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.-162+7796T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148706825 | |||||||
| chr7:148707146 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0134 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-162+8117C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707146 | |||||||
| chr7:148707258 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-162+8229G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707258 | |||||||
| chr7:148707287 | G | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): Show |
83 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-162+8258G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707287 | |||||||
| chr7:148707452 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-162+8423A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707452 | |||||||
| chr7:148707585 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-162+8556C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707585 | |||||||
| chr7:148707646 | A | G | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
5 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+8617A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707646 | |||||||
| chr7:148707666 | G | GT | 4 | a0001c0001t0001g0051 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+8638dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148707666 | ||||||
| chr7:148707790 | C | T | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+8761C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707790 | |||||||
| chr7:148707801 | T | C | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+8772T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707801 | |||||||
| chr7:148707804 | T | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
8 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+8775T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707804 | |||||||
| chr7:148707849 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+8820C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707849 | |||||||
| chr7:148707850 | T | G | 54 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0085 others(51): Show |
54 | HG00738.hp2 HG00741.hp2 HG01123.hp2 others(51): Show |
intron_variant | MODIFIER | c.-162+8821T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148707850 | |||||||
| chr7:148708036 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-162+9007G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148708036 | |||||||
| chr7:148708214 | C | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01433.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-162+9185C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148708214 | |||||||
| chr7:148708486 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-162+9457T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148708486 | |||||||
| chr7:148708679 | T | C | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+9650T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148708679 | |||||||
| chr7:148708748 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-162+9719G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148708748 | |||||||
| chr7:148709095 | T | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02109.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-162+10066T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709095 | |||||||
| chr7:148709372 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-162+10343G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709372 | |||||||
| chr7:148709377 | C | G | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+10348C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709377 | |||||||
| chr7:148709445 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+10416G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709445 | |||||||
| chr7:148709455 | C | T | 2 | a0001c0003t0001g0108 a0001c0003t0001g0109 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-162+10426C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709455 | |||||||
| chr7:148709582 | A | C | 15 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(12): Show |
15 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-162+10553A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709582 | |||||||
| chr7:148709615 | A | G | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-162+10586A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709615 | |||||||
| chr7:148709703 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-162+10674G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709703 | |||||||
| chr7:148709767 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-162+10738A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709767 | |||||||
| chr7:148709885 | C | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+10856C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148709885 | |||||||
| chr7:148710143 | C | A | 15 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(12): Show |
15 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-162+11114C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710143 | |||||||
| chr7:148710305 | T | TGGCTC | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
138 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.-162+11276_-162+11 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710305 | |||||||
| chr7:148710307 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-162+11278C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710307 | |||||||
| chr7:148710357 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-162+11328G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710357 | |||||||
| chr7:148710368 | G | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | NA19064.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-162+11339G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710368 | |||||||
| chr7:148710369 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02109.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-162+11340A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710369 | |||||||
| chr7:148710390 | A | G | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-162+11361A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710390 | |||||||
| chr7:148710433 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+11404G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710433 | |||||||
| chr7:148710493 | C | T | 9 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0294 others(6): Show |
9 | HG00408.hp2 HG00642.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+11464C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710493 | |||||||
| chr7:148710721 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+11692C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710721 | |||||||
| chr7:148710807 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-162+11778G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710807 | |||||||
| chr7:148710824 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 |
4 | HG01099.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162+11795C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710824 | |||||||
| chr7:148710831 | T | A | 14 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(11): Show |
14 | HG01952.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-162+11802T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710831 | |||||||
| chr7:148710921 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-162+11892G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148710921 | |||||||
| chr7:148711056 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-162+12027C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711056 | |||||||
| chr7:148711186 | A | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
94 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.-162+12157A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711186 | |||||||
| chr7:148711227 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-162+12198C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711227 | |||||||
| chr7:148711228 | G | C | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-162+12199G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711228 | |||||||
| chr7:148711230 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-162+12201A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711230 | |||||||
| chr7:148711285 | C | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+12256C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711285 | |||||||
| chr7:148711489 | G | A | 5 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
5 | HG01070.hp1 HG01081.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+12460G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711489 | |||||||
| chr7:148711562 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | NA19072.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-162+12533G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711562 | |||||||
| chr7:148711594 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+12565G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711594 | |||||||
| chr7:148711653 | CAG | C | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+12625_-162+12 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711653 | |||||||
| chr7:148711667 | C | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0307 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-162+12638C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711667 | |||||||
| chr7:148711685 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-162+12656A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711685 | |||||||
| chr7:148711927 | C | T | 6 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(3): Show |
6 | HG01928.hp1 HG01934.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+12898C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711927 | |||||||
| chr7:148711991 | T | A | 1 | a0001c0001t0001g0305 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-162+12962T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148711991 | |||||||
| chr7:148712075 | C | A | 5 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | NA18941.hp1 NA18948.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+13046C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712075 | |||||||
| chr7:148712304 | A | G | 15 | a0001c0001t0001g0092 a0001c0001t0001g0110 a0001c0001t0001g0111 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-162+13275A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712304 | |||||||
| chr7:148712475 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-162+13446A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712475 | |||||||
| chr7:148712716 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-162+13687A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712716 | |||||||
| chr7:148712776 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG00408.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-162+13747C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712776 | |||||||
| chr7:148712849 | A | G | 109 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
109 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-162+13820A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712849 | |||||||
| chr7:148712854 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-162+13825T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712854 | |||||||
| chr7:148712990 | G | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+13961G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148712990 | |||||||
| chr7:148713001 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-162+13972T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713001 | |||||||
| chr7:148713031 | A | C | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
94 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.-162+14002A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713031 | |||||||
| chr7:148713300 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-162+14271T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713300 | |||||||
| chr7:148713302 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+14273G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713302 | |||||||
| chr7:148713318 | T | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
8 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+14289T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713318 | |||||||
| chr7:148713378 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-162+14349G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713378 | |||||||
| chr7:148713619 | G | A | 28 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0094 others(25): Show |
28 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.-162+14590G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713619 | |||||||
| chr7:148713735 | A | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0261 |
2 | HG02257.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-162+14706A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713735 | |||||||
| chr7:148713736 | T | TTTTTTGA others(6): Show |
1 | a0001c0002t0001g0334 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-162+14708_-162+14 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148713736 | ||||||
| chr7:148713737 | T | A | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-162+14708T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713737 | |||||||
| chr7:148713754 | C | CA | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+14726dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148713754 | ||||||
| chr7:148713907 | A | G | 9 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-162+14878A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713907 | |||||||
| chr7:148713966 | T | C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
137 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.-162+14937T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713966 | |||||||
| chr7:148713999 | C | T | 6 | a0001c0001t0001g0091 a0001c0001t0001g0237 a0001c0001t0001g0239 others(3): Show |
6 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+14970C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148713999 | |||||||
| chr7:148714549 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-161-15413T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714549 | |||||||
| chr7:148714622 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-161-15340C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714622 | |||||||
| chr7:148714696 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-15266T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714696 | |||||||
| chr7:148714711 | G | A | 12 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0103 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-161-15251G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714711 | |||||||
| chr7:148714717 | A | AT | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
88 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-161-15241dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148714717 | ||||||
| chr7:148714730 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
88 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-161-15232G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714730 | |||||||
| chr7:148714768 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-161-15194C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714768 | |||||||
| chr7:148714793 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-161-15169G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714793 | |||||||
| chr7:148714887 | G | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0237 a0001c0001t0001g0239 others(3): Show |
6 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-15075G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148714887 | |||||||
| chr7:148715011 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0128 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-161-14951A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715011 | |||||||
| chr7:148715279 | A | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
94 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.-161-14683A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715279 | |||||||
| chr7:148715310 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-161-14652G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715310 | |||||||
| chr7:148715360 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-161-14602G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715360 | |||||||
| chr7:148715398 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-161-14564C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715398 | |||||||
| chr7:148715418 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-161-14544T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715418 | |||||||
| chr7:148715421 | A | G | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
138 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.-161-14541A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715421 | |||||||
| chr7:148715429 | C | T | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-14533C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715429 | |||||||
| chr7:148715526 | T | C | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
88 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-161-14436T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715526 | |||||||
| chr7:148715612 | A | C | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-14350A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715612 | |||||||
| chr7:148715789 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-14173T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148715789 | |||||||
| chr7:148716136 | T | TTC | 6 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(3): Show |
6 | HG01928.hp1 HG01934.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-13824_-161-13 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148716136 | ||||||
| chr7:148716191 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-13771A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716191 | |||||||
| chr7:148716340 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-161-13622C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716340 | |||||||
| chr7:148716508 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-161-13454C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716508 | |||||||
| chr7:148716709 | G | A | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
138 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.-161-13253G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716709 | |||||||
| chr7:148716725 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-161-13237C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716725 | |||||||
| chr7:148716885 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-161-13077G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716885 | |||||||
| chr7:148716961 | G | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-13001G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716961 | |||||||
| chr7:148716967 | A | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-161-12995A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716967 | |||||||
| chr7:148716977 | A | G | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG00597.hp2 NA18966.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-161-12985A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148716977 | |||||||
| chr7:148717043 | T | TTTTTG | 15 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0027 others(12): Show |
15 | HG01952.hp1 HG02615.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-161-12888_-161-12 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148717043 | ||||||
| chr7:148717043 | T | TTTTTGTT others(3): Show |
64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
64 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-161-12893_-161-12 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148717043 | ||||||
| chr7:148717043 | T | TTTTTGTT others(8): Show |
1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-161-12898_-161-12 others(21): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148717043 | ||||||
| chr7:148717043 | TTTTTGTT others(3): Show |
T | 1 | a0001c0001t0001g0305 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-161-12893_-161-12 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148717043 | ||||||
| chr7:148717088 | C | A | 5 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | NA18941.hp1 NA18948.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-12874C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717088 | |||||||
| chr7:148717365 | G | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02155.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-161-12597G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717365 | |||||||
| chr7:148717418 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-12544A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717418 | |||||||
| chr7:148717451 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-161-12511C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717451 | |||||||
| chr7:148717489 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-161-12473A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717489 | |||||||
| chr7:148717704 | A | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-12258A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717704 | |||||||
| chr7:148717805 | A | T | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | NA18975.hp1 NA19007.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.-161-12157A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717805 | |||||||
| chr7:148717828 | T | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | NA19072.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-161-12134T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717828 | |||||||
| chr7:148717863 | G | A | 26 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(23): Show |
26 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.-161-12099G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717863 | |||||||
| chr7:148717957 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-161-12005C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148717957 | |||||||
| chr7:148718321 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-161-11641A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148718321 | |||||||
| chr7:148718477 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-161-11485T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148718477 | |||||||
| chr7:148718554 | A | AT | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.-161-11398dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148718554 | ||||||
| chr7:148718648 | T | C | 114 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
114 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-161-11314T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148718648 | |||||||
| chr7:148718718 | AT | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
140 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.-161-11236delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148718718 | ||||||
| chr7:148718819 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-161-11143A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148718819 | |||||||
| chr7:148719012 | G | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.-161-10950G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719012 | |||||||
| chr7:148719316 | A | AT | 15 | a0001c0001t0001g0092 a0001c0001t0001g0110 a0001c0001t0001g0111 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-161-10646_-161-10 others(7): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719316 | |||||||
| chr7:148719316 | A | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0244 |
2 | HG00738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-161-10646A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719316 | |||||||
| chr7:148719642 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-161-10320A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719642 | |||||||
| chr7:148719745 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-161-10217C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719745 | |||||||
| chr7:148719746 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-161-10216G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719746 | |||||||
| chr7:148719764 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-161-10198T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719764 | |||||||
| chr7:148719840 | C | G | 1 | a0001c0001t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-161-10122C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719840 | |||||||
| chr7:148719981 | C | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.-161-9981C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148719981 | |||||||
| chr7:148720059 | A | G | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-9903A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720059 | |||||||
| chr7:148720071 | A | G | 15 | a0001c0001t0001g0092 a0001c0001t0001g0110 a0001c0001t0001g0111 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-161-9891A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720071 | |||||||
| chr7:148720245 | T | C | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-161-9717T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720245 | |||||||
| chr7:148720252 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-161-9710C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720252 | |||||||
| chr7:148720598 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-161-9364A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720598 | |||||||
| chr7:148720662 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-161-9300A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720662 | |||||||
| chr7:148720820 | A | T | 1 | a0001c0001t0001g0212 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-161-9142A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148720820 | |||||||
| chr7:148721034 | T | C | 15 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(12): Show |
15 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-161-8928T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721034 | |||||||
| chr7:148721048 | G | A | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
143 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.-161-8914G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721048 | |||||||
| chr7:148721089 | T | G | 110 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
110 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.-161-8873T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721089 | |||||||
| chr7:148721365 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-161-8597C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721365 | |||||||
| chr7:148721438 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-161-8524T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721438 | |||||||
| chr7:148721463 | T | C | 9 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-161-8499T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721463 | |||||||
| chr7:148721511 | C | T | 1 | a0001c0004t0001g0211 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-161-8451C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721511 | |||||||
| chr7:148721518 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-8444A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721518 | |||||||
| chr7:148721705 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-161-8257G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721705 | |||||||
| chr7:148721709 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-8253A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721709 | |||||||
| chr7:148721724 | C | CT | 11 | a0001c0001t0001g0092 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-161-8229dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148721724 | ||||||
| chr7:148721739 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-8223A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721739 | |||||||
| chr7:148721793 | G | A | 43 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(40): Show |
43 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-161-8169G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721793 | |||||||
| chr7:148721818 | A | G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0073 others(3): Show |
6 | NA18966.hp1 NA18998.hp1 NA19072.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-8144A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721818 | |||||||
| chr7:148721974 | C | T | 43 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(40): Show |
43 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-161-7988C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148721974 | |||||||
| chr7:148722068 | T | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 |
3 | HG02055.hp1 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-161-7894T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722068 | |||||||
| chr7:148722283 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-161-7679C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722283 | |||||||
| chr7:148722379 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-161-7583G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722379 | |||||||
| chr7:148722392 | A | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
56 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-161-7570A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722392 | |||||||
| chr7:148722487 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-7475C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722487 | |||||||
| chr7:148722502 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-161-7460G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722502 | |||||||
| chr7:148722687 | T | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0101 |
3 | HG01123.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-161-7275T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722687 | |||||||
| chr7:148722688 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0101 |
3 | HG01123.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-161-7274T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722688 | |||||||
| chr7:148722690 | C | T | 32 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0094 others(29): Show |
32 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-161-7272C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722690 | |||||||
| chr7:148722955 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0134 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-161-7007A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148722955 | |||||||
| chr7:148723017 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-6945G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723017 | |||||||
| chr7:148723082 | GT | G | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-161-6878delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148723082 | ||||||
| chr7:148723322 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-6640C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723322 | |||||||
| chr7:148723417 | A | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.-161-6545A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723417 | |||||||
| chr7:148723653 | A | G | 11 | a0001c0001t0001g0092 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-161-6309A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723653 | |||||||
| chr7:148723662 | CA | C | 42 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(39): Show |
42 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.-161-6288delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148723662 | ||||||
| chr7:148723662 | CAA | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
101 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.-161-6289_-161-628 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148723662 | ||||||
| chr7:148723743 | C | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-6219C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723743 | |||||||
| chr7:148723774 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-161-6188G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723774 | |||||||
| chr7:148723789 | C | CT | 43 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(40): Show |
43 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-161-6160dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148723789 | ||||||
| chr7:148723789 | C | CTT | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-161-6161_-161-616 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148723789 | ||||||
| chr7:148723801 | T | C | 11 | a0001c0001t0001g0092 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-161-6161T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723801 | |||||||
| chr7:148723997 | T | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0134 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-161-5965T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148723997 | |||||||
| chr7:148724049 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02970.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-5913A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724049 | |||||||
| chr7:148724100 | C | T | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-161-5862C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724100 | |||||||
| chr7:148724436 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0066 |
3 | NA19067.hp2 NA19075.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-161-5526C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724436 | |||||||
| chr7:148724479 | T | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
98 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.-161-5483T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724479 | |||||||
| chr7:148724481 | C | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-5481C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724481 | |||||||
| chr7:148724521 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-5441C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724521 | |||||||
| chr7:148724527 | G | A | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-5435G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724527 | |||||||
| chr7:148724601 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0134 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-161-5361T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724601 | |||||||
| chr7:148724841 | TTTTTTTG others(4): Show |
T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-161-5104_-161-509 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148724841 | ||||||
| chr7:148724904 | A | T | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-161-5058A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148724904 | |||||||
| chr7:148725024 | A | G | 12 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(9): Show |
12 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-161-4938A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725024 | |||||||
| chr7:148725182 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-161-4780C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725182 | |||||||
| chr7:148725198 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-161-4761_-161-475 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725198 | ||||||
| chr7:148725198 | TAC | T | 17 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0091 others(14): Show |
17 | HG00423.hp2 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-161-4751_-161-475 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725198 | ||||||
| chr7:148725202 | C | CACGCAGC others(6): Show |
1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-161-4758_-161-475 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725202 | ||||||
| chr7:148725202 | C | CACGCGCG others(5): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0066 |
2 | NA19067.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-161-4758_-161-475 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725202 | ||||||
| chr7:148725207 | A | ACG | 4 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | NA18943.hp2 NA18961.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-4754_-161-475 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725207 | ||||||
| chr7:148725207 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0070 |
2 | HG03834.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-161-4755A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725207 | |||||||
| chr7:148725209 | A | ACG | 6 | a0001c0001t0001g0205 a0001c0001t0001g0285 a0001c0001t0001g0316 others(3): Show |
6 | HG01081.hp2 HG01109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-4752_-161-475 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725209 | ||||||
| chr7:148725209 | A | G | 84 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
84 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.-161-4753A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725209 | |||||||
| chr7:148725211 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
167 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.-161-4751A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725211 | |||||||
| chr7:148725211 | ACGCGCG | A | 5 | a0001c0001t0001g0137 a0001c0001t0001g0139 a0001c0001t0001g0251 others(2): Show |
5 | HG02258.hp1 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4747_-161-474 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725211 | ||||||
| chr7:148725211 | ACGCGCGC others(3): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-161-4749_-161-474 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725211 | ||||||
| chr7:148725213 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0092 others(3): Show |
6 | HG01978.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-4749G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725213 | |||||||
| chr7:148725214 | C | CGT | 14 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(11): Show |
14 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-161-4747_-161-474 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725214 | ||||||
| chr7:148725215 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0092 others(3): Show |
6 | HG01978.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-4747G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725215 | |||||||
| chr7:148725216 | C | T | 18 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0102 others(15): Show |
18 | HG01952.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-4746C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725216 | |||||||
| chr7:148725217 | G | A | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0092 others(4): Show |
7 | HG01978.hp2 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-161-4745G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725217 | |||||||
| chr7:148725217 | G | GCACACAC others(7): Show |
3 | a0001c0003t0001g0122 a0001c0003t0001g0129 a0001c0003t0001g0309 |
3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-161-4744_-161-474 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725217 | ||||||
| chr7:148725217 | G | GCACGCGC others(17): Show |
1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-161-4744_-161-474 others(28): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725217 | ||||||
| chr7:148725219 | G | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0071 a0001c0001t0001g0072 others(15): Show |
18 | HG01978.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-4743G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725219 | |||||||
| chr7:148725219 | G | GCA | 5 | a0001c0001t0001g0266 a0001c0002t0001g0203 a0001c0002t0001g0331 others(2): Show |
5 | NA18957.hp1 NA18960.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCACACAC others(1): Show |
3 | a0001c0001t0001g0028 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG03490.hp2 HG03492.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCACACAC others(5): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0149 |
2 | HG03710.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCA | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0063 others(2): Show |
5 | HG02155.hp1 HG02523.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACA | 5 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0079 others(2): Show |
5 | HG00558.hp2 HG02109.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACAC others(1): Show |
6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(3): Show |
6 | HG03017.hp1 HG03491.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACAC others(3): Show |
8 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
8 | HG01081.hp1 HG01192.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACAC others(5): Show |
14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0026 others(11): Show |
14 | HG00621.hp1 HG01884.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACAC others(7): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(5): Show |
8 | HG00438.hp2 HG00741.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACAC others(9): Show |
1 | a0001c0001t0001g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACAC others(15): Show |
1 | a0001c0001t0001g0025 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(26): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACAC others(31): Show |
1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(42): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACAC others(35): Show |
1 | a0001c0001t0001g0034 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(46): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACGC others(17): Show |
1 | a0001c0001t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(28): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACGC others(21): Show |
1 | a0001c0001t0001g0012 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(32): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCACGC others(25): Show |
1 | a0001c0001t0001g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(36): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCAC others(3): Show |
1 | a0001c0001t0001g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCAC others(5): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(3): Show |
6 | HG01358.hp2 HG01891.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCAC others(7): Show |
2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCAC others(9): Show |
5 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00639.hp2 HG00738.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCAC others(11): Show |
1 | a0001c0001t0001g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCAC others(13): Show |
1 | a0001c0001t0001g0042 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(24): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCAC others(15): Show |
1 | a0001c0001t0001g0017 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(26): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCAC others(23): Show |
1 | a0001c0001t0001g0016 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(34): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCAC others(33): Show |
1 | a0001c0001t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(44): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCAC others(39): Show |
1 | a0001c0001t0001g0011 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(50): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCGC others(7): Show |
1 | a0001c0001t0001g0008 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCGC others(9): Show |
1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCGC others(15): Show |
1 | a0001c0003t0001g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(26): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCGC others(27): Show |
1 | a0001c0003t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(38): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCGC others(9): Show |
1 | a0001c0001t0001g0066 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCGC others(15): Show |
1 | a0001c0001t0001g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(26): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCGC others(11): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0239 |
2 | HG00738.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-161-4742_-161-474 others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | G | GCGCGCGC others(13): Show |
1 | a0001c0001t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-161-4742_-161-474 others(24): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725219 | GCTCA | G | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
5 | HG01952.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4741_-161-473 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725219 | ||||||
| chr7:148725221 | T | A | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
172 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-161-4741T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725221 | |||||||
| chr7:148725221 | T | G | 45 | a0001c0001t0001g0029 a0001c0001t0001g0068 a0001c0001t0001g0073 others(42): Show |
45 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-161-4741T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725221 | |||||||
| chr7:148725221 | T | TCA | 6 | a0001c0001t0001g0161 a0001c0001t0001g0215 a0001c0001t0001g0230 others(3): Show |
6 | HG01346.hp2 HG01433.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-4715_-161-471 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148725221 | ||||||
| chr7:148725223 | A | G | 20 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0125 others(17): Show |
20 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.-161-4739A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725223 | |||||||
| chr7:148725225 | A | G | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | HG01175.hp2 HG01952.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-4737A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725225 | |||||||
| chr7:148725227 | A | G | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
5 | HG01952.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4735A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725227 | |||||||
| chr7:148725231 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-161-4731A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725231 | |||||||
| chr7:148725247 | A | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(7): Show |
10 | HG00741.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-161-4715A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725247 | |||||||
| chr7:148725248 | C | CA | 3 | a0001c0001t0001g0299 a0001c0001t0001g0323 a0001c0001t0002g0162 |
3 | HG00280.hp2 NA18998.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-161-4714_-161-471 others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725248 | |||||||
| chr7:148725248 | C | CACACACA others(4): Show |
1 | a0001c0001t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-161-4714_-161-471 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725248 | |||||||
| chr7:148725248 | C | CACACACA others(6): Show |
1 | a0001c0001t0001g0073 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-161-4714_-161-471 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725248 | |||||||
| chr7:148725249 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-161-4713C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725249 | |||||||
| chr7:148725260 | T | C | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-4702T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725260 | |||||||
| chr7:148725274 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-161-4688T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725274 | |||||||
| chr7:148725286 | C | T | 11 | a0001c0001t0001g0092 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-161-4676C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725286 | |||||||
| chr7:148725408 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-4554C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725408 | |||||||
| chr7:148725489 | A | G | 5 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
5 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-4473A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725489 | |||||||
| chr7:148725491 | A | T | 1 | a0001c0001t0001g0292 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-161-4471A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725491 | |||||||
| chr7:148725591 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-161-4371C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725591 | |||||||
| chr7:148725815 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-161-4147T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148725815 | |||||||
| chr7:148726254 | T | C | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-3708T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726254 | |||||||
| chr7:148726301 | G | A | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-3661G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726301 | |||||||
| chr7:148726400 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-161-3562A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726400 | |||||||
| chr7:148726468 | C | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
97 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.-161-3494C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726468 | |||||||
| chr7:148726532 | G | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
141 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.-161-3430G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726532 | |||||||
| chr7:148726621 | A | G | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-3341A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726621 | |||||||
| chr7:148726747 | G | C | 1 | a0001c0001t0001g0003 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-161-3215G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726747 | |||||||
| chr7:148726825 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-161-3137A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726825 | |||||||
| chr7:148726833 | C | CA | 28 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0028 others(25): Show |
28 | HG00280.hp2 HG01070.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-161-3112dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148726833 | ||||||
| chr7:148726833 | C | CAA | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
89 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-161-3113_-161-311 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148726833 | ||||||
| chr7:148726850 | AT | A | 11 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0124 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-161-3103delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr7 | 148726850 | ||||||
| chr7:148726851 | T | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
108 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-161-3111T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726851 | |||||||
| chr7:148726852 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-161-3110T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148726852 | |||||||
| chr7:148727090 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-161-2872G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727090 | |||||||
| chr7:148727151 | A | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
98 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.-161-2811A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727151 | |||||||
| chr7:148727155 | A | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
98 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.-161-2807A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727155 | |||||||
| chr7:148727385 | T | C | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-2577T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727385 | |||||||
| chr7:148727449 | T | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0163 |
3 | HG02155.hp2 HG03942.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-161-2513T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727449 | |||||||
| chr7:148727527 | C | T | 5 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0296 others(2): Show |
5 | HG00642.hp2 HG01192.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-2435C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727527 | |||||||
| chr7:148727930 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-161-2032A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727930 | |||||||
| chr7:148727936 | A | G | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
93 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.-161-2026A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727936 | |||||||
| chr7:148727953 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-161-2009C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148727953 | |||||||
| chr7:148728050 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-1912C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728050 | |||||||
| chr7:148728212 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-161-1750C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728212 | |||||||
| chr7:148728250 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-161-1712G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728250 | |||||||
| chr7:148728323 | A | G | 17 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0092 others(14): Show |
17 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-161-1639A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728323 | |||||||
| chr7:148728710 | A | C | 1 | a0001c0001t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-161-1252A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728710 | |||||||
| chr7:148728823 | T | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.-161-1139T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728823 | |||||||
| chr7:148728860 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0034 others(1): Show |
4 | HG02165.hp2 NA18971.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-161-1102A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728860 | |||||||
| chr7:148728876 | G | C | 1 | a0001c0001t0004g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-161-1086G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148728876 | |||||||
| chr7:148729179 | T | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.-161-783T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729179 | |||||||
| chr7:148729224 | T | C | 1 | a0001c0001t0001g0304 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-161-738T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729224 | |||||||
| chr7:148729382 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-161-580C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729382 | |||||||
| chr7:148729580 | A | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
113 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-161-382A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729580 | |||||||
| chr7:148729594 | T | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02615.hp2 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-161-368T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729594 | |||||||
| chr7:148729625 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-161-337T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729625 | |||||||
| chr7:148729628 | C | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-161-334C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729628 | |||||||
| chr7:148729752 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-161-210C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 1/21 | chr7 | 148729752 | |||||||
| chr7:148730342 | A | G | 11 | a0001c0001t0001g0092 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+80A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730342 | |||||||
| chr7:148730378 | A | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG00642.hp1 HG01123.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.140+116A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730378 | |||||||
| chr7:148730381 | G | T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG00597.hp2 NA18966.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.140+119G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730381 | |||||||
| chr7:148730414 | A | G | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+152A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730414 | |||||||
| chr7:148730498 | A | T | 32 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0094 others(29): Show |
32 | HG00738.hp2 HG00741.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.140+236A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730498 | |||||||
| chr7:148730601 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+339T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730601 | |||||||
| chr7:148730644 | A | G | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+382A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730644 | |||||||
| chr7:148730699 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140+437A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730699 | |||||||
| chr7:148730781 | G | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.140+519G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730781 | |||||||
| chr7:148730889 | G | T | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+627G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730889 | |||||||
| chr7:148730900 | T | C | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+638T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148730900 | |||||||
| chr7:148731091 | C | T | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+829C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731091 | |||||||
| chr7:148731196 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140+934C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731196 | |||||||
| chr7:148731393 | A | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG02647.hp1 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.140+1131A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731393 | |||||||
| chr7:148731431 | C | T | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+1169C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731431 | |||||||
| chr7:148731657 | G | A | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+1395G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731657 | |||||||
| chr7:148731658 | A | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+1396A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731658 | |||||||
| chr7:148731801 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.140+1539G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731801 | |||||||
| chr7:148731844 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0128 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.140+1582G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731844 | |||||||
| chr7:148731859 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0146 a0001c0001t0001g0191 others(7): Show |
11 | HG01928.hp2 HG01934.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.140+1597C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148731859 | |||||||
| chr7:148732022 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.140+1760G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732022 | |||||||
| chr7:148732108 | T | C | 3 | a0001c0003t0001g0122 a0001c0003t0001g0129 a0001c0003t0001g0309 |
3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.140+1846T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732108 | |||||||
| chr7:148732261 | G | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+1999G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732261 | |||||||
| chr7:148732320 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.140+2058A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732320 | |||||||
| chr7:148732345 | A | AT | 18 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0064 others(15): Show |
18 | HG00438.hp1 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.140+2101dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148732345 | ||||||
| chr7:148732345 | AT | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(10): Show |
13 | HG01433.hp2 HG01978.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+2101delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148732345 | ||||||
| chr7:148732353 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.140+2091T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732353 | |||||||
| chr7:148732404 | A | G | 1 | a0001c0001t0001g0014 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.140+2142A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732404 | |||||||
| chr7:148732417 | A | G | 2 | a0001c0002t0001g0255 a0001c0005t0001g0256 |
2 | HG00408.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.140+2155A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732417 | |||||||
| chr7:148732434 | C | A | 6 | a0001c0001t0002g0162 a0001c0001t0002g0206 a0001c0001t0002g0207 others(3): Show |
6 | HG01884.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+2172C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732434 | |||||||
| chr7:148732473 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+2211A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732473 | |||||||
| chr7:148732677 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.140+2415G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732677 | |||||||
| chr7:148732714 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
75 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.140+2452G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732714 | |||||||
| chr7:148732719 | G | C | 5 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0327 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+2457G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732719 | |||||||
| chr7:148732970 | C | T | 137 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
137 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.140+2708C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732970 | |||||||
| chr7:148732976 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+2714G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148732976 | |||||||
| chr7:148733027 | G | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.140+2765G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733027 | |||||||
| chr7:148733028 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.140+2766C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733028 | |||||||
| chr7:148733029 | T | G | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.140+2767T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733029 | |||||||
| chr7:148733056 | A | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
93 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.140+2794A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733056 | |||||||
| chr7:148733118 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+2856C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733118 | |||||||
| chr7:148733172 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+2910G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733172 | |||||||
| chr7:148733267 | G | C | 3 | a0001c0001t0002g0164 a0001c0001t0002g0232 a0001c0001t0002g0233 |
3 | HG00735.hp1 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140+3005G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733267 | |||||||
| chr7:148733328 | A | G | 15 | a0001c0001t0001g0092 a0001c0001t0001g0110 a0001c0001t0001g0111 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.140+3066A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733328 | |||||||
| chr7:148733545 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0188 |
2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.140+3283G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733545 | |||||||
| chr7:148733661 | G | GC | 11 | a0001c0001t0001g0092 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+3400dupC | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148733661 | ||||||
| chr7:148733865 | T | A | 1 | a0001c0001t0004g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.140+3603T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148733865 | |||||||
| chr7:148734036 | AAAAAG | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
87 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.140+3789_140+3793d others(7): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148734036 | ||||||
| chr7:148734218 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.140+3956A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148734218 | |||||||
| chr7:148734251 | C | CTG | 5 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
5 | HG00738.hp2 HG00741.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+4001_140+4002d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148734251 | ||||||
| chr7:148734269 | CAG | C | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+4010_140+4011d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148734269 | ||||||
| chr7:148734375 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.140+4113C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148734375 | |||||||
| chr7:148734517 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.140+4255G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148734517 | |||||||
| chr7:148734666 | C | T | 11 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+4404C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148734666 | |||||||
| chr7:148735118 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.140+4856G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735118 | |||||||
| chr7:148735203 | C | T | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG02647.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+4941C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735203 | |||||||
| chr7:148735253 | C | T | 11 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+4991C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735253 | |||||||
| chr7:148735369 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5107C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735369 | |||||||
| chr7:148735370 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5108T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735370 | |||||||
| chr7:148735372 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5110C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735372 | |||||||
| chr7:148735374 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5112G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735374 | |||||||
| chr7:148735375 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5113C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735375 | |||||||
| chr7:148735377 | A | T | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5115A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735377 | |||||||
| chr7:148735379 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5117C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735379 | |||||||
| chr7:148735386 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5124T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735386 | |||||||
| chr7:148735387 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5125T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735387 | |||||||
| chr7:148735395 | A | AGAGCTGT others(4): Show |
1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5133_140+5134i others(13): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735395 | |||||||
| chr7:148735399 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5137T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735399 | |||||||
| chr7:148735407 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5145T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735407 | |||||||
| chr7:148735423 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5161A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735423 | |||||||
| chr7:148735425 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5163G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735425 | |||||||
| chr7:148735426 | A | C | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5164A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735426 | |||||||
| chr7:148735428 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5166C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735428 | |||||||
| chr7:148735433 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+5171C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735433 | |||||||
| chr7:148735442 | A | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
98 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.140+5180A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735442 | |||||||
| chr7:148735443 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5181G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735443 | |||||||
| chr7:148735444 | T | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5182T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735444 | |||||||
| chr7:148735445 | G | T | 11 | a0001c0001t0001g0092 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+5183G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735445 | |||||||
| chr7:148735447 | T | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5185T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735447 | |||||||
| chr7:148735453 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5191G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735453 | |||||||
| chr7:148735454 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.140+5192G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735454 | |||||||
| chr7:148735455 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.140+5193C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735455 | |||||||
| chr7:148735458 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5196C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735458 | |||||||
| chr7:148735460 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5198T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735460 | |||||||
| chr7:148735464 | T | A | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.140+5202T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735464 | |||||||
| chr7:148735469 | C | T | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+5207C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735469 | |||||||
| chr7:148735517 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.140+5255A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735517 | |||||||
| chr7:148735866 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.140+5604C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735866 | |||||||
| chr7:148735924 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.140+5662G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148735924 | |||||||
| chr7:148736007 | T | TA | 7 | a0001c0001t0001g0091 a0001c0001t0001g0167 a0001c0001t0001g0168 others(4): Show |
7 | HG01074.hp1 HG01074.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.140+5765dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148736007 | ||||||
| chr7:148736007 | TA | T | 14 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(11): Show |
14 | HG01070.hp1 HG01070.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.140+5765delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148736007 | ||||||
| chr7:148736007 | TAAA | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(121): Show |
124 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.140+5763_140+5765d others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148736007 | ||||||
| chr7:148736007 | TAAAA | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0090 others(10): Show |
13 | HG01168.hp1 HG02109.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+5762_140+5765d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148736007 | ||||||
| chr7:148736486 | A | G | 3 | a0001c0003t0001g0122 a0001c0003t0001g0129 a0001c0003t0001g0309 |
3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.140+6224A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736486 | |||||||
| chr7:148736542 | G | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.140+6280G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736542 | |||||||
| chr7:148736624 | T | G | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0170 others(1): Show |
4 | HG00280.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+6362T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736624 | |||||||
| chr7:148736781 | A | C | 1 | a0001c0003t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.140+6519A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736781 | |||||||
| chr7:148736971 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.140+6709G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736971 | |||||||
| chr7:148736996 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.140+6734G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148736996 | |||||||
| chr7:148737130 | A | C | 15 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(12): Show |
15 | HG01952.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.140+6868A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737130 | |||||||
| chr7:148737189 | A | AT | 6 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0083 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+6941dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737189 | ||||||
| chr7:148737269 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.140+7007G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737269 | |||||||
| chr7:148737359 | C | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+7097C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737359 | |||||||
| chr7:148737402 | T | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
98 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.140+7140T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737402 | |||||||
| chr7:148737508 | G | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
98 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.140+7246G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737508 | |||||||
| chr7:148737560 | A | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0327 a0001c0001t0001g0328 others(6): Show |
9 | HG02145.hp1 HG02165.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.140+7298A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737560 | |||||||
| chr7:148737571 | T | TATA | 8 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0242 others(5): Show |
8 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+7309_140+7310i others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737571 | |||||||
| chr7:148737572 | T | A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
215 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.140+7310T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737572 | |||||||
| chr7:148737574 | T | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02165.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.140+7312T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737574 | |||||||
| chr7:148737574 | T | TATA | 8 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0242 others(5): Show |
8 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+7312_140+7313i others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737574 | |||||||
| chr7:148737576 | A | ATATT | 43 | a0001c0001t0001g0091 a0001c0001t0001g0154 a0001c0001t0001g0155 others(40): Show |
43 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.140+7352_140+7355d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | ||||||
| chr7:148737576 | A | ATATTTAT others(1): Show |
12 | a0001c0001t0001g0238 a0001c0001t0001g0263 a0001c0001t0001g0264 others(9): Show |
12 | HG00423.hp2 HG01891.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.140+7348_140+7355d others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | ||||||
| chr7:148737576 | A | T | 25 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0204 others(22): Show |
25 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.140+7314A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737576 | |||||||
| chr7:148737576 | ATATT | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
79 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.140+7352_140+7355d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | ||||||
| chr7:148737576 | ATATTTAT others(1): Show |
A | 46 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0092 others(43): Show |
46 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.140+7348_140+7355d others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | ||||||
| chr7:148737576 | ATATTTAT others(5): Show |
A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0290 |
2 | HG02135.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.140+7344_140+7355d others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | ||||||
| chr7:148737576 | ATATTTAT others(13): Show |
A | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.140+7336_140+7355d others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148737576 | ||||||
| chr7:148737578 | A | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02165.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.140+7316A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737578 | |||||||
| chr7:148737580 | T | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG02165.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.140+7318T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737580 | |||||||
| chr7:148737789 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.140+7527C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737789 | |||||||
| chr7:148737806 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.140+7544C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148737806 | |||||||
| chr7:148738005 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.140+7743C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738005 | |||||||
| chr7:148738183 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.140+7921A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738183 | |||||||
| chr7:148738247 | A | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.140+7985A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738247 | |||||||
| chr7:148738301 | A | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.140+8039A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738301 | |||||||
| chr7:148738334 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+8072G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738334 | |||||||
| chr7:148738557 | G | A | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+8295G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738557 | |||||||
| chr7:148738683 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+8421A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738683 | |||||||
| chr7:148738969 | G | A | 3 | a0001c0001t0002g0164 a0001c0001t0002g0232 a0001c0001t0002g0233 |
3 | HG00735.hp1 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140+8707G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148738969 | |||||||
| chr7:148739014 | G | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
93 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.140+8752G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739014 | |||||||
| chr7:148739346 | G | T | 1 | a0001c0001t0001g0315 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.140+9084G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739346 | |||||||
| chr7:148739369 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.140+9107A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739369 | |||||||
| chr7:148739375 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.140+9113T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739375 | |||||||
| chr7:148739417 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.140+9155A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739417 | |||||||
| chr7:148739437 | C | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+9175C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739437 | |||||||
| chr7:148739449 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+9187A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739449 | |||||||
| chr7:148739491 | C | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+9229C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739491 | |||||||
| chr7:148739662 | T | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02109.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.140+9400T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739662 | |||||||
| chr7:148739876 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.140+9614C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739876 | |||||||
| chr7:148739894 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.140+9632A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739894 | |||||||
| chr7:148739912 | C | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.140+9650C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148739912 | |||||||
| chr7:148740058 | C | CT | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
95 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.140+9809dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148740058 | ||||||
| chr7:148740113 | C | T | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
93 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.140+9851C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148740113 | |||||||
| chr7:148740197 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140+9935C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148740197 | |||||||
| chr7:148740255 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.140+9993A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148740255 | |||||||
| chr7:148740391 | T | C | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+10129T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148740391 | |||||||
| chr7:148740940 | A | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.140+10678A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148740940 | |||||||
| chr7:148741053 | C | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
102 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.140+10791C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741053 | |||||||
| chr7:148741180 | CT | C | 139 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
139 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.140+10923delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148741180 | ||||||
| chr7:148741191 | T | TA | 7 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
7 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.140+10930dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148741191 | ||||||
| chr7:148741432 | T | G | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.140+11170T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741432 | |||||||
| chr7:148741444 | TTTAC | T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(73): Show |
76 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.140+11190_140+1119 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148741444 | ||||||
| chr7:148741497 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.140+11235G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741497 | |||||||
| chr7:148741541 | CGATTCTC others(128): Show |
C | 136 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
136 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.140+11323_140+1145 others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148741541 | ||||||
| chr7:148741563 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.140+11301C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741563 | |||||||
| chr7:148741574 | A | G | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.140+11312A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741574 | |||||||
| chr7:148741585 | T | C | 79 | a0001c0001t0001g0067 a0001c0001t0001g0079 a0001c0001t0001g0080 others(76): Show |
79 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.140+11323T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741585 | |||||||
| chr7:148741698 | C | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+11436C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741698 | |||||||
| chr7:148741710 | A | G | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0264 |
3 | HG01978.hp2 HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140+11448A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741710 | |||||||
| chr7:148741712 | C | T | 15 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0205 others(12): Show |
15 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.140+11450C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741712 | |||||||
| chr7:148741832 | C | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0071 others(2): Show |
5 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+11570C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741832 | |||||||
| chr7:148741870 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.140+11608G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148741870 | |||||||
| chr7:148742029 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.140+11767T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742029 | |||||||
| chr7:148742117 | T | A | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+11855T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742117 | |||||||
| chr7:148742182 | T | G | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.141-11794T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742182 | |||||||
| chr7:148742273 | G | C | 212 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(209): Show |
212 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.141-11703G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742273 | |||||||
| chr7:148742282 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.141-11694G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742282 | |||||||
| chr7:148742350 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.141-11626T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742350 | |||||||
| chr7:148742424 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0004g0126 |
3 | HG01891.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.141-11552G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742424 | |||||||
| chr7:148742589 | C | G | 1 | a0001c0001t0001g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.141-11387C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742589 | |||||||
| chr7:148742598 | G | GT | 10 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0183 others(7): Show |
10 | HG01081.hp2 HG01928.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-11360dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | ||||||
| chr7:148742598 | G | GTTTTTTT others(2): Show |
45 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(42): Show |
45 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.141-11368_141-1136 others(13): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | ||||||
| chr7:148742598 | G | GTTTTTTT others(3): Show |
35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(32): Show |
35 | HG00438.hp2 HG00639.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.141-11369_141-1136 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | ||||||
| chr7:148742598 | G | GTTTTTTT others(4): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0064 a0001c0001t0001g0066 others(1): Show |
4 | HG01361.hp2 HG03927.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-11370_141-1136 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | ||||||
| chr7:148742598 | G | GTTTTTTT others(5): Show |
2 | a0001c0001t0001g0239 a0001c0001t0001g0244 |
2 | HG00738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.141-11371_141-1136 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | ||||||
| chr7:148742598 | GT | G | 19 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(16): Show |
19 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.141-11360delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | ||||||
| chr7:148742598 | GTT | G | 35 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 others(32): Show |
35 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.141-11361_141-1136 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148742598 | ||||||
| chr7:148742659 | G | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
88 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.141-11317G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742659 | |||||||
| chr7:148742705 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0071 others(2): Show |
5 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-11271G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742705 | |||||||
| chr7:148742722 | C | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-11254C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742722 | |||||||
| chr7:148742759 | G | T | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-11217G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742759 | |||||||
| chr7:148742807 | T | G | 3 | a0001c0001t0001g0067 a0001c0002t0001g0255 a0001c0005t0001g0256 |
3 | HG00408.hp1 HG00621.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.141-11169T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148742807 | |||||||
| chr7:148743012 | C | T | 11 | a0001c0001t0001g0092 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.141-10964C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743012 | |||||||
| chr7:148743098 | T | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(9): Show |
12 | HG00738.hp2 HG01175.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.141-10878T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743098 | |||||||
| chr7:148743196 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.141-10780C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743196 | |||||||
| chr7:148743197 | T | G | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.141-10779T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743197 | |||||||
| chr7:148743243 | C | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.141-10733C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743243 | |||||||
| chr7:148743484 | A | G | 15 | a0001c0001t0001g0092 a0001c0001t0001g0110 a0001c0001t0001g0111 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.141-10492A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743484 | |||||||
| chr7:148743544 | A | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(6): Show |
9 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-10432A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743544 | |||||||
| chr7:148743548 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.141-10428A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743548 | |||||||
| chr7:148743620 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.141-10356T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743620 | |||||||
| chr7:148743650 | T | C | 103 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
103 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.141-10326T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743650 | |||||||
| chr7:148743662 | GGGAGGCC others(17): Show |
G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0272 |
3 | HG01346.hp1 HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.141-10289_141-1026 others(28): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148743662 | ||||||
| chr7:148743687 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.141-10289G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743687 | |||||||
| chr7:148743723 | T | C | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
88 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.141-10253T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743723 | |||||||
| chr7:148743773 | C | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.141-10203C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743773 | |||||||
| chr7:148743794 | G | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(9): Show |
12 | HG00738.hp2 HG01175.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.141-10182G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743794 | |||||||
| chr7:148743877 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.141-10099G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743877 | |||||||
| chr7:148743897 | A | G | 9 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-10079A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743897 | |||||||
| chr7:148743900 | T | C | 9 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-10076T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148743900 | |||||||
| chr7:148744308 | G | T | 139 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
139 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.141-9668G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744308 | |||||||
| chr7:148744397 | A | AGT | 22 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0117 others(19): Show |
22 | HG01168.hp2 HG02135.hp2 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.141-9539_141-9538d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744397 | A | AGTGT | 6 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0139 others(3): Show |
6 | HG01433.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-9541_141-9538d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744397 | A | AGTGTGT | 3 | a0001c0001t0001g0168 a0001c0001t0001g0201 a0001c0001t0001g0253 |
3 | HG02055.hp2 HG02145.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.141-9543_141-9538d others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744397 | AGT | A | 41 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0037 others(38): Show |
41 | HG00673.hp1 HG00738.hp2 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.141-9539_141-9538d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744397 | AGTGT | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(46): Show |
49 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.141-9541_141-9538d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744397 | AGTGTGT | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(37): Show |
40 | HG00438.hp2 HG00639.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.141-9543_141-9538d others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744397 | AGTGTGTG others(1): Show |
A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0083 a0001c0001t0001g0304 others(1): Show |
4 | HG02155.hp1 HG02451.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-9545_141-9538d others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744397 | AGTGTGTG others(5): Show |
A | 9 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-9549_141-9538d others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744397 | AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.141-9551_141-9538d others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744397 | AGTGTGTG others(9): Show |
A | 2 | a0001c0002t0001g0255 a0001c0005t0001g0256 |
2 | HG00408.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.141-9553_141-9538d others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744397 | AGTGTGTG others(11): Show |
A | 66 | a0001c0001t0001g0067 a0001c0001t0001g0091 a0001c0001t0001g0132 others(63): Show |
66 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.141-9555_141-9538d others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148744397 | ||||||
| chr7:148744574 | G | T | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.141-9402G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744574 | |||||||
| chr7:148744599 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.141-9377T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744599 | |||||||
| chr7:148744666 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.141-9310A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744666 | |||||||
| chr7:148744682 | A | T | 2 | a0001c0003t0001g0108 a0001c0003t0001g0109 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.141-9294A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744682 | |||||||
| chr7:148744979 | T | G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(6): Show |
9 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-8997T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148744979 | |||||||
| chr7:148745008 | T | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(9): Show |
12 | HG00738.hp2 HG01175.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.141-8968T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745008 | |||||||
| chr7:148745119 | G | A | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.141-8857G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745119 | |||||||
| chr7:148745200 | G | C | 11 | a0001c0001t0001g0092 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.141-8776G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745200 | |||||||
| chr7:148745359 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.141-8617G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745359 | |||||||
| chr7:148745573 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.141-8403C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745573 | |||||||
| chr7:148745655 | A | G | 17 | a0001c0001t0001g0067 a0001c0001t0001g0265 a0001c0001t0001g0290 others(14): Show |
17 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.141-8321A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745655 | |||||||
| chr7:148745679 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.141-8297A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745679 | |||||||
| chr7:148745883 | C | T | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-8093C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148745883 | |||||||
| chr7:148746040 | G | A | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-7936G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746040 | |||||||
| chr7:148746064 | A | G | 17 | a0001c0001t0001g0092 a0001c0001t0001g0110 a0001c0001t0001g0111 others(14): Show |
17 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.141-7912A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746064 | |||||||
| chr7:148746117 | T | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0092 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-7859T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746117 | |||||||
| chr7:148746369 | C | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
103 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.141-7607C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746369 | |||||||
| chr7:148746373 | C | CA | 10 | a0001c0001t0001g0119 a0001c0001t0001g0135 a0001c0001t0001g0136 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-7602dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148746373 | ||||||
| chr7:148746471 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.141-7505C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746471 | |||||||
| chr7:148746968 | C | G | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.141-7008C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148746968 | |||||||
| chr7:148747016 | T | C | 22 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0102 others(19): Show |
22 | HG00738.hp2 HG01175.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.141-6960T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747016 | |||||||
| chr7:148747089 | A | G | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | HG00140.hp2 HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.141-6887A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747089 | |||||||
| chr7:148747114 | C | T | 11 | a0001c0001t0001g0092 a0001c0001t0001g0119 a0001c0001t0001g0135 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.141-6862C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747114 | |||||||
| chr7:148747263 | C | A | 21 | a0001c0001t0001g0083 a0001c0001t0001g0102 a0001c0001t0001g0103 others(18): Show |
21 | HG00738.hp2 HG01175.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.141-6713C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747263 | |||||||
| chr7:148747344 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.141-6632T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747344 | |||||||
| chr7:148747632 | G | A | 32 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
32 | HG00738.hp2 HG01175.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.141-6344G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747632 | |||||||
| chr7:148747753 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.141-6223A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747753 | |||||||
| chr7:148747786 | C | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
152 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.141-6190C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747786 | |||||||
| chr7:148747809 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.141-6167G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747809 | |||||||
| chr7:148747875 | GATCATTG others(143): Show |
G | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-6098_141-5949d others(2): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148747875 | ||||||
| chr7:148747981 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.141-5995A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148747981 | |||||||
| chr7:148748200 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.141-5776C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748200 | |||||||
| chr7:148748377 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0128 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.141-5599G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748377 | |||||||
| chr7:148748415 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.141-5561G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748415 | |||||||
| chr7:148748561 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.141-5415C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748561 | |||||||
| chr7:148748606 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.141-5370A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748606 | |||||||
| chr7:148748716 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(215): Show |
220 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.141-5260T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148748716 | |||||||
| chr7:148749081 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
212 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.141-4895G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749081 | |||||||
| chr7:148749207 | A | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0291 |
2 | NA19004.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.141-4769A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749207 | |||||||
| chr7:148749245 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.141-4731C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749245 | |||||||
| chr7:148749262 | C | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.141-4714C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749262 | |||||||
| chr7:148749285 | T | A | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
104 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.141-4691T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749285 | |||||||
| chr7:148749372 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
82 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.141-4604T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749372 | |||||||
| chr7:148749415 | C | CA | 30 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0034 others(27): Show |
32 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.141-4541dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148749415 | ||||||
| chr7:148749415 | C | CAA | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(7): Show |
10 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-4542_141-4541d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148749415 | ||||||
| chr7:148749415 | C | CAAA | 102 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(99): Show |
102 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.141-4543_141-4541d others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148749415 | ||||||
| chr7:148749415 | C | CAAAA | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): Show |
71 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.141-4544_141-4541d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148749415 | ||||||
| chr7:148749415 | C | CAAAAA | 14 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0039 others(11): Show |
14 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.141-4545_141-4541d others(7): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148749415 | ||||||
| chr7:148749556 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.141-4420C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749556 | |||||||
| chr7:148749557 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.141-4419G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749557 | |||||||
| chr7:148749557 | G | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-4419G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749557 | |||||||
| chr7:148749605 | T | A | 1 | a0001c0001t0001g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.141-4371T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749605 | |||||||
| chr7:148749819 | A | G | 108 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(105): Show |
108 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.141-4157A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749819 | |||||||
| chr7:148749985 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.141-3991A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148749985 | |||||||
| chr7:148750264 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.141-3712C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750264 | |||||||
| chr7:148750294 | C | CT | 113 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
113 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.141-3666dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148750294 | ||||||
| chr7:148750294 | C | CTT | 6 | a0001c0001t0001g0071 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG01978.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-3667_141-3666d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148750294 | ||||||
| chr7:148750294 | CT | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0034 others(21): Show |
26 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.141-3666delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148750294 | ||||||
| chr7:148750311 | A | T | 1 | a0001c0001t0001g0263 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.141-3665A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750311 | |||||||
| chr7:148750396 | C | A | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-3580C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750396 | |||||||
| chr7:148750473 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.141-3503T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750473 | |||||||
| chr7:148750658 | C | T | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
104 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.141-3318C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750658 | |||||||
| chr7:148750682 | C | G | 10 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0165 others(7): Show |
10 | HG00280.hp1 HG00735.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-3294C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750682 | |||||||
| chr7:148750836 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0081 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.141-3140T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750836 | |||||||
| chr7:148750842 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.141-3134G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750842 | |||||||
| chr7:148750894 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.141-3082C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750894 | |||||||
| chr7:148750984 | TA | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
95 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.141-2977delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148750984 | ||||||
| chr7:148750984 | TAA | T | 107 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.141-2978_141-2977d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148750984 | ||||||
| chr7:148750994 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.141-2982A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750994 | |||||||
| chr7:148750995 | A | C | 1 | a0001c0001t0002g0164 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.141-2981A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148750995 | |||||||
| chr7:148751119 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
82 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.141-2857G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751119 | |||||||
| chr7:148751129 | A | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.141-2847A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751129 | |||||||
| chr7:148751161 | C | A | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-2815C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751161 | |||||||
| chr7:148751353 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.141-2623A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751353 | |||||||
| chr7:148751420 | C | G | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-2556C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751420 | |||||||
| chr7:148751421 | G | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-2555G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751421 | |||||||
| chr7:148751422 | C | G | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-2554C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751422 | |||||||
| chr7:148751459 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0187 |
2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.141-2517C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751459 | |||||||
| chr7:148751534 | C | CA | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0016 others(97): Show |
100 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.141-2422dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148751534 | ||||||
| chr7:148751534 | C | CAA | 11 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0141 others(8): Show |
11 | HG00423.hp2 HG00642.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.141-2423_141-2422d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148751534 | ||||||
| chr7:148751534 | CA | C | 6 | a0001c0001t0001g0066 a0001c0001t0001g0150 a0001c0001t0001g0152 others(3): Show |
6 | HG03209.hp1 NA18941.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-2422delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148751534 | ||||||
| chr7:148751551 | A | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
80 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.141-2425A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751551 | |||||||
| chr7:148751563 | G | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.141-2413G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751563 | |||||||
| chr7:148751584 | T | G | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.141-2392T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751584 | |||||||
| chr7:148751832 | T | C | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
104 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.141-2144T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148751832 | |||||||
| chr7:148752006 | C | G | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.141-1970C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752006 | |||||||
| chr7:148752071 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.141-1905A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752071 | |||||||
| chr7:148752311 | G | A | 77 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0091 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.141-1665G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752311 | |||||||
| chr7:148752373 | G | A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.141-1603G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752373 | |||||||
| chr7:148752384 | AGTT | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(25): Show |
28 | HG00738.hp2 HG01175.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.141-1588_141-1586d others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148752384 | ||||||
| chr7:148752471 | C | A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.141-1505C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752471 | |||||||
| chr7:148752477 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.141-1499T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752477 | |||||||
| chr7:148752572 | A | AT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.141-1397dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148752572 | ||||||
| chr7:148752749 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.141-1227T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148752749 | |||||||
| chr7:148753158 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.141-818C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753158 | |||||||
| chr7:148753159 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0205 a0001c0001t0001g0285 |
3 | NA18968.hp1 NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.141-817G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753159 | |||||||
| chr7:148753255 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.141-721G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753255 | |||||||
| chr7:148753429 | C | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
197 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.141-547C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753429 | |||||||
| chr7:148753477 | G | GAT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
83 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.141-498_141-497dup others(2): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr7 | 148753477 | ||||||
| chr7:148753807 | C | G | 1 | a0001c0001t0002g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.141-169C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753807 | |||||||
| chr7:148753914 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.141-62T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 2/21 | chr7 | 148753914 | |||||||
| chr7:148754264 | C | T | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+114C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754264 | |||||||
| chr7:148754424 | C | T | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.315+274C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754424 | |||||||
| chr7:148754465 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.315+315G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754465 | |||||||
| chr7:148754504 | G | A | 2 | a0001c0003t0001g0108 a0001c0003t0001g0109 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.315+354G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754504 | |||||||
| chr7:148754624 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.315+474G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754624 | |||||||
| chr7:148754797 | A | C | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+647A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754797 | |||||||
| chr7:148754858 | C | T | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+708C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754858 | |||||||
| chr7:148754859 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0207 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.315+709G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754859 | |||||||
| chr7:148754900 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+750C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754900 | |||||||
| chr7:148754902 | A | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+752A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754902 | |||||||
| chr7:148754904 | A | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+754A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148754904 | |||||||
| chr7:148755018 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0003g0166 |
2 | HG01074.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.315+868G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755018 | |||||||
| chr7:148755280 | T | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+1130T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755280 | |||||||
| chr7:148755281 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+1131C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755281 | |||||||
| chr7:148755282 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+1132C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755282 | |||||||
| chr7:148755283 | T | C | 1 | a0001c0001t0001g0028 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.315+1133T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755283 | |||||||
| chr7:148755330 | C | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
197 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.315+1180C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755330 | |||||||
| chr7:148755557 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0071 others(4): Show |
7 | HG01433.hp2 HG01952.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.315+1407G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755557 | |||||||
| chr7:148755662 | A | T | 6 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0140 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-1321A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755662 | |||||||
| chr7:148755813 | C | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.316-1170C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755813 | |||||||
| chr7:148755939 | C | G | 3 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0244 |
3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.316-1044C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148755939 | |||||||
| chr7:148756359 | G | A | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.316-624G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756359 | |||||||
| chr7:148756367 | G | A | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.316-616G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756367 | |||||||
| chr7:148756421 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.316-562C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756421 | |||||||
| chr7:148756520 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.316-463A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756520 | |||||||
| chr7:148756595 | C | G | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.316-388C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756595 | |||||||
| chr7:148756784 | T | A | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-199T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756784 | |||||||
| chr7:148756904 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01433.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.316-79G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 3/21 | chr7 | 148756904 | |||||||
| chr7:148757676 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
196 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.483+526T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757676 | |||||||
| chr7:148757851 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.483+701T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757851 | |||||||
| chr7:148757879 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.483+729A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757879 | |||||||
| chr7:148757896 | C | G | 21 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0265 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.483+746C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757896 | |||||||
| chr7:148757906 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.483+756G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757906 | |||||||
| chr7:148757948 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0212 |
2 | HG01168.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.483+798C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148757948 | |||||||
| chr7:148758021 | G | T | 2 | a0001c0001t0002g0162 a0001c0001t0002g0207 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.483+871G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148758021 | |||||||
| chr7:148758022 | T | C | 2 | a0001c0001t0002g0162 a0001c0001t0002g0207 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.483+872T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148758022 | |||||||
| chr7:148758330 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.484-974G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148758330 | |||||||
| chr7:148758618 | A | G | 3 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0244 |
3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.484-686A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148758618 | |||||||
| chr7:148759034 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.484-270C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148759034 | |||||||
| chr7:148759062 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
250 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.484-242C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148759062 | |||||||
| chr7:148759082 | T | G | 3 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0244 |
3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.484-222T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148759082 | |||||||
| chr7:148759110 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.484-194G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148759110 | |||||||
| chr7:148759233 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.484-71T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 4/21 | chr7 | 148759233 | |||||||
| chr7:148760572 | A | G | 3 | a0001c0001t0001g0091 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG00741.hp2 HG01978.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.789+76A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760572 | |||||||
| chr7:148760683 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.789+187C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760683 | |||||||
| chr7:148760706 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.789+210G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760706 | |||||||
| chr7:148760751 | G | C | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.789+255G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760751 | |||||||
| chr7:148760823 | A | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.789+327A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760823 | |||||||
| chr7:148760834 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.789+338T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760834 | |||||||
| chr7:148760913 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.789+417G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148760913 | |||||||
| chr7:148761049 | C | T | 3 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0244 |
3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.789+553C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761049 | |||||||
| chr7:148761092 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0022 |
3 | HG02056.hp1 NA18954.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.789+596C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761092 | |||||||
| chr7:148761382 | G | A | 6 | a0001c0001t0001g0119 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG01257.hp2 HG01261.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.789+886G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761382 | |||||||
| chr7:148761426 | G | C | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.789+930G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761426 | |||||||
| chr7:148761435 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0167 |
2 | HG01074.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.789+939T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761435 | |||||||
| chr7:148761531 | T | A | 17 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0275 others(14): Show |
17 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.789+1035T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761531 | |||||||
| chr7:148761552 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(135): Show |
140 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.789+1056C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761552 | |||||||
| chr7:148761715 | C | T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG00597.hp2 NA18966.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.789+1219C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761715 | |||||||
| chr7:148761716 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.789+1220G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761716 | |||||||
| chr7:148761879 | G | A | 6 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0140 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.789+1383G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761879 | |||||||
| chr7:148761996 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.789+1500G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148761996 | |||||||
| chr7:148762557 | C | T | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.789+2061C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762557 | |||||||
| chr7:148762583 | T | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0034 others(20): Show |
25 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.789+2087T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762583 | |||||||
| chr7:148762594 | A | G | 7 | a0001c0001t0001g0083 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
7 | HG01884.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.789+2098A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762594 | |||||||
| chr7:148762880 | C | T | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+2384C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762880 | |||||||
| chr7:148762934 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.789+2438G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762934 | |||||||
| chr7:148762937 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.789+2441G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148762937 | |||||||
| chr7:148763017 | G | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG01257.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.789+2521G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763017 | |||||||
| chr7:148763020 | G | A | 2 | a0001c0002t0001g0271 a0001c0002t0001g0306 |
2 | NA18955.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.789+2524G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763020 | |||||||
| chr7:148763022 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.789+2526C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763022 | |||||||
| chr7:148763152 | A | T | 10 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+2656A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763152 | |||||||
| chr7:148763158 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.789+2662T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763158 | |||||||
| chr7:148763180 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02109.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.789+2684C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763180 | |||||||
| chr7:148763183 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.789+2687G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763183 | |||||||
| chr7:148763218 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.789+2722T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763218 | |||||||
| chr7:148763397 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.789+2901C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763397 | |||||||
| chr7:148763424 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.789+2928A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763424 | |||||||
| chr7:148763444 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0034 others(21): Show |
26 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.789+2948T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763444 | |||||||
| chr7:148763500 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.789+3004A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763500 | |||||||
| chr7:148763751 | A | G | 1 | a0001c0001t0004g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.790-2810A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763751 | |||||||
| chr7:148763757 | T | G | 1 | a0001c0001t0001g0268 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.790-2804T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763757 | |||||||
| chr7:148763862 | A | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.790-2699A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763862 | |||||||
| chr7:148763910 | C | T | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.790-2651C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148763910 | |||||||
| chr7:148764010 | GT | G | 12 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(9): Show |
12 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.790-2548delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr7 | 148764010 | ||||||
| chr7:148764058 | A | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.790-2503A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764058 | |||||||
| chr7:148764327 | T | G | 1 | a0001c0001t0001g0326 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.790-2234T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764327 | |||||||
| chr7:148764504 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.790-2057G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764504 | |||||||
| chr7:148764753 | T | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.790-1808T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764753 | |||||||
| chr7:148764977 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.790-1584C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764977 | |||||||
| chr7:148764990 | T | G | 1 | a0001c0001t0001g0294 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.790-1571T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148764990 | |||||||
| chr7:148765058 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0071 others(13): Show |
16 | HG01433.hp2 HG01952.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.790-1503G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765058 | |||||||
| chr7:148765085 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0029 others(3): Show |
6 | HG00741.hp1 HG01081.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.790-1476A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765085 | |||||||
| chr7:148765268 | C | A | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.790-1293C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765268 | |||||||
| chr7:148765309 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.790-1252C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765309 | |||||||
| chr7:148765401 | A | G | 80 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0094 others(77): Show |
80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.790-1160A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765401 | |||||||
| chr7:148765519 | G | A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.790-1042G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765519 | |||||||
| chr7:148765628 | T | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | NA18951.hp1 NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.790-933T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765628 | |||||||
| chr7:148765726 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.790-835A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765726 | |||||||
| chr7:148765766 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.790-795T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765766 | |||||||
| chr7:148765999 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(135): Show |
140 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.790-562T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148765999 | |||||||
| chr7:148766049 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.790-512C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148766049 | |||||||
| chr7:148766088 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.790-473A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148766088 | |||||||
| chr7:148766206 | C | CTA | 75 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0094 others(72): Show |
75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.790-353_790-352dup others(2): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr7 | 148766206 | ||||||
| chr7:148766375 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0070 others(93): Show |
97 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.790-186T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 7/21 | chr7 | 148766375 | |||||||
| chr7:148766768 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(255): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.952+45T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | chr7 | 148766768 | |||||||
| chr7:148766845 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.952+122T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | chr7 | 148766845 | |||||||
| chr7:148766967 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.952+244C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | chr7 | 148766967 | |||||||
| chr7:148767328 | A | AT | 47 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0086 others(44): Show |
47 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.953-279dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr7 | 148767328 | ||||||
| chr7:148767374 | G | A | 13 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(10): Show |
13 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.953-245G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | chr7 | 148767374 | |||||||
| chr7:148767583 | T | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(255): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.953-36T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 8/21 | chr7 | 148767583 | |||||||
| chr7:148767942 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | NA19072.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1083+193C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148767942 | |||||||
| chr7:148767945 | C | T | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+196C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148767945 | |||||||
| chr7:148767957 | G | C | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+208G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148767957 | |||||||
| chr7:148768051 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1083+302G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768051 | |||||||
| chr7:148768067 | A | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0170 others(1): Show |
4 | HG00280.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+318A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768067 | |||||||
| chr7:148768067 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1083+318A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768067 | |||||||
| chr7:148768105 | A | G | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1083+356A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768105 | |||||||
| chr7:148768378 | C | CTTTTTTT | 7 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0119 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083+647_1083+653d others(9): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | ||||||
| chr7:148768378 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1083+641_1083+653d others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | ||||||
| chr7:148768378 | CT | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
65 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1083+653delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | ||||||
| chr7:148768378 | CTTTT | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(156): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1083+650_1083+653d others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | ||||||
| chr7:148768378 | CTTTTT | C | 67 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0017 others(64): Show |
67 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1083+649_1083+653d others(7): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | ||||||
| chr7:148768378 | CTTTTTT | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0110 a0001c0001t0001g0237 others(9): Show |
12 | HG00738.hp2 HG01175.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+648_1083+653d others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148768378 | ||||||
| chr7:148768628 | G | A | 9 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(6): Show |
9 | HG02647.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1083+879G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768628 | |||||||
| chr7:148768632 | G | A | 12 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(9): Show |
12 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+883G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768632 | |||||||
| chr7:148768676 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0081 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1083+927C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768676 | |||||||
| chr7:148768719 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1083+970C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768719 | |||||||
| chr7:148768777 | G | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0029 others(3): Show |
6 | HG00741.hp1 HG01081.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+1028G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768777 | |||||||
| chr7:148768881 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1083+1132C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768881 | |||||||
| chr7:148768896 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.1083+1147T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768896 | |||||||
| chr7:148768976 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1083+1227C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148768976 | |||||||
| chr7:148769026 | G | C | 24 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
24 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1083+1277G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769026 | |||||||
| chr7:148769027 | A | T | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+1278A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769027 | |||||||
| chr7:148769033 | C | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+1284C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769033 | |||||||
| chr7:148769101 | G | A | 12 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(9): Show |
12 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+1352G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769101 | |||||||
| chr7:148769151 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1083+1402G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769151 | |||||||
| chr7:148769192 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1083+1443T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769192 | |||||||
| chr7:148769199 | G | A | 17 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(14): Show |
17 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1083+1450G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769199 | |||||||
| chr7:148769371 | C | T | 1 | a0001c0005t0001g0256 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1083+1622C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769371 | |||||||
| chr7:148769397 | T | TCA | 30 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0033 others(27): Show |
30 | HG00558.hp2 HG01258.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1083+1699_1083+170 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | T | TCACA | 37 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(34): Show |
38 | HG00423.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1083+1697_1083+170 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | T | TCACACA | 12 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0027 others(9): Show |
12 | HG00609.hp1 HG01358.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.1083+1695_1083+170 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | T | TCACACAC others(1): Show |
22 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0037 others(19): Show |
22 | HG00621.hp2 HG01433.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1083+1693_1083+170 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | T | TCACACAC others(3): Show |
3 | a0001c0001t0001g0025 a0001c0001t0001g0311 a0001c0001t0002g0206 |
3 | HG02896.hp2 NA18906.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1083+1691_1083+170 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | T | TCACACAC others(5): Show |
1 | a0001c0001t0001g0204 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1083+1689_1083+170 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | T | TCACACAC others(7): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0047 others(2): Show |
5 | HG02258.hp2 HG02647.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1083+1687_1083+170 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | T | TCACACAC others(9): Show |
1 | a0001c0001t0001g0048 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1083+1685_1083+170 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | T | TCACACAC others(11): Show |
1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1083+1683_1083+170 others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | TCA | T | 47 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0023 others(44): Show |
47 | HG00597.hp2 HG00621.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.1083+1699_1083+170 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | TCACA | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(43): Show |
48 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1083+1697_1083+170 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | TCACACA | T | 18 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0170 others(15): Show |
18 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.1083+1695_1083+170 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | TCACACAC others(1): Show |
T | 34 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0092 others(31): Show |
34 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1083+1693_1083+170 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | TCACACAC others(3): Show |
T | 7 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(4): Show |
7 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083+1691_1083+170 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | TCACACAC others(5): Show |
T | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1083+1689_1083+170 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | TCACACAC others(9): Show |
T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0330 |
3 | NA18971.hp1 NA18986.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1083+1685_1083+170 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769397 | TCACACAC others(11): Show |
T | 1 | a0001c0001t0001g0308 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1083+1683_1083+170 others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769397 | ||||||
| chr7:148769444 | CACACA | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0165 a0001c0001t0001g0267 others(1): Show |
4 | HG00408.hp2 HG02055.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+1697_1083+170 others(9): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148769444 | ||||||
| chr7:148769450 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1083+1701A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769450 | |||||||
| chr7:148769458 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1083+1709A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769458 | |||||||
| chr7:148769787 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1083+2038C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769787 | |||||||
| chr7:148769931 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1083+2182C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148769931 | |||||||
| chr7:148770355 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0034 others(21): Show |
26 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.1083+2606T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770355 | |||||||
| chr7:148770373 | A | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+2624A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770373 | |||||||
| chr7:148770510 | C | G | 1 | a0001c0001t0001g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1083+2761C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770510 | |||||||
| chr7:148770582 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1083+2833C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770582 | |||||||
| chr7:148770585 | T | C | 17 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(14): Show |
17 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1083+2836T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770585 | |||||||
| chr7:148770631 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1083+2882C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770631 | |||||||
| chr7:148770632 | G | A | 12 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(9): Show |
12 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+2883G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770632 | |||||||
| chr7:148770673 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1083+2924C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770673 | |||||||
| chr7:148770726 | C | T | 3 | a0001c0001t0001g0185 a0001c0001t0001g0219 a0001c0001t0001g0221 |
3 | HG00597.hp2 HG00639.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1083+2977C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770726 | |||||||
| chr7:148770818 | A | C | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1083+3069A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770818 | |||||||
| chr7:148770936 | C | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(254): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1083+3187C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148770936 | |||||||
| chr7:148771031 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0207 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1083+3282G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771031 | |||||||
| chr7:148771352 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1083+3603A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771352 | |||||||
| chr7:148771353 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1083+3604C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771353 | |||||||
| chr7:148771357 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1083+3608T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771357 | |||||||
| chr7:148771429 | T | C | 1 | a0001c0001t0001g0324 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1083+3680T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771429 | |||||||
| chr7:148771525 | C | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(129): Show |
134 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.1083+3776C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771525 | |||||||
| chr7:148771554 | G | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0175 a0001c0001t0001g0181 others(1): Show |
4 | NA18955.hp1 NA18984.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+3805G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771554 | |||||||
| chr7:148771830 | A | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+4081A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771830 | |||||||
| chr7:148771943 | C | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | NA18975.hp1 NA19065.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1083+4194C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148771943 | |||||||
| chr7:148772093 | A | G | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1083+4344A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772093 | |||||||
| chr7:148772136 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1083+4387C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772136 | |||||||
| chr7:148772140 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1083+4391C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772140 | |||||||
| chr7:148772278 | G | A | 1 | a0001c0001t0001g0330 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1083+4529G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772278 | |||||||
| chr7:148772289 | C | T | 12 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(9): Show |
12 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1083+4540C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772289 | |||||||
| chr7:148772347 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1083+4598G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772347 | |||||||
| chr7:148772420 | A | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(221): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1083+4671A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772420 | |||||||
| chr7:148772425 | C | CA | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(238): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1083+4687dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148772425 | ||||||
| chr7:148772425 | C | CAA | 12 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(9): Show |
12 | HG02155.hp2 HG02257.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1083+4686_1083+468 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148772425 | ||||||
| chr7:148772429 | A | AC | 3 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0121 |
3 | HG02109.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1083+4680_1083+468 others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772429 | |||||||
| chr7:148772515 | A | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+4766A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772515 | |||||||
| chr7:148772624 | C | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(254): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1083+4875C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772624 | |||||||
| chr7:148772737 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1083+4988G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772737 | |||||||
| chr7:148772743 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1083+4994A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772743 | |||||||
| chr7:148772828 | G | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+5079G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772828 | |||||||
| chr7:148772905 | C | T | 9 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(6): Show |
9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1083+5156C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148772905 | |||||||
| chr7:148773068 | C | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(217): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1083+5319C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773068 | |||||||
| chr7:148773227 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(135): Show |
140 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.1083+5478C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773227 | |||||||
| chr7:148773268 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0321 others(2): Show |
6 | HG00280.hp2 HG01071.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+5519A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773268 | |||||||
| chr7:148773321 | T | C | 3 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0244 |
3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1083+5572T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773321 | |||||||
| chr7:148773383 | C | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG02257.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1083+5634C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773383 | |||||||
| chr7:148773406 | A | G | 106 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(103): Show |
106 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1083+5657A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773406 | |||||||
| chr7:148773547 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1083+5798C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773547 | |||||||
| chr7:148773626 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1083+5877G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773626 | |||||||
| chr7:148773657 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0118 a0001c0001t0001g0131 others(1): Show |
4 | HG01952.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+5908G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773657 | |||||||
| chr7:148773901 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1083+6152C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773901 | |||||||
| chr7:148773957 | T | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0257 |
2 | HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1083+6208T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148773957 | |||||||
| chr7:148774069 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1083+6320G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774069 | |||||||
| chr7:148774143 | C | T | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+6394C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774143 | |||||||
| chr7:148774145 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1083+6396T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774145 | |||||||
| chr7:148774237 | A | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG02257.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1083+6488A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774237 | |||||||
| chr7:148774492 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1083+6743C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774492 | |||||||
| chr7:148774551 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1083+6802A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774551 | |||||||
| chr7:148774639 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1083+6890A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774639 | |||||||
| chr7:148774669 | G | A | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0122 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+6920G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774669 | |||||||
| chr7:148774713 | A | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+6964A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774713 | |||||||
| chr7:148774746 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG03017.hp1 HG03490.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1083+6997C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774746 | |||||||
| chr7:148774747 | T | G | 3 | a0001c0003t0001g0122 a0001c0003t0001g0129 a0001c0003t0001g0309 |
3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1083+6998T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774747 | |||||||
| chr7:148774998 | A | G | 4 | a0001c0001t0001g0260 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG02647.hp2 HG03209.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+7249A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148774998 | |||||||
| chr7:148775461 | T | C | 24 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
24 | HG00558.hp1 HG00558.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1083+7712T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148775461 | |||||||
| chr7:148775766 | C | T | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1083+8017C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148775766 | |||||||
| chr7:148775811 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1084-7972T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148775811 | |||||||
| chr7:148775855 | G | GA | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(125): Show |
130 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.1084-7913dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148775855 | ||||||
| chr7:148775855 | GA | G | 17 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(14): Show |
17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1084-7913delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148775855 | ||||||
| chr7:148776051 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0068 |
3 | HG00558.hp1 NA18992.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1084-7732G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776051 | |||||||
| chr7:148776092 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1084-7691A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776092 | |||||||
| chr7:148776177 | A | AC | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(225): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1084-7600dupC | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776177 | ||||||
| chr7:148776214 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0184 |
2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1084-7569C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776214 | |||||||
| chr7:148776292 | TCTAACAT others(7): Show |
T | 1 | a0001c0001t0001g0310 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1084-7488_1084-747 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776292 | ||||||
| chr7:148776292 | TCTAACAT others(8): Show |
T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0311 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1084-7490_1084-747 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776292 | |||||||
| chr7:148776293 | C | T | 1 | a0001c0001t0004g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1084-7490C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776293 | |||||||
| chr7:148776294 | TAACATAA others(6): Show |
T | 1 | a0001c0001t0004g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1084-7488_1084-747 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776294 | |||||||
| chr7:148776307 | C | CT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0022 others(18): Show |
21 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1084-7449dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTT | 40 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0039 others(37): Show |
40 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1084-7454_1084-744 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0034 others(46): Show |
50 | HG00140.hp1 HG00642.hp1 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.1084-7455_1084-744 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(1): Show |
26 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0102 others(23): Show |
27 | HG00280.hp2 HG01071.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1084-7456_1084-744 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(2): Show |
19 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0001g0099 others(16): Show |
19 | HG00597.hp2 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1084-7457_1084-744 others(13): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(3): Show |
20 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0070 others(17): Show |
20 | HG00597.hp1 HG01109.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1084-7458_1084-744 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(4): Show |
23 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(20): Show |
23 | HG00280.hp1 HG00408.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1084-7459_1084-744 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0145 a0001c0001t0001g0184 a0001c0001t0001g0229 others(5): Show |
8 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-7460_1084-744 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(6): Show |
5 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0001g0180 others(2): Show |
5 | HG01168.hp2 HG02559.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084-7461_1084-744 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0266 a0001c0001t0001g0312 |
2 | HG02040.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1084-7462_1084-744 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(8): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0188 a0001c0001t0001g0268 others(5): Show |
8 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-7463_1084-744 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(9): Show |
9 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0001g0281 others(6): Show |
9 | HG00140.hp2 HG00642.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-7464_1084-744 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0267 a0001c0001t0001g0291 |
2 | NA19004.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1084-7465_1084-744 others(21): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0277 a0001c0001t0001g0293 |
2 | HG03239.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1084-7467_1084-744 others(23): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0250 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1084-7469_1084-744 others(25): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0165 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1084-7474_1084-744 others(30): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0292 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1084-7449_1084-744 others(33): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1084-7476C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776307 | |||||||
| chr7:148776307 | CTTTTTT | C | 11 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(8): Show |
11 | HG01175.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1084-7454_1084-744 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776307 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1084-7463_1084-744 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148776307 | ||||||
| chr7:148776385 | C | T | 16 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-7398C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776385 | |||||||
| chr7:148776420 | G | A | 84 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0039 others(81): Show |
84 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.1084-7363G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776420 | |||||||
| chr7:148776617 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02109.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1084-7166G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776617 | |||||||
| chr7:148776661 | A | G | 7 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0194 others(4): Show |
7 | HG02040.hp1 HG02523.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1084-7122A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776661 | |||||||
| chr7:148776755 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1084-7028T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776755 | |||||||
| chr7:148776834 | T | A | 1 | a0001c0001t0001g0294 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1084-6949T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776834 | |||||||
| chr7:148776962 | C | T | 16 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-6821C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148776962 | |||||||
| chr7:148777049 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1084-6734A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777049 | |||||||
| chr7:148777067 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1084-6716G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777067 | |||||||
| chr7:148777171 | G | A | 9 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0073 others(6): Show |
9 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-6612G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777171 | |||||||
| chr7:148777174 | G | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(256): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1084-6609G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777174 | |||||||
| chr7:148777194 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1084-6589A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777194 | |||||||
| chr7:148777267 | T | A | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1084-6516T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777267 | |||||||
| chr7:148777377 | G | A | 17 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(14): Show |
17 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1084-6406G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777377 | |||||||
| chr7:148777506 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0100 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1084-6277G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777506 | |||||||
| chr7:148777618 | T | G | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1084-6165T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777618 | |||||||
| chr7:148777654 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(225): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1084-6129A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777654 | |||||||
| chr7:148777660 | C | T | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084-6123C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777660 | |||||||
| chr7:148777744 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0134 |
2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1084-6039T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148777744 | |||||||
| chr7:148778022 | C | T | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1084-5761C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778022 | |||||||
| chr7:148778070 | C | CA | 10 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(7): Show |
10 | HG00558.hp2 HG02300.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-5686dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAA | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-5687_1084-568 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAA | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0118 others(4): Show |
9 | HG01167.hp2 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-5690_1084-568 others(9): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAA | 9 | a0001c0001t0001g0117 a0001c0001t0001g0132 a0001c0001t0001g0146 others(6): Show |
9 | HG01071.hp1 HG01169.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-5691_1084-568 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA | 10 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0099 others(7): Show |
10 | HG01070.hp1 HG01070.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-5692_1084-568 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(1): Show |
23 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0071 others(20): Show |
23 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1084-5693_1084-568 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(2): Show |
28 | a0001c0001t0001g0070 a0001c0001t0001g0083 a0001c0001t0001g0098 others(25): Show |
28 | HG00423.hp2 HG00639.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1084-5694_1084-568 others(13): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(3): Show |
30 | a0001c0001t0001g0034 a0001c0001t0001g0067 a0001c0001t0001g0100 others(27): Show |
30 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1084-5695_1084-568 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(4): Show |
28 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
28 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1084-5696_1084-568 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(5): Show |
8 | a0001c0001t0001g0035 a0001c0001t0001g0090 a0001c0001t0001g0158 others(5): Show |
8 | HG00642.hp1 HG00673.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1084-5697_1084-568 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0003t0001g0108 |
3 | HG03225.hp1 NA18941.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1084-5698_1084-568 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0163 a0001c0001t0001g0230 |
3 | HG02559.hp1 HG03942.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1084-5699_1084-568 others(18): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(8): Show |
9 | a0001c0001t0001g0092 a0001c0001t0001g0156 a0001c0001t0001g0157 others(6): Show |
9 | HG01071.hp2 HG01109.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-5700_1084-568 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | NA18943.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1084-5701_1084-568 others(20): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1084-5702_1084-568 others(21): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(11): Show |
4 | a0001c0001t0001g0095 a0001c0001t0001g0114 a0001c0001t0001g0127 others(1): Show |
4 | HG01123.hp2 HG02055.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-5703_1084-568 others(22): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0154 a0001c0001t0001g0314 |
2 | HG01993.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1084-5704_1084-568 others(23): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(13): Show |
4 | a0001c0001t0001g0153 a0001c0001t0001g0238 a0001c0001t0002g0162 others(1): Show |
4 | HG01884.hp2 NA18953.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-5705_1084-568 others(24): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0089 a0001c0001t0001g0247 |
2 | NA18984.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1084-5706_1084-568 others(25): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0147 a0001c0004t0001g0211 |
2 | HG02135.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1084-5707_1084-568 others(26): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1084-5708_1084-568 others(27): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084-5709_1084-568 others(28): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(18): Show |
3 | a0001c0001t0001g0120 a0001c0001t0001g0128 a0001c0001t0001g0175 |
3 | HG01243.hp2 NA19011.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1084-5710_1084-568 others(29): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0272 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1084-5686_1084-568 others(35): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778070 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0335 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1084-5686_1084-568 others(36): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778070 | ||||||
| chr7:148778083 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0148 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1084-5697_1084-568 others(19): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778083 | ||||||
| chr7:148778085 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1084-5695_1084-568 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778085 | ||||||
| chr7:148778088 | AAAAAAAA others(3): Show |
A | 16 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(13): Show |
16 | HG01952.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-5692_1084-568 others(14): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778088 | ||||||
| chr7:148778094 | AAAAG | A | 10 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG02080.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-5686_1084-568 others(8): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148778094 | ||||||
| chr7:148778095 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1084-5688A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778095 | |||||||
| chr7:148778097 | AG | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG02647.hp2 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-5685delG | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778097 | |||||||
| chr7:148778098 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(181): Show |
186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1084-5685G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778098 | |||||||
| chr7:148778101 | G | A | 1 | a0001c0004t0001g0211 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1084-5682G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778101 | |||||||
| chr7:148778103 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084-5680A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778103 | |||||||
| chr7:148778272 | A | G | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1084-5511A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778272 | |||||||
| chr7:148778349 | G | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG02257.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1084-5434G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778349 | |||||||
| chr7:148778365 | G | A | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-5418G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778365 | |||||||
| chr7:148778436 | A | G | 19 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(16): Show |
19 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1084-5347A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778436 | |||||||
| chr7:148778571 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1084-5212C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778571 | |||||||
| chr7:148778572 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1084-5211G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778572 | |||||||
| chr7:148778745 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1084-5038C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778745 | |||||||
| chr7:148778836 | G | T | 28 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0144 others(25): Show |
28 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1084-4947G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148778836 | |||||||
| chr7:148779024 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1084-4759A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779024 | |||||||
| chr7:148779278 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1084-4505A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779278 | |||||||
| chr7:148779563 | G | C | 1 | a0001c0001t0001g0022 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1084-4220G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779563 | |||||||
| chr7:148779641 | A | G | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-4142A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779641 | |||||||
| chr7:148779669 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1084-4114C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779669 | |||||||
| chr7:148779838 | AGTGGGCT others(27): Show |
A | 1 | a0001c0001t0001g0290 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1084-3938_1084-390 others(38): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148779838 | ||||||
| chr7:148779970 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0081 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1084-3813A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779970 | |||||||
| chr7:148779996 | G | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(236): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1084-3787G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148779996 | |||||||
| chr7:148780079 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1084-3704T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780079 | |||||||
| chr7:148780113 | GTA | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(235): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1084-3658_1084-365 others(6): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148780113 | ||||||
| chr7:148780211 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0029 others(3): Show |
6 | HG00741.hp1 HG01081.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1084-3572A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780211 | |||||||
| chr7:148780388 | T | G | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-3395T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780388 | |||||||
| chr7:148780497 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(131): Show |
136 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.1084-3286G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780497 | |||||||
| chr7:148780663 | G | A | 5 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0296 others(2): Show |
5 | HG00642.hp2 HG01192.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084-3120G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780663 | |||||||
| chr7:148780747 | A | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0026 others(4): Show |
8 | HG00423.hp1 HG00438.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.1084-3036A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148780747 | |||||||
| chr7:148781079 | A | AT | 10 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0022 others(7): Show |
10 | HG01167.hp1 HG02602.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1084-2682dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | ||||||
| chr7:148781079 | A | ATTTTT | 7 | a0001c0001t0001g0011 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
7 | HG00408.hp2 HG01433.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1084-2686_1084-268 others(9): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | ||||||
| chr7:148781079 | A | ATTTTTT | 65 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0072 others(62): Show |
65 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1084-2687_1084-268 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | ||||||
| chr7:148781079 | A | ATTTTTTT | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(104): Show |
109 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1084-2688_1084-268 others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | ||||||
| chr7:148781079 | A | ATTTTTTT others(1): Show |
60 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0049 others(57): Show |
60 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1084-2689_1084-268 others(12): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | ||||||
| chr7:148781079 | A | ATTTTTTT others(2): Show |
14 | a0001c0001t0001g0009 a0001c0001t0001g0044 a0001c0001t0001g0102 others(11): Show |
14 | HG00738.hp1 HG01175.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1084-2690_1084-268 others(13): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | ||||||
| chr7:148781079 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1084-2692_1084-268 others(15): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | ||||||
| chr7:148781079 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1084-2693_1084-268 others(16): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | ||||||
| chr7:148781079 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0004g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1084-2694_1084-268 others(17): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr7 | 148781079 | ||||||
| chr7:148781109 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0034 others(22): Show |
27 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1084-2674T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781109 | |||||||
| chr7:148781117 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1084-2666C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781117 | |||||||
| chr7:148781123 | C | T | 68 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0095 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1084-2660C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781123 | |||||||
| chr7:148781126 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1084-2657G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781126 | |||||||
| chr7:148781173 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG00741.hp2 HG01978.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1084-2610C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781173 | |||||||
| chr7:148781302 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1084-2481A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781302 | |||||||
| chr7:148781408 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1084-2375T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781408 | |||||||
| chr7:148781628 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(256): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1084-2155T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781628 | |||||||
| chr7:148781761 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1084-2022C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781761 | |||||||
| chr7:148781803 | C | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(237): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1084-1980C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781803 | |||||||
| chr7:148781890 | G | A | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1084-1893G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781890 | |||||||
| chr7:148781959 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1084-1824A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781959 | |||||||
| chr7:148781979 | G | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(236): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1084-1804G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148781979 | |||||||
| chr7:148782078 | G | A | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1084-1705G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782078 | |||||||
| chr7:148782107 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1084-1676G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782107 | |||||||
| chr7:148782201 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1084-1582C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782201 | |||||||
| chr7:148782225 | C | G | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084-1558C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782225 | |||||||
| chr7:148782556 | T | A | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(220): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1084-1227T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782556 | |||||||
| chr7:148782556 | T | G | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084-1227T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782556 | |||||||
| chr7:148782591 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1084-1192T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782591 | |||||||
| chr7:148782643 | T | C | 1 | a0001c0001t0001g0026 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1084-1140T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782643 | |||||||
| chr7:148782657 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1084-1126A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782657 | |||||||
| chr7:148782822 | G | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG00558.hp2 NA18943.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1084-961G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782822 | |||||||
| chr7:148782846 | GC | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(221): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1084-936delC | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782846 | |||||||
| chr7:148782879 | C | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG02257.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1084-904C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782879 | |||||||
| chr7:148782884 | A | G | 16 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-899A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148782884 | |||||||
| chr7:148783022 | G | T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(236): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1084-761G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783022 | |||||||
| chr7:148783141 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(234): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1084-642C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783141 | |||||||
| chr7:148783173 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1084-610C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783173 | |||||||
| chr7:148783182 | C | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0330 |
3 | HG02523.hp2 NA18961.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1084-601C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783182 | |||||||
| chr7:148783377 | C | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0251 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-406C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783377 | |||||||
| chr7:148783667 | A | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1084-116A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 9/21 | chr7 | 148783667 | |||||||
| chr7:148783898 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(151): Show |
156 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(153): Show |
splice_region_variant&intron_variant | LOW | c.1191+8C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 10/21 | chr7 | 148783898 | |||||||
| chr7:148783952 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1192-19T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 10/21 | chr7 | 148783952 | |||||||
| chr7:148784167 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1298+90C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784167 | |||||||
| chr7:148784396 | G | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(232): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1298+319G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784396 | |||||||
| chr7:148784547 | T | A | 8 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1298+470T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784547 | |||||||
| chr7:148784559 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1298+482G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784559 | |||||||
| chr7:148784752 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1298+675A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784752 | |||||||
| chr7:148784881 | A | G | 8 | a0001c0001t0001g0048 a0001c0001t0001g0073 a0001c0001t0001g0076 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.1298+804A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784881 | |||||||
| chr7:148784890 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1298+813T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148784890 | |||||||
| chr7:148785053 | G | A | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1298+976G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785053 | |||||||
| chr7:148785111 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1298+1034G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785111 | |||||||
| chr7:148785145 | G | A | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1298+1068G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785145 | |||||||
| chr7:148785220 | C | T | 14 | a0001c0001t0001g0091 a0001c0001t0001g0114 a0001c0001t0001g0115 others(11): Show |
14 | HG00741.hp2 HG01243.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.1298+1143C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785220 | |||||||
| chr7:148785385 | G | C | 10 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(7): Show |
10 | HG01243.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1299-1166G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785385 | |||||||
| chr7:148785517 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0128 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1299-1034C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785517 | |||||||
| chr7:148785523 | A | AT | 20 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0042 others(17): Show |
20 | HG00642.hp1 HG01123.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1299-1008dupT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr7 | 148785523 | ||||||
| chr7:148785523 | AT | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0020 others(5): Show |
8 | HG01074.hp1 HG02523.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299-1008delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr7 | 148785523 | ||||||
| chr7:148785855 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1299-696C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148785855 | |||||||
| chr7:148786152 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG00423.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1299-399G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148786152 | |||||||
| chr7:148786170 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1299-381A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148786170 | |||||||
| chr7:148786320 | G | C | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1299-231G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148786320 | |||||||
| chr7:148786508 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1299-43C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 11/21 | chr7 | 148786508 | |||||||
| chr7:148786661 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1347+62G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 12/21 | chr7 | 148786661 | |||||||
| chr7:148786668 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(230): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1347+69G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 12/21 | chr7 | 148786668 | |||||||
| chr7:148786927 | A | G | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1348-62A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 12/21 | chr7 | 148786927 | |||||||
| chr7:148786974 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1348-15C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 12/21 | chr7 | 148786974 | |||||||
| chr7:148787189 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02109.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1479+69G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787189 | |||||||
| chr7:148787290 | A | C | 1 | a0001c0001t0004g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1479+170A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787290 | |||||||
| chr7:148787394 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1479+274A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787394 | |||||||
| chr7:148787507 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1479+387G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787507 | |||||||
| chr7:148787627 | C | T | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1479+507C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787627 | |||||||
| chr7:148787646 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1479+526T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787646 | |||||||
| chr7:148787798 | C | T | 16 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1479+678C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787798 | |||||||
| chr7:148787805 | C | G | 1 | a0001c0001t0001g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1479+685C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787805 | |||||||
| chr7:148787886 | G | A | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1480-671G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787886 | |||||||
| chr7:148787923 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1480-634G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787923 | |||||||
| chr7:148787951 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1480-606G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787951 | |||||||
| chr7:148787952 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1480-605C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148787952 | |||||||
| chr7:148788001 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1480-556G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788001 | |||||||
| chr7:148788042 | T | C | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | HG00140.hp2 HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1480-515T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788042 | |||||||
| chr7:148788042 | T | G | 1 | a0001c0002t0001g0280 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1480-515T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788042 | |||||||
| chr7:148788245 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1480-312G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788245 | |||||||
| chr7:148788345 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1480-212A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788345 | |||||||
| chr7:148788359 | A | C | 1 | a0001c0001t0001g0246 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1480-198A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788359 | |||||||
| chr7:148788360 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1480-197G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788360 | |||||||
| chr7:148788437 | CTTTGCTA others(2): Show |
C | 3 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0001g0244 |
3 | HG00738.hp2 HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1480-119_1480-111d others(11): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788437 | |||||||
| chr7:148788511 | G | A | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1480-46G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 13/21 | chr7 | 148788511 | |||||||
| chr7:148788825 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1597+151C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148788825 | |||||||
| chr7:148788862 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1597+188C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148788862 | |||||||
| chr7:148788894 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1597+220G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148788894 | |||||||
| chr7:148789050 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1597+376A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148789050 | |||||||
| chr7:148789165 | A | T | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1597+491A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148789165 | |||||||
| chr7:148789330 | G | C | 34 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0001g0160 others(31): Show |
34 | HG00140.hp1 HG00639.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1598-420G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148789330 | |||||||
| chr7:148789357 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0307 |
2 | HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1598-393C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 14/21 | chr7 | 148789357 | |||||||
| chr7:148790023 | C | T | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1674+197C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790023 | |||||||
| chr7:148790038 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1674+212A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790038 | |||||||
| chr7:148790039 | T | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG02630.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1674+213T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790039 | |||||||
| chr7:148790090 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1675-220C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790090 | |||||||
| chr7:148790110 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1675-200A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790110 | |||||||
| chr7:148790237 | G | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1675-73G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790237 | |||||||
| chr7:148790252 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1675-58C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790252 | |||||||
| chr7:148790303 | T | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(220): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
splice_region_variant&intron_variant | LOW | c.1675-7T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 15/21 | chr7 | 148790303 | |||||||
| chr7:148790745 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0003g0166 |
2 | HG01074.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1806+304G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148790745 | |||||||
| chr7:148790909 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1806+468A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148790909 | |||||||
| chr7:148791035 | G | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0127 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1806+594G>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791035 | |||||||
| chr7:148791152 | C | G | 69 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0095 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1806+711C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791152 | |||||||
| chr7:148791207 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | NA19072.hp1 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1806+766A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791207 | |||||||
| chr7:148791415 | C | T | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(231): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1806+974C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791415 | |||||||
| chr7:148791838 | T | C | 79 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0086 others(76): Show |
79 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1807-888T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791838 | |||||||
| chr7:148791872 | C | T | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(231): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1807-854C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791872 | |||||||
| chr7:148791909 | G | A | 3 | a0001c0003t0001g0122 a0001c0003t0001g0129 a0001c0003t0001g0309 |
3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1807-817G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791909 | |||||||
| chr7:148791911 | C | T | 69 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0095 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1807-815C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791911 | |||||||
| chr7:148791992 | G | A | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0098 others(3): Show |
6 | HG01123.hp2 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1807-734G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148791992 | |||||||
| chr7:148792046 | T | C | 2 | a0001c0002t0001g0271 a0001c0002t0001g0306 |
2 | NA18955.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1807-680T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792046 | |||||||
| chr7:148792052 | G | T | 28 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0144 others(25): Show |
28 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1807-674G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792052 | |||||||
| chr7:148792094 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1807-632G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792094 | |||||||
| chr7:148792117 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1807-609C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792117 | |||||||
| chr7:148792185 | CA | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(223): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1807-526delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr7 | 148792185 | ||||||
| chr7:148792301 | G | T | 8 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1807-425G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792301 | |||||||
| chr7:148792678 | A | C | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1807-48A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792678 | |||||||
| chr7:148792682 | A | G | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1807-44A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 16/21 | chr7 | 148792682 | |||||||
| chr7:148793018 | G | A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1899+200G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793018 | |||||||
| chr7:148793135 | G | A | 16 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1899+317G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793135 | |||||||
| chr7:148793173 | T | C | 4 | a0001c0002t0001g0271 a0001c0002t0001g0278 a0001c0002t0001g0280 others(1): Show |
4 | HG00597.hp1 NA18955.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1899+355T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793173 | |||||||
| chr7:148793174 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1899+356G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793174 | |||||||
| chr7:148793218 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1899+400C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793218 | |||||||
| chr7:148793375 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1899+557C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793375 | |||||||
| chr7:148793742 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1899+924A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793742 | |||||||
| chr7:148793791 | A | G | 16 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1899+973A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793791 | |||||||
| chr7:148793821 | C | A | 16 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1899+1003C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793821 | |||||||
| chr7:148793949 | A | T | 1 | a0001c0001t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1899+1131A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793949 | |||||||
| chr7:148793972 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1899+1154T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148793972 | |||||||
| chr7:148794075 | C | A | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1899+1257C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794075 | |||||||
| chr7:148794085 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0069 |
2 | HG01981.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1899+1267G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794085 | |||||||
| chr7:148794115 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1899+1297C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794115 | |||||||
| chr7:148794233 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1899+1415T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794233 | |||||||
| chr7:148794245 | A | G | 5 | a0001c0001t0001g0130 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1899+1427A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794245 | |||||||
| chr7:148794266 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1899+1448T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794266 | |||||||
| chr7:148794496 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1899+1678G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794496 | |||||||
| chr7:148794917 | C | T | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1899+2099C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794917 | |||||||
| chr7:148794980 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1899+2162C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148794980 | |||||||
| chr7:148795082 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1899+2264C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795082 | |||||||
| chr7:148795123 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG02970.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1899+2305G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795123 | |||||||
| chr7:148795202 | A | G | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1899+2384A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795202 | |||||||
| chr7:148795276 | C | T | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1899+2458C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795276 | |||||||
| chr7:148795366 | A | G | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900-2446A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795366 | |||||||
| chr7:148795424 | A | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 |
3 | HG02055.hp1 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1900-2388A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795424 | |||||||
| chr7:148795533 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1900-2279G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795533 | |||||||
| chr7:148795538 | G | A | 15 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(12): Show |
15 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1900-2274G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795538 | |||||||
| chr7:148795595 | T | G | 1 | a0001c0002t0001g0278 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1900-2217T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795595 | |||||||
| chr7:148795622 | T | A | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900-2190T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795622 | |||||||
| chr7:148795713 | T | G | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1900-2099T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795713 | |||||||
| chr7:148795769 | C | CA | 16 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0147 others(13): Show |
16 | HG00735.hp1 HG02135.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1900-2024dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148795769 | ||||||
| chr7:148795769 | C | CAAAAAA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0071 others(3): Show |
6 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1900-2029_1900-202 others(10): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148795769 | ||||||
| chr7:148795769 | CA | C | 9 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0117 others(6): Show |
9 | HG01167.hp1 HG02723.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1900-2024delA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148795769 | ||||||
| chr7:148795799 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1900-2013A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148795799 | |||||||
| chr7:148796018 | T | TTGTGGTA others(14): Show |
20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900-1789_1900-178 others(25): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148796018 | ||||||
| chr7:148796024 | C | T | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900-1788C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796024 | |||||||
| chr7:148796032 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1900-1780A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796032 | |||||||
| chr7:148796199 | A | G | 20 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
20 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1900-1613A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796199 | |||||||
| chr7:148796220 | A | G | 2 | a0001c0003t0001g0108 a0001c0003t0001g0109 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1900-1592A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796220 | |||||||
| chr7:148796290 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1900-1522C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796290 | |||||||
| chr7:148796511 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(256): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1900-1301A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796511 | |||||||
| chr7:148796648 | C | G | 1 | a0001c0001t0004g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1900-1164C>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796648 | |||||||
| chr7:148796801 | A | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG02257.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1900-1011A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796801 | |||||||
| chr7:148796952 | T | C | 70 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0070 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.1900-860T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148796952 | |||||||
| chr7:148797075 | GT | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1900-734delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797075 | ||||||
| chr7:148797116 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1900-696G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797116 | |||||||
| chr7:148797146 | A | T | 1 | a0001c0001t0004g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1900-666A>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797146 | |||||||
| chr7:148797182 | C | A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0004g0126 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1900-630C>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797182 | |||||||
| chr7:148797188 | A | G | 2 | a0001c0003t0001g0108 a0001c0003t0001g0109 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1900-624A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797188 | |||||||
| chr7:148797258 | C | T | 16 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1900-554C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797258 | |||||||
| chr7:148797395 | C | CA | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(131): Show |
136 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.1900-399dupA | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797395 | ||||||
| chr7:148797395 | C | CAA | 104 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1900-400_1900-399d others(4): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797395 | ||||||
| chr7:148797395 | C | CAAA | 18 | a0001c0001t0001g0034 a0001c0001t0001g0080 a0001c0001t0001g0084 others(15): Show |
18 | HG00738.hp2 HG01175.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.1900-401_1900-399d others(5): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797395 | ||||||
| chr7:148797414 | T | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0240 |
2 | HG01167.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1900-398T>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797414 | |||||||
| chr7:148797424 | G | A | 16 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1900-388G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797424 | |||||||
| chr7:148797486 | C | T | 11 | a0001c0001t0001g0035 a0001c0001t0001g0105 a0001c0001t0001g0106 others(8): Show |
11 | HG01361.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1900-326C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797486 | |||||||
| chr7:148797525 | G | A | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1900-287G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797525 | |||||||
| chr7:148797550 | A | G | 2 | a0001c0001t0001g0314 a0001c0001t0001g0317 |
2 | HG01109.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1900-262A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797550 | |||||||
| chr7:148797653 | T | G | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1900-159T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797653 | |||||||
| chr7:148797666 | C | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(225): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1900-146C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | chr7 | 148797666 | |||||||
| chr7:148797702 | AT | A | 69 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0033 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1900-93delT | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797702 | ||||||
| chr7:148797702 | ATT | A | 23 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(20): Show |
23 | HG01123.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1900-94_1900-93del others(2): Show |
CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr7 | 148797702 | ||||||
| chr7:148798048 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2030+29C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 19/21 | chr7 | 148798048 | |||||||
| chr7:148798176 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2030+157C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 19/21 | chr7 | 148798176 | |||||||
| chr7:148798398 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2031-174C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 19/21 | chr7 | 148798398 | |||||||
| chr7:148798434 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2031-138C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 19/21 | chr7 | 148798434 | |||||||
| chr7:148798548 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2031-24C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 19/21 | chr7 | 148798548 | |||||||
| chr7:148798733 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2136+56G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148798733 | |||||||
| chr7:148798740 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2136+63C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148798740 | |||||||
| chr7:148798768 | A | G | 11 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(8): Show |
11 | HG00738.hp2 HG01175.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2136+91A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148798768 | |||||||
| chr7:148798914 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2136+237T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148798914 | |||||||
| chr7:148799184 | G | A | 16 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(13): Show |
16 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2137-91G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148799184 | |||||||
| chr7:148799186 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2137-89C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 20/21 | chr7 | 148799186 | |||||||
| chr7:148799559 | A | C | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2250+171A>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799559 | |||||||
| chr7:148799691 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0071 others(4): Show |
7 | HG01433.hp2 HG01952.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2250+303A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799691 | |||||||
| chr7:148799733 | T | G | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2250+345T>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799733 | |||||||
| chr7:148799824 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0071 others(3): Show |
6 | HG01433.hp2 HG01978.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2250+436G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799824 | |||||||
| chr7:148799833 | C | T | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2250+445C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799833 | |||||||
| chr7:148799867 | T | C | 21 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(18): Show |
21 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2250+479T>C | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148799867 | |||||||
| chr7:148800068 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2251-434C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800068 | |||||||
| chr7:148800069 | A | G | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2251-433A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800069 | |||||||
| chr7:148800137 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2251-365A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800137 | |||||||
| chr7:148800241 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2251-261G>A | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800241 | |||||||
| chr7:148800296 | C | T | 14 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(11): Show |
14 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2251-206C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800296 | |||||||
| chr7:148800359 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2251-143A>G | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800359 | |||||||
| chr7:148800371 | C | T | 14 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0085 others(11): Show |
14 | HG00738.hp2 HG01175.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2251-131C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800371 | |||||||
| chr7:148800397 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2251-105C>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800397 | |||||||
| chr7:148800417 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2251-85G>T | CUL1 | ENSG00000055130.18 | transcript | ENST00000325222.9 | protein_coding | 21/21 | chr7 | 148800417 |