Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8065 |
| ensemblid | ENSG00000166266.14 |
| hgncid | 2556 |
| symbol | CUL5 |
| name | cullin 5 |
| refseq_nuc | NM_003478.6 |
| refseq_prot | NP_003469.2 |
| ensembl_nuc | ENST00000393094.7 |
| ensembl_prot | ENSP00000376808.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 108008898 |
| end | 108107761 |
| strand | + |
| ver | v1.2 |
| region | chr11:108008898-108107761 |
| region5000 | chr11:108003898-108112761 |
| regionname0 | CUL5_chr11_108008898_108107761 |
| regionname5000 | CUL5_chr11_108003898_108112761 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 780 | 311 | 90 | 53 | 120 | 10 | 36 | 100 | CUL5_chr11_108003898_108112761 | CUL5 | MATSN others(775): Show |
chr11 | 108003898 | 108112761 |
| a0002 | 0/0 | 780 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | MATSN others(775): Show |
chr11 | 108003898 | 108112761 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2340 | 190 | 24 | 34 | 104 | 5 | 22 | CUL5_chr11_108003898_108112761 | CUL5 | ATGGC others(2335): Show |
chr11 | 108003898 | 108112761 | ||
| a0001c0002 | 1/0 | 2340 | 108 | 56 | 19 | 13 | 5 | 14 | CUL5_chr11_108003898_108112761 | CUL5 | ATGGC others(2335): Show |
chr11 | 108003898 | 108112761 | ||
| a0001c0003 | 0/0 | 2340 | 4 | 4 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | ATGGC others(2335): Show |
chr11 | 108003898 | 108112761 | ||
| a0001c0004 | 0/0 | 2340 | 3 | 3 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | ATGGC others(2335): Show |
chr11 | 108003898 | 108112761 | ||
| a0001c0005 | 0/0 | 2340 | 2 | 0 | 0 | 2 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | ATGGC others(2335): Show |
chr11 | 108003898 | 108112761 | ||
| a0001c0006 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | ATGGC others(2335): Show |
chr11 | 108003898 | 108112761 | ||
| a0001c0007 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | ATGGC others(2335): Show |
chr11 | 108003898 | 108112761 | ||
| a0001c0009 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | ATGGC others(2335): Show |
chr11 | 108003898 | 108112761 | ||
| a0002c0008 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | ATGGC others(2335): Show |
chr11 | 108003898 | 108112761 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6172 | 160 | 17 | 21 | 98 | 3 | 21 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0002 | 0/0 | 6171 | 7 | 6 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0006 | 0/0 | 6172 | 5 | 0 | 5 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0010 | 0/0 | 6171 | 3 | 0 | 1 | 2 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0014 | 0/0 | 6172 | 3 | 0 | 3 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0015 | 0/0 | 6172 | 3 | 0 | 1 | 0 | 2 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0018 | 0/1 | 6171 | 1 | 0 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0019 | 0/0 | 6172 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0020 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0021 | 0/0 | 6172 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0022 | 0/0 | 6172 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0023 | 0/0 | 6172 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0024 | 0/0 | 6172 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0026 | 0/0 | 6172 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0001t0028 | 0/0 | 6172 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0001 | 0/0 | 6172 | 4 | 3 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0002 | 0/0 | 6171 | 28 | 9 | 9 | 3 | 4 | 3 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0003 | 0/0 | 6173 | 27 | 9 | 4 | 8 | 0 | 6 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6168): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0004 | 1/0 | 6171 | 15 | 13 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0005 | 0/0 | 6173 | 4 | 4 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6168): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0007 | 0/0 | 6171 | 5 | 0 | 2 | 0 | 1 | 2 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0008 | 0/0 | 6171 | 5 | 2 | 1 | 0 | 0 | 2 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0009 | 0/0 | 6171 | 5 | 5 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0010 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0011 | 0/0 | 6172 | 4 | 3 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0013 | 0/0 | 6171 | 3 | 3 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0017 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6180): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0025 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0027 | 0/0 | 6171 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0029 | 0/0 | 6172 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0030 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0031 | 0/0 | 6172 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0002t0032 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0003t0005 | 0/0 | 6173 | 4 | 4 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6168): Show |
chr11 | 108003898 | 108112761 |
| a0001c0004t0012 | 0/0 | 6171 | 3 | 3 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0005t0016 | 0/0 | 6171 | 2 | 0 | 0 | 2 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0006t0001 | 0/0 | 6172 | 2 | 2 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0001c0007t0002 | 0/0 | 6171 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6166): Show |
chr11 | 108003898 | 108112761 |
| a0001c0009t0001 | 0/0 | 6172 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| a0002c0008t0001 | 0/0 | 6172 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | GCGCG others(6167): Show |
chr11 | 108003898 | 108112761 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0006g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0006g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0006g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0010g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0010g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0014g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0014g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0014g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0015g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0015g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0015g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0018g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0019g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0020g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0021g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0022g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0023g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0024g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0026g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0001t0028g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0007g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0007g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0008g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0008g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0008g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0008g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0011g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0011g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0011g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0013g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0013g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0017g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0025g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0027g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0029g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0030g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0031g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0002t0032g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0003t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0003t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0003t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0004t0012g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0004t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0005t0016g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0005t0016g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0006t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0006t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0007t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0001c0009t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| a0002c0008t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0047 | EUR | FIN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00423 | hp2 | a0001 | c0001 | t0024 | g0104 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00639 | hp1 | a0001 | c0002 | t0007 | g0049 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0286 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0174 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01069 | hp2 | a0001 | c0001 | t0014 | g0263 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01074 | hp1 | a0001 | c0002 | t0004 | g0073 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01074 | hp2 | a0001 | c0002 | t0007 | g0053 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0033 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0248 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01109 | hp1 | a0001 | c0002 | t0027 | g0217 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01109 | hp2 | a0001 | c0001 | t0014 | g0219 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0266 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01175 | hp1 | a0001 | c0001 | t0023 | g0296 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0224 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01243 | hp1 | a0001 | c0001 | t0021 | g0190 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01255 | hp2 | a0001 | c0001 | t0014 | g0264 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0044 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0237 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0186 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01515 | hp2 | a0001 | c0001 | t0015 | g0282 | EUR | IBS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0039 | EUR | IBS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0037 | EUR | IBS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01517 | hp2 | a0001 | c0001 | t0015 | g0245 | EUR | IBS | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0065 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01891 | hp2 | a0001 | c0006 | t0001 | g0115 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01981 | hp1 | a0001 | c0002 | t0008 | g0042 | AMR | PEL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02055 | hp2 | a0001 | c0002 | t0032 | g0062 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | PEL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0164 | AMR | PEL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02258 | hp1 | a0001 | c0002 | t0013 | g0203 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02451 | hp1 | a0001 | c0002 | t0009 | g0060 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02451 | hp2 | a0001 | c0002 | t0031 | g0086 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | KHV | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0170 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02572 | hp2 | a0001 | c0004 | t0012 | g0082 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0043 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0087 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02615 | hp1 | a0001 | c0002 | t0013 | g0204 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0080 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02622 | hp1 | a0001 | c0002 | t0013 | g0202 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02622 | hp2 | a0001 | c0002 | t0030 | g0302 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0076 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0212 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02647 | hp2 | a0001 | c0003 | t0005 | g0011 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0175 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02717 | hp1 | a0001 | c0004 | t0012 | g0005 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0056 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0196 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02818 | hp2 | a0001 | c0004 | t0012 | g0005 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0200 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02896 | hp1 | a0001 | c0003 | t0005 | g0001 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02896 | hp2 | a0001 | c0002 | t0009 | g0063 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02897 | hp1 | a0001 | c0003 | t0005 | g0001 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0199 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02922 | hp1 | a0001 | c0006 | t0001 | g0116 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0171 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0205 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02976 | hp2 | a0001 | c0002 | t0011 | g0197 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03098 | hp2 | a0001 | c0002 | t0005 | g0014 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03130 | hp1 | a0001 | c0002 | t0009 | g0059 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03130 | hp2 | a0001 | c0001 | t0020 | g0189 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0074 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0187 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03195 | hp2 | a0001 | c0002 | t0005 | g0015 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03209 | hp1 | a0001 | c0002 | t0025 | g0027 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03209 | hp2 | a0001 | c0007 | t0002 | g0207 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0051 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0172 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0081 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03486 | hp1 | a0001 | c0002 | t0009 | g0061 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0183 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03491 | hp1 | a0001 | c0002 | t0017 | g0178 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0184 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0198 | AFR | ESN | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03540 | hp2 | a0001 | c0003 | t0005 | g0012 | AFR | GWD | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0075 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0201 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03669 | hp1 | a0001 | c0002 | t0007 | g0050 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03688 | hp1 | a0001 | c0002 | t0008 | g0064 | SAS | STU | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0176 | SAS | STU | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03704 | hp2 | a0001 | c0001 | t0022 | g0275 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03710 | hp1 | a0001 | c0002 | t0008 | g0045 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0046 | SAS | BEB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0088 | SAS | BEB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18906 | hp1 | a0001 | c0002 | t0005 | g0016 | AFR | YRI | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | YRI | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18959 | hp1 | a0001 | c0001 | t0010 | g0144 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18959 | hp2 | a0001 | c0009 | t0001 | g0252 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0179 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18961 | hp1 | a0001 | c0001 | t0019 | g0097 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18970 | hp2 | a0001 | c0005 | t0016 | g0067 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18974 | hp2 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18981 | hp2 | a0001 | c0005 | t0016 | g0066 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18990 | hp2 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18993 | hp1 | a0001 | c0002 | t0011 | g0180 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19009 | hp2 | a0001 | c0001 | t0028 | g0154 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19030 | hp2 | a0001 | c0002 | t0011 | g0299 | AFR | LWK | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0168 | AFR | LWK | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19055 | hp1 | a0001 | c0001 | t0026 | g0103 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19077 | hp2 | a0001 | c0002 | t0029 | g0068 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0300 | AFR | YRI | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA19240 | hp2 | a0001 | c0002 | t0005 | g0013 | AFR | YRI | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA20129 | hp1 | a0001 | c0002 | t0008 | g0004 | AFR | ASW | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ASW | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0041 | EUR | TSI | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA20752 | hp2 | a0001 | c0002 | t0007 | g0052 | EUR | TSI | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA20905 | hp1 | a0001 | c0002 | t0007 | g0055 | SAS | GIH | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | GIH | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01123 | hp1 | a0001 | c0002 | t0003 | g0167 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG01123 | hp2 | a0002 | c0008 | t0001 | g0141 | AMR | CLM | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0169 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0208 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0071 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG02559 | hp2 | a0001 | c0002 | t0008 | g0004 | AFR | ACB | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0166 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG03471 | hp2 | a0001 | c0002 | t0010 | g0162 | AFR | MSL | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | USA | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0077 | AFR | USA | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA20300 | hp1 | a0001 | c0002 | t0011 | g0165 | AFR | USA | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA20300 | hp2 | a0001 | c0002 | t0009 | g0058 | AFR | USA | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0072 | AFR | LWK | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | LWK | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0281 | REF | REF | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0004 | g0206 | REF | REF | CUL5_chr11_108003898_108112761 | CUL5 | chr11 | 108003898 | 108112761 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108094457 | G | C | 1 | a0002 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.1510G>C | p.Glu504Gln | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 14/19 | 1961/6171 | 1510/2343 | 504/780 | chr11 | 108094457 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108046360 | A | G | 4 | a0001c0001 a0001c0006 a0001c0009 others(1): Show |
193 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
synonymous_variant | LOW | c.225A>G | p.Gln75Gln | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/19 | 676/6171 | 225/2343 | 75/780 | chr11 | 108046360 | |||
| chr11:108052776 | G | C | 1 | a0001c0007 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.528G>C | p.Leu176Leu | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/19 | 979/6171 | 528/2343 | 176/780 | chr11 | 108052776 | |||
| chr11:108072397 | T | C | 1 | a0001c0004 | 3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
synonymous_variant | LOW | c.940T>C | p.Leu314Leu | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 9/19 | 1391/6171 | 940/2343 | 314/780 | chr11 | 108072397 | |||
| chr11:108078178 | G | A | 1 | a0001c0005 | 2 | NA18970.hp2 NA18981.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1116G>A | p.Ala372Ala | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/19 | 1567/6171 | 1116/2343 | 372/780 | chr11 | 108078178 | |||
| chr11:108094912 | G | A | 1 | a0001c0003 | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.1668G>A | p.Pro556Pro | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 15/19 | 2119/6171 | 1668/2343 | 556/780 | chr11 | 108094912 | |||
| chr11:108095634 | T | C | 1 | a0001c0006 | 2 | HG01891.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.1848T>C | p.Phe616Phe | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/19 | 2299/6171 | 1848/2343 | 616/780 | chr11 | 108095634 | |||
| chr11:108095655 | T | A | 1 | a0001c0009 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.1869T>A | p.Thr623Thr | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/19 | 2320/6171 | 1869/2343 | 623/780 | chr11 | 108095655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108008994 | C | CA | 4 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0017 others(1): Show |
36 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-353dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/19 | 352 | INFO_REALIGN_3_PRIME | chr11 | 108008994 | |||||
| chr11:108104480 | T | A | 1 | a0001c0001t0019 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 96 | chr11 | 108104480 | ||||||
| chr11:108104480 | T | G | 1 | a0001c0001t0020 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 96 | chr11 | 108104480 | ||||||
| chr11:108104538 | A | G | 2 | a0001c0002t0009 a0001c0002t0032 |
6 | HG02055.hp2 HG02451.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*154A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 154 | chr11 | 108104538 | ||||||
| chr11:108104750 | G | A | 1 | a0001c0004t0012 | 3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*366G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 366 | chr11 | 108104750 | ||||||
| chr11:108104880 | A | G | 1 | a0001c0002t0009 | 5 | HG02451.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*496A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 496 | chr11 | 108104880 | ||||||
| chr11:108104926 | T | C | 1 | a0001c0002t0009 | 5 | HG02451.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*542T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 542 | chr11 | 108104926 | ||||||
| chr11:108105312 | A | T | 1 | a0001c0002t0031 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*928A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 928 | chr11 | 108105312 | ||||||
| chr11:108105388 | A | T | 11 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0007 others(8): Show |
59 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1004A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 1004 | chr11 | 108105388 | ||||||
| chr11:108105409 | C | T | 1 | a0001c0001t0028 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1025C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 1025 | chr11 | 108105409 | ||||||
| chr11:108105699 | A | T | 1 | a0001c0001t0015 | 3 | HG01261.hp2 HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1315A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 1315 | chr11 | 108105699 | ||||||
| chr11:108105723 | C | T | 3 | a0001c0002t0003 a0001c0002t0011 a0001c0002t0017 |
32 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1339C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 1339 | chr11 | 108105723 | ||||||
| chr11:108105825 | A | G | 1 | a0001c0002t0027 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1441A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 1441 | chr11 | 108105825 | ||||||
| chr11:108105891 | C | T | 1 | a0001c0001t0014 | 3 | HG01069.hp2 HG01109.hp2 HG01255.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1507C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 1507 | chr11 | 108105891 | ||||||
| chr11:108105896 | C | T | 1 | a0001c0002t0013 | 3 | HG02258.hp1 HG02615.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1512C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 1512 | chr11 | 108105896 | ||||||
| chr11:108105905 | T | C | 1 | a0001c0002t0017 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1521T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 1521 | chr11 | 108105905 | ||||||
| chr11:108106239 | A | G | 1 | a0001c0001t0026 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 1855 | chr11 | 108106239 | ||||||
| chr11:108106332 | T | C | 3 | a0001c0002t0003 a0001c0002t0011 a0001c0002t0017 |
32 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1948T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 1948 | chr11 | 108106332 | ||||||
| chr11:108106422 | A | C | 1 | a0001c0001t0006 | 5 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2038A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2038 | chr11 | 108106422 | ||||||
| chr11:108106536 | T | C | 1 | a0001c0001t0021 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2152T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2152 | chr11 | 108106536 | ||||||
| chr11:108106538 | CT | C | 30 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(27): Show |
274 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*2170delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2170 | INFO_REALIGN_3_PRIME | chr11 | 108106538 | |||||
| chr11:108106538 | CTT | C | 6 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0009 others(3): Show |
21 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2169_*2170delTT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2169 | INFO_REALIGN_3_PRIME | chr11 | 108106538 | |||||
| chr11:108106539 | T | G | 1 | a0001c0005t0016 | 2 | NA18970.hp2 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2155T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2155 | chr11 | 108106539 | ||||||
| chr11:108106556 | G | A | 1 | a0001c0001t0022 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2172G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2172 | chr11 | 108106556 | ||||||
| chr11:108106762 | G | A | 23 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(20): Show |
225 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*2378G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2378 | chr11 | 108106762 | ||||||
| chr11:108106836 | C | CA | 21 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(18): Show |
227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*2468dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2469 | INFO_REALIGN_3_PRIME | chr11 | 108106836 | |||||
| chr11:108106852 | A | T | 8 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0007 others(5): Show |
54 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2468A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2468 | chr11 | 108106852 | ||||||
| chr11:108106909 | C | T | 1 | a0001c0002t0008 | 5 | HG01981.hp1 HG02559.hp2 HG03688.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2525C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2525 | chr11 | 108106909 | ||||||
| chr11:108107022 | A | G | 1 | a0001c0001t0024 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2638A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2638 | chr11 | 108107022 | ||||||
| chr11:108107163 | C | T | 1 | a0001c0001t0023 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2779C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 2779 | chr11 | 108107163 | ||||||
| chr11:108107422 | G | T | 1 | a0001c0002t0007 | 5 | HG00639.hp1 HG01074.hp2 HG03669.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3038G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 3038 | chr11 | 108107422 | ||||||
| chr11:108107543 | A | G | 1 | a0001c0002t0025 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3159A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 3159 | chr11 | 108107543 | ||||||
| chr11:108107705 | T | TTTTATTT others(6): Show |
1 | a0001c0002t0017 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3324_*3336dupTATT others(9): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 19/19 | 3337 | INFO_REALIGN_3_PRIME | chr11 | 108107705 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108009375 | A | G | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.24+3A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108009375 | |||||||
| chr11:108009566 | G | A | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.24+194G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108009566 | |||||||
| chr11:108009570 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.24+198C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108009570 | |||||||
| chr11:108009611 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(8): Show |
12 | HG00280.hp2 HG01496.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+239G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108009611 | |||||||
| chr11:108009771 | A | G | 1 | a0001c0002t0004g0300 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.24+399A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108009771 | |||||||
| chr11:108009848 | C | G | 1 | a0001c0002t0011g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.24+476C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108009848 | |||||||
| chr11:108009914 | T | A | 1 | a0001c0002t0011g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.24+542T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108009914 | |||||||
| chr11:108009998 | T | C | 2 | a0001c0002t0004g0026 a0001c0002t0025g0027 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.24+626T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108009998 | |||||||
| chr11:108010031 | G | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02055.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.24+659G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010031 | |||||||
| chr11:108010154 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(92): Show |
100 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.24+782C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010154 | |||||||
| chr11:108010275 | C | T | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.24+903C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010275 | |||||||
| chr11:108010302 | C | T | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.24+930C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010302 | |||||||
| chr11:108010362 | T | C | 45 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(42): Show |
47 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.24+990T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010362 | |||||||
| chr11:108010397 | C | T | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+1025C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010397 | |||||||
| chr11:108010469 | C | G | 5 | a0001c0002t0002g0208 a0001c0002t0002g0209 a0001c0002t0002g0210 others(2): Show |
5 | HG01070.hp1 HG02109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+1097C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010469 | |||||||
| chr11:108010478 | A | G | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.24+1106A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010478 | |||||||
| chr11:108010599 | A | T | 1 | a0001c0002t0002g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.24+1227A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010599 | |||||||
| chr11:108010633 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.24+1261A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010633 | |||||||
| chr11:108010892 | T | G | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.24+1520T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108010892 | |||||||
| chr11:108011175 | G | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.24+1803G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011175 | |||||||
| chr11:108011262 | A | C | 1 | a0001c0002t0003g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.24+1890A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011262 | |||||||
| chr11:108011348 | G | A | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+1976G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011348 | |||||||
| chr11:108011428 | C | CG | 10 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0218 others(7): Show |
10 | HG00438.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.24+2060dupG | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108011428 | ||||||
| chr11:108011473 | A | G | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
4 | HG00738.hp1 HG01099.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+2101A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011473 | |||||||
| chr11:108011494 | A | T | 1 | a0001c0001t0002g0010 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.24+2122A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011494 | |||||||
| chr11:108011597 | A | G | 4 | a0001c0002t0002g0069 a0001c0002t0029g0068 a0001c0005t0016g0066 others(1): Show |
4 | HG02257.hp2 NA18970.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+2225A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011597 | |||||||
| chr11:108011628 | A | AT | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+2269dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108011628 | ||||||
| chr11:108011660 | G | T | 1 | a0001c0002t0003g0191 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.24+2288G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011660 | |||||||
| chr11:108011779 | C | T | 2 | a0001c0001t0020g0189 a0001c0001t0021g0190 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.24+2407C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011779 | |||||||
| chr11:108011819 | G | C | 67 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(64): Show |
70 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.24+2447G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011819 | |||||||
| chr11:108011839 | G | A | 2 | a0001c0002t0003g0087 a0001c0002t0003g0088 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.24+2467G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011839 | |||||||
| chr11:108011946 | G | A | 1 | a0001c0002t0001g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.24+2574G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011946 | |||||||
| chr11:108011972 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.24+2600C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108011972 | |||||||
| chr11:108012097 | T | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(180): Show |
189 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.24+2725T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012097 | |||||||
| chr11:108012178 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0023g0296 |
2 | HG01175.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.24+2806C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012178 | |||||||
| chr11:108012277 | T | A | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.24+2905T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012277 | |||||||
| chr11:108012294 | C | G | 1 | a0001c0002t0002g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.24+2922C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012294 | |||||||
| chr11:108012345 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.24+2973G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012345 | |||||||
| chr11:108012418 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.24+3046C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012418 | |||||||
| chr11:108012431 | C | G | 1 | a0001c0002t0008g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.24+3059C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012431 | |||||||
| chr11:108012509 | T | C | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.24+3137T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012509 | |||||||
| chr11:108012523 | CT | C | 105 | a0001c0001t0001g0025 a0001c0001t0001g0078 a0001c0001t0001g0090 others(102): Show |
107 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.24+3168delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108012523 | ||||||
| chr11:108012523 | CTT | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(96): Show |
104 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.24+3167_24+3168del others(2): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108012523 | ||||||
| chr11:108012526 | T | C | 1 | a0001c0001t0010g0224 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.24+3154T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012526 | |||||||
| chr11:108012653 | T | A | 30 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(27): Show |
30 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.24+3281T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012653 | |||||||
| chr11:108012683 | G | A | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.24+3311G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012683 | |||||||
| chr11:108012848 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.24+3476C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012848 | |||||||
| chr11:108012876 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
187 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.24+3504C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108012876 | |||||||
| chr11:108013017 | T | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(3): Show |
6 | NA18951.hp1 NA18984.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.24+3645T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108013017 | |||||||
| chr11:108013218 | C | T | 1 | a0001c0001t0021g0190 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.24+3846C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108013218 | |||||||
| chr11:108013519 | T | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.24+4147T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108013519 | |||||||
| chr11:108013547 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.24+4175A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108013547 | |||||||
| chr11:108013664 | C | A | 74 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0001g0089 others(71): Show |
75 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.24+4292C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108013664 | |||||||
| chr11:108013741 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.24+4369G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108013741 | |||||||
| chr11:108013959 | A | T | 1 | a0001c0002t0009g0063 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.24+4587A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108013959 | |||||||
| chr11:108014003 | C | T | 1 | a0001c0002t0003g0187 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.24+4631C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108014003 | |||||||
| chr11:108014097 | C | G | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.24+4725C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108014097 | |||||||
| chr11:108014472 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.24+5100G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108014472 | |||||||
| chr11:108014850 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG02055.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.24+5478A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108014850 | |||||||
| chr11:108014877 | C | T | 6 | a0001c0002t0009g0058 a0001c0002t0009g0059 a0001c0002t0009g0060 others(3): Show |
6 | HG02055.hp2 HG02451.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.24+5505C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108014877 | |||||||
| chr11:108014899 | A | T | 1 | a0001c0001t0001g0293 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.24+5527A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108014899 | |||||||
| chr11:108014902 | T | A | 30 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(27): Show |
30 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.24+5530T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108014902 | |||||||
| chr11:108014960 | A | G | 2 | a0001c0001t0001g0292 a0001c0001t0010g0224 |
2 | HG01175.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.24+5588A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108014960 | |||||||
| chr11:108014961 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.24+5589C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108014961 | |||||||
| chr11:108015265 | G | A | 18 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0035 others(15): Show |
20 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.24+5893G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108015265 | |||||||
| chr11:108015284 | A | C | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.24+5912A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108015284 | |||||||
| chr11:108015321 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0010g0224 |
2 | HG01175.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.24+5949G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108015321 | |||||||
| chr11:108015392 | G | A | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+6020G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108015392 | |||||||
| chr11:108015428 | T | A | 67 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(64): Show |
70 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.24+6056T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108015428 | |||||||
| chr11:108015512 | G | A | 2 | a0001c0002t0003g0087 a0001c0002t0003g0088 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.24+6140G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108015512 | |||||||
| chr11:108015668 | T | A | 30 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(27): Show |
30 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.24+6296T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108015668 | |||||||
| chr11:108015671 | A | C | 67 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(64): Show |
70 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.24+6299A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108015671 | |||||||
| chr11:108015802 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.24+6430T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108015802 | |||||||
| chr11:108015814 | G | A | 297 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(294): Show |
307 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.24+6442G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108015814 | |||||||
| chr11:108016106 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0293 |
2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.24+6734G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108016106 | |||||||
| chr11:108016140 | C | T | 6 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(3): Show |
6 | HG01081.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.24+6768C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108016140 | |||||||
| chr11:108016232 | T | TTTCTC | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG01192.hp2 NA18964.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.24+6876_24+6880dup others(5): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108016232 | ||||||
| chr11:108016232 | TTTCTC | T | 36 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(33): Show |
36 | HG00544.hp1 HG01070.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.24+6876_24+6880del others(5): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108016232 | ||||||
| chr11:108016495 | C | T | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+7123C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108016495 | |||||||
| chr11:108016548 | T | C | 50 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(47): Show |
52 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.24+7176T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108016548 | |||||||
| chr11:108016596 | G | T | 4 | a0001c0002t0003g0183 a0001c0002t0003g0184 a0001c0002t0003g0185 others(1): Show |
4 | HG01496.hp1 HG02523.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+7224G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108016596 | |||||||
| chr11:108016603 | G | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(217): Show |
227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.24+7231G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108016603 | |||||||
| chr11:108016797 | C | CA | 5 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
5 | HG00738.hp1 HG01099.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.24+7434dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108016797 | ||||||
| chr11:108016869 | A | G | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.24+7497A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108016869 | |||||||
| chr11:108016928 | T | C | 67 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(64): Show |
70 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.24+7556T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108016928 | |||||||
| chr11:108016958 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.24+7586C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108016958 | |||||||
| chr11:108017040 | G | A | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.24+7668G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108017040 | |||||||
| chr11:108017084 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 |
4 | HG01168.hp1 HG02683.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+7712A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108017084 | |||||||
| chr11:108017131 | G | C | 1 | a0001c0002t0011g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.24+7759G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108017131 | |||||||
| chr11:108017389 | C | CA | 148 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
157 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.24+8038dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108017389 | ||||||
| chr11:108017389 | C | CAA | 45 | a0001c0001t0001g0025 a0001c0001t0001g0227 a0001c0001t0001g0228 others(42): Show |
45 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.24+8037_24+8038dup others(2): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108017389 | ||||||
| chr11:108017389 | CA | C | 11 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(8): Show |
11 | HG01074.hp1 HG01109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.24+8038delA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108017389 | ||||||
| chr11:108017389 | CAAA | C | 63 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0001g0096 others(60): Show |
64 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.24+8036_24+8038del others(3): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108017389 | ||||||
| chr11:108017488 | T | C | 1 | a0001c0002t0003g0186 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.24+8116T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108017488 | |||||||
| chr11:108017536 | G | A | 38 | a0001c0001t0001g0009 a0001c0002t0003g0080 a0001c0002t0003g0087 others(35): Show |
40 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.24+8164G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108017536 | |||||||
| chr11:108017541 | C | G | 37 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(34): Show |
38 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.24+8169C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108017541 | |||||||
| chr11:108017587 | C | T | 2 | a0001c0002t0005g0015 a0001c0002t0005g0016 |
2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.24+8215C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108017587 | |||||||
| chr11:108017660 | G | A | 1 | a0001c0002t0003g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.24+8288G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108017660 | |||||||
| chr11:108017756 | A | G | 69 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(66): Show |
72 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.24+8384A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108017756 | |||||||
| chr11:108017826 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.24+8454G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108017826 | |||||||
| chr11:108018020 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.24+8648C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108018020 | |||||||
| chr11:108018311 | A | G | 4 | a0001c0002t0004g0199 a0001c0002t0004g0200 a0001c0002t0004g0201 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+8939A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108018311 | |||||||
| chr11:108018454 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02523.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.24+9082G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108018454 | |||||||
| chr11:108018504 | T | TA | 14 | a0001c0001t0001g0096 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
15 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.24+9145dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108018504 | ||||||
| chr11:108018566 | G | T | 287 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(284): Show |
297 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.24+9194G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108018566 | |||||||
| chr11:108018592 | T | C | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
4 | HG00738.hp1 HG01099.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+9220T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108018592 | |||||||
| chr11:108018683 | A | T | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.24+9311A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108018683 | |||||||
| chr11:108019143 | A | G | 28 | a0001c0001t0001g0009 a0001c0001t0001g0222 a0001c0001t0001g0225 others(25): Show |
30 | HG00558.hp1 HG00735.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.24+9771A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019143 | |||||||
| chr11:108019148 | A | G | 1 | a0001c0002t0002g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.24+9776A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019148 | |||||||
| chr11:108019193 | T | TGGGTGG | 13 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(10): Show |
13 | HG01074.hp1 HG01081.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.24+9836_24+9841dup others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108019193 | ||||||
| chr11:108019319 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24+9947A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019319 | |||||||
| chr11:108019384 | A | G | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.24+10012A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019384 | |||||||
| chr11:108019584 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.24+10212G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019584 | |||||||
| chr11:108019598 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.24+10226C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019598 | |||||||
| chr11:108019613 | C | T | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.24+10241C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019613 | |||||||
| chr11:108019665 | A | T | 2 | a0001c0001t0014g0263 a0001c0001t0014g0264 |
2 | HG01069.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.24+10293A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019665 | |||||||
| chr11:108019876 | C | T | 8 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.24+10504C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019876 | |||||||
| chr11:108019930 | C | T | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.24+10558C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019930 | |||||||
| chr11:108019931 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.24+10559G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019931 | |||||||
| chr11:108019967 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
194 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.24+10595A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108019967 | |||||||
| chr11:108020008 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.24+10636G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020008 | |||||||
| chr11:108020035 | C | T | 2 | a0001c0002t0004g0198 a0001c0002t0011g0197 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.24+10663C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020035 | |||||||
| chr11:108020075 | C | T | 10 | a0001c0002t0002g0051 a0001c0002t0002g0054 a0001c0002t0002g0056 others(7): Show |
10 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.24+10703C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020075 | |||||||
| chr11:108020141 | C | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG02135.hp2 NA18945.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.24+10769C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020141 | |||||||
| chr11:108020283 | A | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.24+10911A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020283 | |||||||
| chr11:108020306 | G | A | 2 | a0001c0002t0004g0199 a0001c0002t0004g0200 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.24+10934G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020306 | |||||||
| chr11:108020327 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
103 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.24+10955G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020327 | |||||||
| chr11:108020535 | A | AT | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
195 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.24+11176dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108020535 | ||||||
| chr11:108020542 | T | G | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.24+11170T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020542 | |||||||
| chr11:108020544 | T | TG | 4 | a0001c0001t0001g0287 a0001c0002t0030g0302 a0001c0006t0001g0115 others(1): Show |
4 | HG01168.hp1 HG01891.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+11172_24+11173i others(3): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020544 | |||||||
| chr11:108020545 | T | G | 1 | a0001c0002t0002g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.24+11173T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020545 | |||||||
| chr11:108020584 | G | A | 1 | a0001c0002t0001g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.24+11212G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020584 | |||||||
| chr11:108020588 | C | G | 1 | a0001c0001t0001g0007 | 2 | HG00423.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.24+11216C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020588 | |||||||
| chr11:108020662 | G | A | 2 | a0001c0002t0004g0201 a0001c0002t0004g0300 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.24+11290G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108020662 | |||||||
| chr11:108021165 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.24+11793T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108021165 | |||||||
| chr11:108021266 | T | G | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.24+11894T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108021266 | |||||||
| chr11:108021554 | A | C | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.24+12182A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108021554 | |||||||
| chr11:108021624 | A | G | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.25-12178A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108021624 | |||||||
| chr11:108021685 | T | A | 1 | a0001c0001t0001g0079 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.25-12117T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108021685 | |||||||
| chr11:108021730 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
233 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.25-12072A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108021730 | |||||||
| chr11:108021813 | GTTTA | G | 23 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(20): Show |
25 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.25-11977_25-11974d others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108021813 | ||||||
| chr11:108021994 | A | G | 1 | a0001c0002t0002g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.25-11808A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108021994 | |||||||
| chr11:108022013 | G | A | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-11789G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108022013 | |||||||
| chr11:108022094 | C | CTTGGTCT others(6): Show |
188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
194 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.25-11708_25-11707i others(15): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108022094 | |||||||
| chr11:108022153 | C | T | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.25-11649C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108022153 | |||||||
| chr11:108022190 | A | T | 1 | a0001c0001t0001g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.25-11612A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108022190 | |||||||
| chr11:108022245 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.25-11557G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108022245 | |||||||
| chr11:108022259 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0284 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.25-11543A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108022259 | |||||||
| chr11:108022441 | A | G | 3 | a0001c0002t0004g0198 a0001c0002t0011g0197 a0001c0007t0002g0207 |
3 | HG02976.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.25-11361A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108022441 | |||||||
| chr11:108022504 | TG | T | 10 | a0001c0002t0002g0051 a0001c0002t0002g0054 a0001c0002t0002g0056 others(7): Show |
10 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.25-11293delG | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108022504 | ||||||
| chr11:108022630 | C | T | 1 | a0001c0002t0002g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.25-11172C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108022630 | |||||||
| chr11:108022893 | A | T | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-10909A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108022893 | |||||||
| chr11:108022977 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.25-10825G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108022977 | |||||||
| chr11:108023094 | A | T | 297 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(294): Show |
307 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.25-10708A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108023094 | |||||||
| chr11:108023099 | C | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.25-10703C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108023099 | |||||||
| chr11:108023544 | G | GA | 45 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(42): Show |
47 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.25-10250dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108023544 | ||||||
| chr11:108023586 | A | G | 23 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(20): Show |
25 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.25-10216A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108023586 | |||||||
| chr11:108023655 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(90): Show |
98 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.25-10147A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108023655 | |||||||
| chr11:108023982 | G | A | 1 | a0001c0002t0003g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.25-9820G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108023982 | |||||||
| chr11:108024036 | A | G | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.25-9766A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108024036 | |||||||
| chr11:108024089 | G | A | 1 | a0001c0002t0003g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.25-9713G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108024089 | |||||||
| chr11:108024201 | C | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.25-9601C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108024201 | |||||||
| chr11:108024426 | AAAT | A | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.25-9358_25-9356del others(3): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108024426 | ||||||
| chr11:108024429 | T | A | 5 | a0001c0002t0009g0058 a0001c0002t0009g0059 a0001c0002t0009g0060 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-9373T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108024429 | |||||||
| chr11:108024542 | G | T | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-9260G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108024542 | |||||||
| chr11:108024626 | A | C | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25-9176A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108024626 | |||||||
| chr11:108024762 | G | T | 2 | a0001c0002t0004g0198 a0001c0002t0011g0197 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.25-9040G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108024762 | |||||||
| chr11:108024948 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.25-8854C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108024948 | |||||||
| chr11:108025024 | T | A | 1 | a0001c0002t0003g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.25-8778T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108025024 | |||||||
| chr11:108025110 | C | G | 298 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
308 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.25-8692C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108025110 | |||||||
| chr11:108025381 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.25-8421G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108025381 | |||||||
| chr11:108025509 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.25-8293T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108025509 | |||||||
| chr11:108025510 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.25-8292C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108025510 | |||||||
| chr11:108025517 | G | T | 2 | a0001c0002t0001g0084 a0001c0002t0001g0085 |
2 | HG01081.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.25-8285G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108025517 | |||||||
| chr11:108025880 | T | G | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-7922T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108025880 | |||||||
| chr11:108025929 | C | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
193 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.25-7873C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108025929 | |||||||
| chr11:108025962 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.25-7840G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108025962 | |||||||
| chr11:108026039 | A | G | 2 | a0001c0002t0004g0026 a0001c0002t0025g0027 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.25-7763A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108026039 | |||||||
| chr11:108026088 | C | T | 1 | a0001c0002t0002g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.25-7714C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108026088 | |||||||
| chr11:108026159 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
193 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.25-7643C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108026159 | |||||||
| chr11:108026584 | C | G | 1 | a0001c0001t0001g0280 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.25-7218C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108026584 | |||||||
| chr11:108026613 | G | A | 1 | a0001c0002t0003g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.25-7189G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108026613 | |||||||
| chr11:108026823 | T | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.25-6979T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108026823 | |||||||
| chr11:108026921 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
4 | HG00738.hp1 HG01099.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-6881G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108026921 | |||||||
| chr11:108026946 | G | A | 5 | a0001c0002t0002g0208 a0001c0002t0002g0209 a0001c0002t0002g0210 others(2): Show |
5 | HG01070.hp1 HG02109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-6856G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108026946 | |||||||
| chr11:108026981 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.25-6821T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108026981 | |||||||
| chr11:108026988 | C | CA | 9 | a0001c0001t0001g0018 a0001c0001t0001g0133 a0001c0001t0001g0160 others(6): Show |
9 | HG00408.hp2 HG00741.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.25-6795dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108026988 | ||||||
| chr11:108026988 | CA | C | 82 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0002t0001g0081 others(79): Show |
86 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.25-6795delA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108026988 | ||||||
| chr11:108026988 | CAA | C | 12 | a0001c0002t0003g0087 a0001c0002t0003g0088 a0001c0002t0003g0163 others(9): Show |
12 | HG02572.hp2 HG02602.hp2 HG03491.hp1 others(9): Show |
intron_variant | MODIFIER | c.25-6796_25-6795del others(2): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108026988 | ||||||
| chr11:108027273 | AT | A | 33 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(30): Show |
35 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.25-6515delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108027273 | ||||||
| chr11:108027331 | G | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0258 |
3 | HG00423.hp1 NA18961.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.25-6471G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108027331 | |||||||
| chr11:108027524 | G | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.25-6278G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108027524 | |||||||
| chr11:108027687 | A | G | 1 | a0001c0002t0004g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.25-6115A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108027687 | |||||||
| chr11:108027698 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.25-6104C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108027698 | |||||||
| chr11:108027751 | A | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.25-6051A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108027751 | |||||||
| chr11:108027795 | A | G | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.25-6007A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108027795 | |||||||
| chr11:108027925 | C | G | 1 | a0001c0002t0002g0070 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.25-5877C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108027925 | |||||||
| chr11:108028220 | A | T | 1 | a0001c0001t0001g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.25-5582A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108028220 | |||||||
| chr11:108028255 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
193 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.25-5547C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108028255 | |||||||
| chr11:108028597 | C | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
309 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.25-5205C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108028597 | |||||||
| chr11:108028628 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0293 |
2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25-5174C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108028628 | |||||||
| chr11:108028649 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(3): Show |
7 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-5153C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108028649 | |||||||
| chr11:108028696 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.25-5106C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108028696 | |||||||
| chr11:108028840 | A | T | 1 | a0001c0001t0001g0220 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25-4962A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108028840 | |||||||
| chr11:108028871 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.25-4931C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108028871 | |||||||
| chr11:108028915 | T | G | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.25-4887T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108028915 | |||||||
| chr11:108029113 | G | A | 2 | a0001c0002t0002g0041 a0001c0002t0002g0065 |
2 | HG01884.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.25-4689G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108029113 | |||||||
| chr11:108029155 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.25-4647A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108029155 | |||||||
| chr11:108029258 | G | T | 1 | a0001c0002t0002g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.25-4544G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108029258 | |||||||
| chr11:108029269 | G | C | 1 | a0001c0001t0001g0220 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25-4533G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108029269 | |||||||
| chr11:108029389 | C | G | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-4413C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108029389 | |||||||
| chr11:108029504 | C | T | 1 | a0001c0001t0001g0017 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.25-4298C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108029504 | |||||||
| chr11:108029856 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0019g0097 |
2 | NA18955.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.25-3946T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108029856 | |||||||
| chr11:108029872 | G | C | 23 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(20): Show |
25 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.25-3930G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108029872 | |||||||
| chr11:108029925 | G | C | 277 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
287 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.25-3877G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108029925 | |||||||
| chr11:108029981 | G | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0098 others(44): Show |
48 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.25-3821G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108029981 | |||||||
| chr11:108030041 | T | A | 1 | a0001c0001t0020g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.25-3761T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030041 | |||||||
| chr11:108030070 | G | A | 2 | a0001c0002t0003g0183 a0001c0002t0003g0184 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.25-3732G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030070 | |||||||
| chr11:108030544 | G | A | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG00738.hp1 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.25-3258G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030544 | |||||||
| chr11:108030549 | A | G | 2 | a0001c0002t0004g0198 a0001c0002t0011g0197 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.25-3253A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030549 | |||||||
| chr11:108030611 | T | G | 1 | a0001c0001t0001g0133 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.25-3191T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030611 | |||||||
| chr11:108030710 | G | A | 1 | a0001c0002t0002g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.25-3092G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030710 | |||||||
| chr11:108030716 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.25-3086A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030716 | |||||||
| chr11:108030765 | G | T | 5 | a0001c0001t0001g0228 a0001c0001t0001g0250 a0001c0001t0001g0251 others(2): Show |
5 | NA18959.hp2 NA18998.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-3037G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030765 | |||||||
| chr11:108030908 | A | G | 2 | a0001c0002t0004g0198 a0001c0002t0011g0197 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.25-2894A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030908 | |||||||
| chr11:108030939 | G | A | 2 | a0001c0006t0001g0115 a0001c0006t0001g0116 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.25-2863G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030939 | |||||||
| chr11:108030950 | T | G | 31 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(28): Show |
31 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.25-2852T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108030950 | |||||||
| chr11:108031019 | T | C | 1 | a0001c0002t0011g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25-2783T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031019 | |||||||
| chr11:108031186 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.25-2616G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031186 | |||||||
| chr11:108031199 | C | T | 1 | a0001c0001t0028g0154 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.25-2603C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031199 | |||||||
| chr11:108031287 | C | A | 2 | a0001c0002t0002g0040 a0001c0002t0002g0047 |
2 | HG00280.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.25-2515C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031287 | |||||||
| chr11:108031291 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
97 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.25-2511G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031291 | |||||||
| chr11:108031311 | G | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.25-2491G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031311 | |||||||
| chr11:108031334 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25-2468C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031334 | |||||||
| chr11:108031364 | C | CA | 11 | a0001c0002t0002g0034 a0001c0002t0004g0198 a0001c0002t0009g0058 others(8): Show |
11 | HG02145.hp2 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-2422dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108031364 | ||||||
| chr11:108031364 | CA | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
283 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.25-2422delA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108031364 | ||||||
| chr11:108031488 | G | A | 4 | a0001c0002t0003g0080 a0001c0002t0003g0166 a0001c0002t0003g0167 others(1): Show |
4 | HG01123.hp1 HG02615.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-2314G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031488 | |||||||
| chr11:108031565 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.25-2237G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031565 | |||||||
| chr11:108031782 | A | G | 4 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0038 others(1): Show |
4 | HG00642.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-2020A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031782 | |||||||
| chr11:108031799 | G | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0292 a0001c0001t0010g0224 |
3 | HG01175.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.25-2003G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031799 | |||||||
| chr11:108031951 | T | C | 1 | a0001c0002t0002g0208 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25-1851T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031951 | |||||||
| chr11:108031986 | A | G | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-1816A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108031986 | |||||||
| chr11:108032169 | A | C | 1 | a0001c0002t0002g0208 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25-1633A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108032169 | |||||||
| chr11:108032183 | C | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
5 | HG01168.hp1 HG01192.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-1619C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108032183 | |||||||
| chr11:108032204 | C | T | 282 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(279): Show |
292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.25-1598C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108032204 | |||||||
| chr11:108032225 | G | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0284 a0001c0001t0006g0248 |
3 | HG01106.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.25-1577G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108032225 | |||||||
| chr11:108032258 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0010g0224 |
2 | HG01175.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.25-1544G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108032258 | |||||||
| chr11:108032379 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.25-1423G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108032379 | |||||||
| chr11:108032581 | G | GTC | 12 | a0001c0002t0002g0048 a0001c0002t0002g0208 a0001c0002t0002g0209 others(9): Show |
12 | HG01070.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.25-1201_25-1200dup others(2): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 108032581 | ||||||
| chr11:108032591 | C | G | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.25-1211C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108032591 | |||||||
| chr11:108032601 | C | T | 225 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
232 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.25-1201C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108032601 | |||||||
| chr11:108032637 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG00408.hp2 NA18972.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.25-1165A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108032637 | |||||||
| chr11:108032801 | G | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
6 | HG00423.hp1 NA18948.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.25-1001G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108032801 | |||||||
| chr11:108033068 | A | G | 1 | a0001c0002t0002g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.25-734A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108033068 | |||||||
| chr11:108033653 | C | T | 24 | a0001c0001t0001g0006 a0001c0001t0001g0118 a0001c0001t0001g0119 others(21): Show |
25 | HG00438.hp2 HG02027.hp1 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.25-149C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108033653 | |||||||
| chr11:108033793 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.25-9T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 1/18 | chr11 | 108033793 | |||||||
| chr11:108033920 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
193 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.134+9C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108033920 | |||||||
| chr11:108033972 | A | C | 8 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.134+61A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108033972 | |||||||
| chr11:108034107 | T | C | 2 | a0001c0002t0002g0041 a0001c0002t0002g0065 |
2 | HG01884.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.134+196T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108034107 | |||||||
| chr11:108034187 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
5 | HG01168.hp1 HG01192.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.134+276G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108034187 | |||||||
| chr11:108034239 | C | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+328C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108034239 | |||||||
| chr11:108034283 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.134+372A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108034283 | |||||||
| chr11:108034387 | C | T | 2 | a0001c0001t0015g0245 a0001c0001t0015g0282 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.134+476C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108034387 | |||||||
| chr11:108034541 | G | C | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.134+630G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108034541 | |||||||
| chr11:108034683 | A | G | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.134+772A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108034683 | |||||||
| chr11:108034883 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.134+972G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108034883 | |||||||
| chr11:108035015 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
193 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.134+1104T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035015 | |||||||
| chr11:108035072 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.134+1161G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035072 | |||||||
| chr11:108035112 | G | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+1201G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035112 | |||||||
| chr11:108035127 | A | G | 1 | a0001c0009t0001g0252 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.134+1216A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035127 | |||||||
| chr11:108035298 | C | A | 1 | a0001c0001t0001g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.134+1387C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035298 | |||||||
| chr11:108035300 | A | C | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.134+1389A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035300 | |||||||
| chr11:108035393 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.134+1482G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035393 | |||||||
| chr11:108035455 | G | A | 1 | a0001c0002t0002g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.134+1544G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035455 | |||||||
| chr11:108035540 | C | G | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.134+1629C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035540 | |||||||
| chr11:108035574 | T | TA | 6 | a0001c0001t0001g0091 a0001c0001t0001g0129 a0001c0001t0020g0189 others(3): Show |
6 | HG01074.hp1 HG01256.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.134+1680dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108035574 | ||||||
| chr11:108035574 | TA | T | 50 | a0001c0001t0001g0031 a0001c0001t0001g0109 a0001c0001t0001g0231 others(47): Show |
52 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.134+1680delA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108035574 | ||||||
| chr11:108035604 | G | A | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.134+1693G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035604 | |||||||
| chr11:108035700 | A | G | 1 | a0001c0001t0028g0154 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.134+1789A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035700 | |||||||
| chr11:108035726 | G | C | 1 | a0001c0002t0004g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.134+1815G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035726 | |||||||
| chr11:108035758 | A | G | 1 | a0001c0002t0004g0205 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.134+1847A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035758 | |||||||
| chr11:108035985 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.134+2074C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035985 | |||||||
| chr11:108035986 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02523.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.134+2075G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108035986 | |||||||
| chr11:108036012 | C | T | 1 | a0001c0002t0003g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.134+2101C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108036012 | |||||||
| chr11:108036179 | C | G | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.134+2268C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108036179 | |||||||
| chr11:108036199 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.134+2288C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108036199 | |||||||
| chr11:108036260 | T | C | 1 | a0001c0002t0002g0035 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.134+2349T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108036260 | |||||||
| chr11:108036262 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.134+2351T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108036262 | |||||||
| chr11:108036638 | A | G | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.134+2727A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108036638 | |||||||
| chr11:108036678 | A | G | 12 | a0001c0002t0002g0048 a0001c0002t0002g0208 a0001c0002t0002g0209 others(9): Show |
12 | HG01070.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.134+2767A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108036678 | |||||||
| chr11:108036719 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.134+2808C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108036719 | |||||||
| chr11:108036871 | T | C | 5 | a0001c0002t0004g0198 a0001c0002t0011g0197 a0001c0002t0013g0202 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.134+2960T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108036871 | |||||||
| chr11:108037098 | C | T | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.134+3187C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108037098 | |||||||
| chr11:108037101 | C | T | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.134+3190C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108037101 | |||||||
| chr11:108037215 | A | G | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134+3304A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108037215 | |||||||
| chr11:108037230 | A | G | 1 | a0001c0001t0006g0008 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.134+3319A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108037230 | |||||||
| chr11:108037653 | G | C | 1 | a0001c0001t0006g0008 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.134+3742G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108037653 | |||||||
| chr11:108037660 | A | G | 23 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(20): Show |
25 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.134+3749A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108037660 | |||||||
| chr11:108037690 | TG | T | 4 | a0001c0001t0001g0101 a0001c0002t0004g0072 a0001c0002t0004g0073 others(1): Show |
4 | HG01074.hp1 HG03139.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.134+3784delG | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108037690 | ||||||
| chr11:108037983 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.134+4072A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108037983 | |||||||
| chr11:108037991 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.134+4080C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108037991 | |||||||
| chr11:108038057 | A | G | 5 | a0001c0002t0004g0198 a0001c0002t0011g0197 a0001c0002t0013g0202 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.134+4146A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108038057 | |||||||
| chr11:108038224 | ATGT | A | 23 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(20): Show |
25 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.134+4318_134+4320d others(5): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108038224 | ||||||
| chr11:108038485 | C | T | 7 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG00733.hp2 HG00735.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.134+4574C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108038485 | |||||||
| chr11:108038535 | T | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
193 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.134+4624T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108038535 | |||||||
| chr11:108038567 | T | C | 5 | a0001c0002t0002g0208 a0001c0002t0002g0209 a0001c0002t0002g0210 others(2): Show |
5 | HG01070.hp1 HG02109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.134+4656T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108038567 | |||||||
| chr11:108038652 | G | A | 1 | a0001c0002t0004g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.134+4741G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108038652 | |||||||
| chr11:108038677 | G | GA | 12 | a0001c0001t0001g0235 a0001c0001t0021g0190 a0001c0002t0002g0051 others(9): Show |
12 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.134+4782dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108038677 | ||||||
| chr11:108038886 | TTGAC | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+4979_134+4982d others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108038886 | ||||||
| chr11:108039356 | T | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0098 others(45): Show |
49 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.134+5445T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108039356 | |||||||
| chr11:108039482 | C | G | 8 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.134+5571C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108039482 | |||||||
| chr11:108039584 | G | A | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.134+5673G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108039584 | |||||||
| chr11:108039712 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0258 |
3 | HG00423.hp1 NA18961.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.134+5801A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108039712 | |||||||
| chr11:108039791 | A | G | 1 | a0001c0002t0003g0182 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.134+5880A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108039791 | |||||||
| chr11:108039838 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.134+5927T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108039838 | |||||||
| chr11:108039849 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.134+5938T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108039849 | |||||||
| chr11:108039926 | G | A | 10 | a0001c0002t0002g0051 a0001c0002t0002g0054 a0001c0002t0002g0056 others(7): Show |
10 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.134+6015G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108039926 | |||||||
| chr11:108039936 | G | T | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.134+6025G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108039936 | |||||||
| chr11:108040088 | T | C | 3 | a0001c0002t0013g0202 a0001c0002t0013g0203 a0001c0002t0013g0204 |
3 | HG02258.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.134+6177T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040088 | |||||||
| chr11:108040125 | A | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0226 a0001c0001t0001g0246 others(3): Show |
7 | HG00423.hp1 HG00544.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.135-6145A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040125 | |||||||
| chr11:108040164 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
193 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.135-6106C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040164 | |||||||
| chr11:108040231 | A | G | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135-6039A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040231 | |||||||
| chr11:108040251 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0285 |
2 | NA18986.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.135-6019T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040251 | |||||||
| chr11:108040347 | C | T | 1 | a0001c0002t0002g0212 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.135-5923C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040347 | |||||||
| chr11:108040360 | C | G | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-5910C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040360 | |||||||
| chr11:108040376 | C | T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0256 others(1): Show |
5 | HG01891.hp1 HG02145.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-5894C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040376 | |||||||
| chr11:108040520 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.135-5750G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040520 | |||||||
| chr11:108040611 | C | CA | 29 | a0001c0002t0003g0163 a0001c0002t0003g0164 a0001c0002t0003g0173 others(26): Show |
31 | HG00741.hp2 HG01496.hp1 HG02148.hp2 others(28): Show |
intron_variant | MODIFIER | c.135-5635dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108040611 | ||||||
| chr11:108040611 | C | CAA | 14 | a0001c0002t0002g0070 a0001c0002t0003g0080 a0001c0002t0003g0087 others(11): Show |
14 | HG01123.hp1 HG02572.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.135-5636_135-5635d others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108040611 | ||||||
| chr11:108040611 | C | CAAA | 19 | a0001c0002t0002g0048 a0001c0002t0002g0054 a0001c0002t0002g0056 others(16): Show |
19 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.135-5637_135-5635d others(5): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108040611 | ||||||
| chr11:108040611 | C | CAAAA | 20 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(17): Show |
22 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.135-5638_135-5635d others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108040611 | ||||||
| chr11:108040611 | C | CAAAAA | 7 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0043 others(4): Show |
7 | HG01261.hp1 HG01517.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.135-5639_135-5635d others(7): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108040611 | ||||||
| chr11:108040611 | CA | C | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.135-5635delA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108040611 | ||||||
| chr11:108040611 | CAAAAA | C | 18 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0120 others(15): Show |
19 | HG00438.hp1 HG01175.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.135-5639_135-5635d others(7): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108040611 | ||||||
| chr11:108040611 | CAAAAAA | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
174 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.135-5640_135-5635d others(8): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108040611 | ||||||
| chr11:108040709 | A | G | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.135-5561A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040709 | |||||||
| chr11:108040724 | C | T | 7 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG00733.hp2 HG00735.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.135-5546C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040724 | |||||||
| chr11:108040756 | G | A | 6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | NA18939.hp2 NA18951.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.135-5514G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040756 | |||||||
| chr11:108040925 | T | C | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.135-5345T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108040925 | |||||||
| chr11:108041108 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.135-5162C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041108 | |||||||
| chr11:108041131 | G | C | 1 | a0001c0002t0007g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.135-5139G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041131 | |||||||
| chr11:108041140 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.135-5130C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041140 | |||||||
| chr11:108041228 | C | T | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.135-5042C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041228 | |||||||
| chr11:108041285 | C | CT | 15 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0021g0190 others(12): Show |
15 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.135-4971dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108041285 | ||||||
| chr11:108041323 | G | A | 78 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0078 others(75): Show |
79 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.135-4947G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041323 | |||||||
| chr11:108041557 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.135-4713A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041557 | |||||||
| chr11:108041578 | G | A | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.135-4692G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041578 | |||||||
| chr11:108041645 | C | T | 1 | a0001c0002t0002g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.135-4625C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041645 | |||||||
| chr11:108041659 | C | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-4611C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041659 | |||||||
| chr11:108041764 | G | A | 45 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(42): Show |
47 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.135-4506G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041764 | |||||||
| chr11:108041811 | C | T | 1 | a0001c0001t0020g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.135-4459C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041811 | |||||||
| chr11:108041881 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.135-4389C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041881 | |||||||
| chr11:108041978 | T | C | 3 | a0001c0002t0003g0183 a0001c0002t0003g0184 a0001c0002t0003g0186 |
3 | HG01496.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.135-4292T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108041978 | |||||||
| chr11:108042004 | G | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.135-4266G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042004 | |||||||
| chr11:108042189 | C | T | 2 | a0001c0001t0020g0189 a0001c0001t0021g0190 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.135-4081C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042189 | |||||||
| chr11:108042218 | C | CT | 203 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
208 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.135-4033dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108042218 | ||||||
| chr11:108042218 | C | CTT | 38 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0079 others(35): Show |
41 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.135-4034_135-4033d others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108042218 | ||||||
| chr11:108042218 | C | CTTT | 8 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0002t0002g0051 others(5): Show |
9 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.135-4035_135-4033d others(5): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108042218 | ||||||
| chr11:108042218 | CTTTTT | C | 36 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(33): Show |
37 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.135-4037_135-4033d others(7): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108042218 | ||||||
| chr11:108042289 | G | A | 1 | a0001c0002t0025g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.135-3981G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042289 | |||||||
| chr11:108042353 | G | A | 4 | a0001c0002t0004g0199 a0001c0002t0004g0200 a0001c0002t0004g0201 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-3917G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042353 | |||||||
| chr11:108042411 | G | A | 2 | a0001c0002t0002g0036 a0001c0002t0002g0038 |
2 | HG00642.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.135-3859G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042411 | |||||||
| chr11:108042425 | T | A | 4 | a0001c0002t0004g0199 a0001c0002t0004g0200 a0001c0002t0004g0201 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-3845T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042425 | |||||||
| chr11:108042712 | T | G | 2 | a0001c0006t0001g0115 a0001c0006t0001g0116 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.135-3558T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042712 | |||||||
| chr11:108042848 | C | T | 1 | a0001c0002t0029g0068 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.135-3422C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042848 | |||||||
| chr11:108042849 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.135-3421G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042849 | |||||||
| chr11:108042886 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
233 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.135-3384T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042886 | |||||||
| chr11:108042902 | AC | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
97 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.135-3367delC | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108042902 | |||||||
| chr11:108043112 | G | A | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.135-3158G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108043112 | |||||||
| chr11:108043156 | C | T | 282 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(279): Show |
292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.135-3114C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108043156 | |||||||
| chr11:108043157 | T | C | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.135-3113T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108043157 | |||||||
| chr11:108043244 | A | G | 1 | a0001c0002t0004g0026 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.135-3026A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108043244 | |||||||
| chr11:108043345 | A | T | 2 | a0001c0002t0004g0071 a0001c0002t0004g0077 |
2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.135-2925A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108043345 | |||||||
| chr11:108043360 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.135-2910C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108043360 | |||||||
| chr11:108043566 | G | A | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.135-2704G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108043566 | |||||||
| chr11:108043664 | A | G | 27 | a0001c0001t0001g0019 a0001c0001t0001g0078 a0001c0001t0001g0089 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.135-2606A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108043664 | |||||||
| chr11:108043870 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.135-2400A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108043870 | |||||||
| chr11:108043936 | T | C | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-2334T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108043936 | |||||||
| chr11:108044039 | A | G | 1 | a0001c0002t0001g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.135-2231A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108044039 | |||||||
| chr11:108044142 | T | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0098 others(46): Show |
50 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.135-2128T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108044142 | |||||||
| chr11:108044190 | G | C | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-2080G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108044190 | |||||||
| chr11:108044507 | CA | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
192 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.135-1750delA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108044507 | ||||||
| chr11:108044523 | A | G | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.135-1747A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108044523 | |||||||
| chr11:108044536 | A | G | 2 | a0001c0002t0005g0015 a0001c0002t0005g0016 |
2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.135-1734A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108044536 | |||||||
| chr11:108044740 | C | CT | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.135-1520dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 108044740 | ||||||
| chr11:108044843 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG02486.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.135-1427C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108044843 | |||||||
| chr11:108044848 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.135-1422G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108044848 | |||||||
| chr11:108044916 | C | T | 7 | a0001c0002t0003g0080 a0001c0002t0003g0166 a0001c0002t0003g0167 others(4): Show |
7 | HG01123.hp1 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.135-1354C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108044916 | |||||||
| chr11:108044919 | G | T | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.135-1351G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108044919 | |||||||
| chr11:108045102 | T | A | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.135-1168T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108045102 | |||||||
| chr11:108045135 | A | C | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.135-1135A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108045135 | |||||||
| chr11:108045379 | G | A | 1 | a0001c0002t0003g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.135-891G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108045379 | |||||||
| chr11:108045624 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.135-646G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108045624 | |||||||
| chr11:108045699 | C | T | 1 | a0001c0001t0014g0264 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.135-571C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108045699 | |||||||
| chr11:108045750 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.135-520C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108045750 | |||||||
| chr11:108045880 | A | T | 1 | a0001c0001t0002g0254 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.135-390A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108045880 | |||||||
| chr11:108046050 | C | T | 1 | a0001c0001t0028g0154 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.135-220C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 2/18 | chr11 | 108046050 | |||||||
| chr11:108046443 | T | C | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+74T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108046443 | |||||||
| chr11:108046580 | A | G | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+211A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108046580 | |||||||
| chr11:108046607 | A | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+238A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108046607 | |||||||
| chr11:108047372 | A | G | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+1003A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108047372 | |||||||
| chr11:108047381 | T | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.234+1012T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108047381 | |||||||
| chr11:108047514 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.234+1145A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108047514 | |||||||
| chr11:108047803 | T | C | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234+1434T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108047803 | |||||||
| chr11:108047827 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG02486.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.234+1458A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108047827 | |||||||
| chr11:108047835 | T | G | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+1466T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108047835 | |||||||
| chr11:108048172 | A | G | 27 | a0001c0001t0001g0019 a0001c0001t0001g0078 a0001c0001t0001g0089 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.235-1718A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108048172 | |||||||
| chr11:108048173 | C | A | 1 | a0001c0002t0002g0035 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.235-1717C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108048173 | |||||||
| chr11:108048367 | A | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(293): Show |
306 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.235-1523A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108048367 | |||||||
| chr11:108048397 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
193 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.235-1493G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108048397 | |||||||
| chr11:108048608 | C | G | 1 | a0001c0002t0003g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.235-1282C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108048608 | |||||||
| chr11:108048648 | C | CTT | 12 | a0001c0002t0001g0081 a0001c0002t0004g0071 a0001c0002t0004g0072 others(9): Show |
13 | HG01074.hp1 HG02486.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.235-1207_235-1206d others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | C | CTTTT | 7 | a0001c0002t0003g0163 a0001c0002t0003g0177 a0001c0002t0003g0179 others(4): Show |
7 | HG03491.hp1 NA18939.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-1209_235-1206d others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | C | CTTTTT | 7 | a0001c0002t0001g0084 a0001c0002t0001g0085 a0001c0002t0003g0087 others(4): Show |
7 | HG01081.hp2 HG02280.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-1210_235-1206d others(7): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | C | CTTTTTTT others(4): Show |
1 | a0001c0002t0003g0187 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.235-1216_235-1206d others(13): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | C | CTTTTTTT others(5): Show |
7 | a0001c0002t0003g0080 a0001c0002t0003g0166 a0001c0002t0003g0167 others(4): Show |
7 | HG01123.hp1 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-1217_235-1206d others(14): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | C | CTTTTTTT others(6): Show |
2 | a0001c0002t0003g0170 a0001c0002t0013g0204 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.235-1218_235-1206d others(15): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | C | CTTTTTTT others(7): Show |
1 | a0001c0002t0003g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.235-1219_235-1206d others(16): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | C | CTTTTTTT others(9): Show |
1 | a0001c0002t0003g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.235-1221_235-1206d others(18): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | C | CTTTTTTT others(11): Show |
1 | a0001c0002t0003g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.235-1223_235-1206d others(20): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | C | CTTTTTTT others(14): Show |
1 | a0001c0002t0003g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.235-1226_235-1206d others(23): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | CTTTTTTT others(6): Show |
C | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.235-1218_235-1206d others(15): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | CTTTTTTT others(9): Show |
C | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.235-1221_235-1206d others(18): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | CTTTTTTT others(10): Show |
C | 53 | a0001c0001t0001g0194 a0001c0001t0001g0227 a0001c0001t0002g0010 others(50): Show |
56 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.235-1222_235-1206d others(19): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | CTTTTTTT others(13): Show |
C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0134 a0001c0001t0022g0275 |
3 | HG02738.hp2 HG03704.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.235-1225_235-1206d others(22): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | CTTTTTTT others(14): Show |
C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(172): Show |
180 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.235-1226_235-1206d others(23): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048648 | CTTTTTTT others(15): Show |
C | 1 | a0001c0001t0001g0287 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.235-1227_235-1206d others(24): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108048648 | ||||||
| chr11:108048848 | G | C | 1 | a0001c0001t0001g0146 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.235-1042G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108048848 | |||||||
| chr11:108048901 | G | A | 1 | a0001c0001t0015g0237 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.235-989G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108048901 | |||||||
| chr11:108048908 | G | T | 1 | a0001c0001t0020g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.235-982G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108048908 | |||||||
| chr11:108048940 | C | T | 74 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0078 others(71): Show |
75 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.235-950C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108048940 | |||||||
| chr11:108049247 | GT | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(279): Show |
292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.235-639delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 108049247 | ||||||
| chr11:108049590 | G | A | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.235-300G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108049590 | |||||||
| chr11:108049647 | A | G | 9 | a0001c0002t0002g0054 a0001c0002t0002g0056 a0001c0002t0002g0057 others(6): Show |
9 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-243A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108049647 | |||||||
| chr11:108049689 | C | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-201C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 3/18 | chr11 | 108049689 | |||||||
| chr11:108050075 | A | G | 1 | a0001c0002t0003g0187 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.411+9A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108050075 | |||||||
| chr11:108050405 | C | T | 1 | a0001c0002t0003g0186 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.411+339C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108050405 | |||||||
| chr11:108050484 | A | G | 1 | a0001c0001t0001g0289 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.411+418A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108050484 | |||||||
| chr11:108050680 | A | G | 1 | a0001c0001t0023g0296 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.411+614A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108050680 | |||||||
| chr11:108050991 | T | A | 6 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(3): Show |
6 | HG01081.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+925T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108050991 | |||||||
| chr11:108051010 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.411+944A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108051010 | |||||||
| chr11:108051036 | T | C | 4 | a0001c0002t0004g0199 a0001c0002t0004g0200 a0001c0002t0004g0201 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+970T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108051036 | |||||||
| chr11:108051364 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.412-1296T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108051364 | |||||||
| chr11:108051537 | T | C | 1 | a0001c0001t0021g0190 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.412-1123T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108051537 | |||||||
| chr11:108051563 | T | C | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.412-1097T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108051563 | |||||||
| chr11:108051730 | C | A | 1 | a0001c0002t0002g0003 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.412-930C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108051730 | |||||||
| chr11:108051783 | A | G | 19 | a0001c0001t0001g0194 a0001c0001t0002g0010 a0001c0001t0002g0234 others(16): Show |
20 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.412-877A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108051783 | |||||||
| chr11:108051785 | A | G | 23 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(20): Show |
25 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.412-875A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108051785 | |||||||
| chr11:108051802 | A | G | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.412-858A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108051802 | |||||||
| chr11:108052251 | C | G | 3 | a0001c0001t0001g0188 a0001c0001t0020g0189 a0001c0001t0021g0190 |
3 | HG01243.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.412-409C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108052251 | |||||||
| chr11:108052252 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(279): Show |
292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.412-408A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108052252 | |||||||
| chr11:108052259 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.412-401C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108052259 | |||||||
| chr11:108052339 | G | A | 7 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG00733.hp2 HG00735.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.412-321G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108052339 | |||||||
| chr11:108052503 | C | A | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-157C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 4/18 | chr11 | 108052503 | |||||||
| chr11:108053021 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.553+220T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053021 | |||||||
| chr11:108053031 | G | T | 299 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
309 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.553+230G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053031 | |||||||
| chr11:108053074 | T | C | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.553+273T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053074 | |||||||
| chr11:108053377 | A | G | 7 | a0001c0002t0003g0164 a0001c0002t0003g0174 a0001c0002t0003g0175 others(4): Show |
7 | HG00741.hp2 HG01496.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.553+576A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053377 | |||||||
| chr11:108053449 | C | T | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.553+648C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053449 | |||||||
| chr11:108053538 | C | A | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.553+737C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053538 | |||||||
| chr11:108053675 | A | G | 1 | a0001c0002t0003g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.553+874A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053675 | |||||||
| chr11:108053678 | C | CT | 18 | a0001c0001t0001g0194 a0001c0001t0001g0243 a0001c0001t0002g0010 others(15): Show |
19 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.553+894dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 108053678 | ||||||
| chr11:108053678 | CT | C | 8 | a0001c0001t0001g0228 a0001c0001t0001g0238 a0001c0001t0001g0250 others(5): Show |
8 | HG01074.hp1 HG01081.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.553+894delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 108053678 | ||||||
| chr11:108053705 | G | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.553+904G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053705 | |||||||
| chr11:108053754 | A | G | 52 | a0001c0001t0001g0194 a0001c0001t0001g0227 a0001c0001t0002g0010 others(49): Show |
55 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.554-893A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053754 | |||||||
| chr11:108053831 | A | G | 12 | a0001c0001t0001g0194 a0001c0001t0002g0010 a0001c0001t0002g0234 others(9): Show |
13 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.554-816A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053831 | |||||||
| chr11:108053849 | G | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.554-798G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053849 | |||||||
| chr11:108053873 | G | T | 1 | a0001c0001t0001g0025 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.554-774G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053873 | |||||||
| chr11:108053938 | C | G | 1 | a0001c0004t0012g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.554-709C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108053938 | |||||||
| chr11:108054106 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.554-541G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108054106 | |||||||
| chr11:108054289 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.554-358T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108054289 | |||||||
| chr11:108054505 | G | A | 5 | a0001c0002t0009g0058 a0001c0002t0009g0059 a0001c0002t0009g0060 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.554-142G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108054505 | |||||||
| chr11:108054534 | C | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0113 |
2 | NA18982.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.554-113C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108054534 | |||||||
| chr11:108054576 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
187 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.554-71A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108054576 | |||||||
| chr11:108054600 | C | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.554-47C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 5/18 | chr11 | 108054600 | |||||||
| chr11:108054830 | T | C | 50 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(47): Show |
53 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.699+38T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 6/18 | chr11 | 108054830 | |||||||
| chr11:108055002 | G | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.780+47G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055002 | |||||||
| chr11:108055294 | T | C | 1 | a0001c0002t0003g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.780+339T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055294 | |||||||
| chr11:108055516 | A | G | 1 | a0001c0001t0021g0190 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.780+561A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055516 | |||||||
| chr11:108055529 | G | C | 1 | a0001c0002t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.780+574G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055529 | |||||||
| chr11:108055609 | TAATA | T | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.780+659_780+662del others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108055609 | ||||||
| chr11:108055614 | A | AAT | 10 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(7): Show |
11 | HG01081.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.780+675_780+676dup others(2): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108055614 | ||||||
| chr11:108055614 | AAT | A | 8 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(5): Show |
8 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+675_780+676del others(2): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108055614 | ||||||
| chr11:108055618 | T | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.780+663T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055618 | |||||||
| chr11:108055719 | C | T | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.780+764C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055719 | |||||||
| chr11:108055775 | C | T | 1 | a0001c0001t0014g0219 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.780+820C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055775 | |||||||
| chr11:108055776 | G | T | 1 | a0001c0004t0012g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.780+821G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055776 | |||||||
| chr11:108055805 | A | T | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.780+850A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055805 | |||||||
| chr11:108055926 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.780+971C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055926 | |||||||
| chr11:108055943 | T | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.780+988T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108055943 | |||||||
| chr11:108056018 | A | G | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.780+1063A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108056018 | |||||||
| chr11:108056342 | A | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
186 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.780+1387A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108056342 | |||||||
| chr11:108056384 | A | G | 1 | a0001c0002t0002g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.780+1429A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108056384 | |||||||
| chr11:108056426 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
187 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.780+1471A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108056426 | |||||||
| chr11:108056468 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.780+1513T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108056468 | |||||||
| chr11:108056579 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.780+1624T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108056579 | |||||||
| chr11:108056774 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02055.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+1819T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108056774 | |||||||
| chr11:108056785 | A | G | 3 | a0001c0002t0004g0072 a0001c0002t0004g0073 a0001c0002t0004g0074 |
3 | HG01074.hp1 HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.780+1830A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108056785 | |||||||
| chr11:108057075 | C | T | 5 | a0001c0002t0009g0058 a0001c0002t0009g0059 a0001c0002t0009g0060 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+2120C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108057075 | |||||||
| chr11:108057363 | T | A | 1 | a0001c0002t0002g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.780+2408T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108057363 | |||||||
| chr11:108057480 | G | A | 39 | a0001c0001t0001g0155 a0001c0002t0003g0080 a0001c0002t0003g0087 others(36): Show |
40 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.780+2525G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108057480 | |||||||
| chr11:108057930 | G | C | 1 | a0001c0001t0001g0019 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.780+2975G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108057930 | |||||||
| chr11:108058025 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.780+3070A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108058025 | |||||||
| chr11:108058049 | A | G | 1 | a0001c0001t0015g0237 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.780+3094A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108058049 | |||||||
| chr11:108058166 | G | A | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+3211G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108058166 | |||||||
| chr11:108058187 | C | A | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+3232C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108058187 | |||||||
| chr11:108058208 | C | CA | 16 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(13): Show |
16 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.780+3271dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108058208 | ||||||
| chr11:108058208 | CA | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(137): Show |
145 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.780+3271delA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108058208 | ||||||
| chr11:108058208 | CAA | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(17): Show |
22 | HG00735.hp2 HG01070.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.780+3270_780+3271d others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108058208 | ||||||
| chr11:108058245 | C | CT | 99 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(96): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.780+3311dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108058245 | ||||||
| chr11:108058245 | C | CTT | 35 | a0001c0001t0001g0029 a0001c0001t0001g0078 a0001c0001t0001g0089 others(32): Show |
35 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.780+3310_780+3311d others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108058245 | ||||||
| chr11:108058245 | C | CTTTT | 25 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0163 others(22): Show |
25 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.780+3308_780+3311d others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108058245 | ||||||
| chr11:108058499 | C | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+3544C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108058499 | |||||||
| chr11:108058539 | C | T | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.780+3584C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108058539 | |||||||
| chr11:108058543 | C | T | 3 | a0001c0002t0004g0026 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+3588C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108058543 | |||||||
| chr11:108058666 | G | A | 1 | a0001c0002t0017g0178 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.780+3711G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108058666 | |||||||
| chr11:108058931 | G | A | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.780+3976G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108058931 | |||||||
| chr11:108059036 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
186 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.780+4081A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059036 | |||||||
| chr11:108059072 | G | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.780+4117G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059072 | |||||||
| chr11:108059291 | G | A | 8 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
8 | HG00544.hp2 NA18939.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+4336G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059291 | |||||||
| chr11:108059299 | C | T | 1 | a0001c0002t0017g0178 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.780+4344C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059299 | |||||||
| chr11:108059313 | G | A | 10 | a0001c0002t0002g0051 a0001c0002t0002g0054 a0001c0002t0002g0056 others(7): Show |
10 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.780+4358G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059313 | |||||||
| chr11:108059645 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.780+4690G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059645 | |||||||
| chr11:108059714 | T | A | 1 | a0001c0002t0011g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.780+4759T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059714 | |||||||
| chr11:108059732 | A | C | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.780+4777A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059732 | |||||||
| chr11:108059809 | A | C | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.780+4854A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059809 | |||||||
| chr11:108059814 | G | A | 11 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(8): Show |
12 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+4859G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059814 | |||||||
| chr11:108059871 | G | A | 11 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(8): Show |
12 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+4916G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059871 | |||||||
| chr11:108059882 | TA | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(275): Show |
287 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.780+4943delA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108059882 | ||||||
| chr11:108059940 | T | C | 282 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(279): Show |
292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.780+4985T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059940 | |||||||
| chr11:108059942 | T | A | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.780+4987T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059942 | |||||||
| chr11:108059979 | G | A | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.780+5024G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108059979 | |||||||
| chr11:108060089 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA18946.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.780+5134A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060089 | |||||||
| chr11:108060111 | A | C | 5 | a0001c0002t0009g0058 a0001c0002t0009g0059 a0001c0002t0009g0060 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+5156A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060111 | |||||||
| chr11:108060202 | A | C | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.780+5247A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060202 | |||||||
| chr11:108060229 | G | A | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+5274G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060229 | |||||||
| chr11:108060244 | T | C | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.780+5289T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060244 | |||||||
| chr11:108060252 | C | T | 1 | a0001c0002t0002g0212 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.780+5297C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060252 | |||||||
| chr11:108060336 | G | A | 22 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(19): Show |
24 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.780+5381G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060336 | |||||||
| chr11:108060392 | A | G | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.780+5437A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060392 | |||||||
| chr11:108060523 | T | G | 1 | a0001c0002t0029g0068 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.780+5568T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060523 | |||||||
| chr11:108060626 | A | C | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.780+5671A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060626 | |||||||
| chr11:108060729 | C | T | 36 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(33): Show |
37 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.780+5774C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060729 | |||||||
| chr11:108060828 | C | CA | 10 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(7): Show |
11 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.780+5884dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108060828 | ||||||
| chr11:108060841 | A | C | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.780+5886A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108060841 | |||||||
| chr11:108061201 | T | A | 1 | a0001c0001t0001g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.780+6246T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108061201 | |||||||
| chr11:108061434 | A | C | 4 | a0001c0002t0004g0199 a0001c0002t0004g0200 a0001c0002t0004g0201 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+6479A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108061434 | |||||||
| chr11:108061495 | A | G | 52 | a0001c0001t0001g0194 a0001c0001t0002g0010 a0001c0001t0002g0234 others(49): Show |
55 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.780+6540A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108061495 | |||||||
| chr11:108061527 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.780+6572C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108061527 | |||||||
| chr11:108061665 | T | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(93): Show |
100 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.780+6710T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108061665 | |||||||
| chr11:108061687 | A | G | 1 | a0001c0002t0002g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.780+6732A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108061687 | |||||||
| chr11:108061816 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.780+6861A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108061816 | |||||||
| chr11:108061894 | G | GGA | 10 | a0001c0001t0001g0188 a0001c0001t0001g0213 a0001c0001t0001g0214 others(7): Show |
11 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.780+6960_780+6961d others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108061894 | ||||||
| chr11:108061894 | GGAGAGA | G | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.780+6956_780+6961d others(8): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108061894 | ||||||
| chr11:108061999 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
187 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.780+7044T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108061999 | |||||||
| chr11:108062006 | A | G | 2 | a0001c0001t0001g0194 a0001c0001t0002g0255 |
2 | HG01243.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.780+7051A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062006 | |||||||
| chr11:108062052 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0102 a0001c0001t0001g0105 |
3 | HG02135.hp1 NA18974.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.780+7097C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062052 | |||||||
| chr11:108062221 | C | CT | 52 | a0001c0001t0001g0194 a0001c0001t0002g0010 a0001c0001t0002g0234 others(49): Show |
55 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.780+7267dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108062221 | ||||||
| chr11:108062236 | C | T | 1 | a0001c0002t0003g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.780+7281C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062236 | |||||||
| chr11:108062275 | G | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+7320G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062275 | |||||||
| chr11:108062276 | G | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+7321G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062276 | |||||||
| chr11:108062284 | T | G | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.780+7329T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062284 | |||||||
| chr11:108062360 | C | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
184 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.780+7405C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062360 | |||||||
| chr11:108062367 | G | A | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+7412G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062367 | |||||||
| chr11:108062729 | A | G | 1 | a0001c0002t0032g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.781-7367A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062729 | |||||||
| chr11:108062748 | T | C | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-7348T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062748 | |||||||
| chr11:108062906 | C | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 |
3 | HG00738.hp1 HG01099.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.781-7190C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108062906 | |||||||
| chr11:108063118 | T | C | 10 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(7): Show |
10 | HG00544.hp2 HG00673.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.781-6978T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063118 | |||||||
| chr11:108063175 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.781-6921C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063175 | |||||||
| chr11:108063250 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.781-6846A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063250 | |||||||
| chr11:108063286 | G | A | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.781-6810G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063286 | |||||||
| chr11:108063614 | T | C | 1 | a0001c0002t0003g0176 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.781-6482T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063614 | |||||||
| chr11:108063656 | T | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
267 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.781-6440T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063656 | |||||||
| chr11:108063657 | A | AAAAT | 25 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(22): Show |
27 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.781-6436_781-6435i others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108063657 | ||||||
| chr11:108063661 | A | AAAAAT | 45 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(42): Show |
46 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.781-6432_781-6431i others(7): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108063661 | ||||||
| chr11:108063661 | A | AAAAT | 33 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(30): Show |
35 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.781-6425_781-6422d others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108063661 | ||||||
| chr11:108063661 | A | AAAT | 180 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
185 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.781-6433_781-6432i others(5): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108063661 | ||||||
| chr11:108063661 | A | T | 26 | a0001c0001t0001g0121 a0001c0002t0002g0003 a0001c0002t0002g0033 others(23): Show |
28 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.781-6435A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063661 | |||||||
| chr11:108063688 | C | T | 2 | a0001c0001t0001g0025 a0001c0002t0010g0162 |
2 | HG03471.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.781-6408C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063688 | |||||||
| chr11:108063841 | C | T | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.781-6255C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063841 | |||||||
| chr11:108063860 | C | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
187 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.781-6236C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063860 | |||||||
| chr11:108063937 | A | G | 3 | a0001c0002t0002g0003 a0001c0002t0002g0041 a0001c0002t0002g0065 |
4 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-6159A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108063937 | |||||||
| chr11:108064004 | A | G | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.781-6092A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108064004 | |||||||
| chr11:108064006 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.781-6090T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108064006 | |||||||
| chr11:108064157 | C | T | 3 | a0001c0003t0005g0001 a0001c0003t0005g0011 a0001c0003t0005g0012 |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-5939C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108064157 | |||||||
| chr11:108064158 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.781-5938G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108064158 | |||||||
| chr11:108064426 | G | T | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.781-5670G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108064426 | |||||||
| chr11:108064457 | C | T | 3 | a0001c0002t0002g0003 a0001c0002t0002g0041 a0001c0002t0002g0065 |
4 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-5639C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108064457 | |||||||
| chr11:108064566 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0023g0296 |
2 | HG01175.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.781-5530C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108064566 | |||||||
| chr11:108064571 | G | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-5525G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108064571 | |||||||
| chr11:108064987 | T | C | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.781-5109T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108064987 | |||||||
| chr11:108065060 | C | T | 1 | a0001c0002t0004g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.781-5036C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108065060 | |||||||
| chr11:108065150 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.781-4946C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108065150 | |||||||
| chr11:108065372 | A | G | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.781-4724A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108065372 | |||||||
| chr11:108065446 | C | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | NA18966.hp1 NA19056.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.781-4650C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108065446 | |||||||
| chr11:108065447 | G | A | 8 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-4649G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108065447 | |||||||
| chr11:108065551 | C | T | 1 | a0001c0001t0021g0190 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.781-4545C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108065551 | |||||||
| chr11:108065586 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.781-4510G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108065586 | |||||||
| chr11:108065593 | A | G | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.781-4503A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108065593 | |||||||
| chr11:108065852 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0250 |
2 | NA19003.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.781-4244G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108065852 | |||||||
| chr11:108066157 | G | A | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-3939G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066157 | |||||||
| chr11:108066157 | G | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0098 a0001c0001t0001g0099 others(40): Show |
44 | HG00408.hp1 HG00438.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.781-3939G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066157 | |||||||
| chr11:108066238 | G | T | 1 | a0001c0002t0013g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.781-3858G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066238 | |||||||
| chr11:108066249 | G | A | 11 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(8): Show |
12 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-3847G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066249 | |||||||
| chr11:108066353 | A | G | 1 | a0001c0002t0025g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781-3743A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066353 | |||||||
| chr11:108066461 | A | G | 1 | a0001c0002t0002g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.781-3635A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066461 | |||||||
| chr11:108066468 | A | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.781-3628A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066468 | |||||||
| chr11:108066584 | A | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.781-3512A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066584 | |||||||
| chr11:108066599 | C | G | 1 | a0001c0001t0001g0251 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.781-3497C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066599 | |||||||
| chr11:108066653 | A | G | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-3443A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066653 | |||||||
| chr11:108066655 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.781-3441T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066655 | |||||||
| chr11:108066797 | G | C | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-3299G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066797 | |||||||
| chr11:108066872 | T | A | 2 | a0001c0001t0001g0110 a0001c0001t0019g0097 |
2 | NA18955.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.781-3224T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066872 | |||||||
| chr11:108066902 | A | T | 1 | a0001c0002t0002g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.781-3194A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066902 | |||||||
| chr11:108066935 | A | T | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.781-3161A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108066935 | |||||||
| chr11:108067012 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.781-3084T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067012 | |||||||
| chr11:108067159 | A | C | 1 | a0001c0001t0010g0144 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.781-2937A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067159 | |||||||
| chr11:108067358 | T | C | 4 | a0001c0002t0004g0199 a0001c0002t0004g0200 a0001c0002t0004g0201 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-2738T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067358 | |||||||
| chr11:108067360 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.781-2736A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067360 | |||||||
| chr11:108067453 | A | G | 27 | a0001c0001t0001g0019 a0001c0001t0001g0078 a0001c0001t0001g0089 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.781-2643A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067453 | |||||||
| chr11:108067474 | TATGAA | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
182 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.781-2619_781-2615d others(7): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108067474 | ||||||
| chr11:108067749 | A | G | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.781-2347A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067749 | |||||||
| chr11:108067790 | T | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(215): Show |
224 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.781-2306T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067790 | |||||||
| chr11:108067851 | G | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(217): Show |
226 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.781-2245G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067851 | |||||||
| chr11:108067903 | A | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 |
3 | HG00738.hp1 HG01099.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.781-2193A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067903 | |||||||
| chr11:108067954 | G | A | 1 | a0001c0001t0026g0103 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.781-2142G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067954 | |||||||
| chr11:108067992 | G | C | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.781-2104G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108067992 | |||||||
| chr11:108068004 | C | T | 31 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(28): Show |
31 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.781-2092C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068004 | |||||||
| chr11:108068007 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.781-2089C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068007 | |||||||
| chr11:108068012 | T | C | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-2084T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068012 | |||||||
| chr11:108068028 | A | G | 1 | a0001c0001t0006g0266 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.781-2068A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068028 | |||||||
| chr11:108068090 | T | C | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.781-2006T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068090 | |||||||
| chr11:108068159 | C | T | 3 | a0001c0002t0002g0003 a0001c0002t0002g0041 a0001c0002t0002g0065 |
4 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-1937C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068159 | |||||||
| chr11:108068237 | G | C | 1 | a0001c0002t0002g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.781-1859G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068237 | |||||||
| chr11:108068314 | T | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
5 | HG01168.hp1 HG01192.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-1782T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068314 | |||||||
| chr11:108068314 | T | TTTTTG | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-1760_781-1756d others(7): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 108068314 | ||||||
| chr11:108068441 | C | A | 55 | a0001c0001t0001g0194 a0001c0001t0002g0010 a0001c0001t0002g0234 others(52): Show |
59 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.781-1655C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068441 | |||||||
| chr11:108068476 | G | T | 1 | a0001c0002t0003g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.781-1620G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068476 | |||||||
| chr11:108068515 | A | G | 52 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(49): Show |
55 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.781-1581A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068515 | |||||||
| chr11:108068868 | A | G | 2 | a0001c0002t0003g0183 a0001c0002t0003g0184 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.781-1228A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068868 | |||||||
| chr11:108068881 | T | A | 1 | a0001c0001t0006g0266 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.781-1215T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068881 | |||||||
| chr11:108068900 | A | G | 31 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(28): Show |
31 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.781-1196A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068900 | |||||||
| chr11:108068934 | G | A | 2 | a0001c0002t0004g0201 a0001c0002t0004g0300 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.781-1162G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108068934 | |||||||
| chr11:108069037 | G | T | 281 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
291 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.781-1059G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108069037 | |||||||
| chr11:108069136 | A | G | 1 | a0001c0002t0029g0068 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.781-960A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108069136 | |||||||
| chr11:108069315 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
186 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.781-781A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108069315 | |||||||
| chr11:108069376 | G | A | 1 | a0001c0001t0006g0266 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.781-720G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108069376 | |||||||
| chr11:108069523 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0001g0239 a0001c0001t0001g0295 |
3 | NA18947.hp2 NA19055.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.781-573A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108069523 | |||||||
| chr11:108069714 | G | A | 31 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(28): Show |
31 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.781-382G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108069714 | |||||||
| chr11:108069811 | G | A | 1 | a0001c0002t0025g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781-285G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108069811 | |||||||
| chr11:108069819 | A | G | 4 | a0001c0001t0001g0139 a0001c0001t0015g0237 a0001c0001t0015g0245 others(1): Show |
4 | HG00738.hp2 HG01261.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-277A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108069819 | |||||||
| chr11:108069847 | C | A | 1 | a0001c0002t0002g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.781-249C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108069847 | |||||||
| chr11:108069965 | G | C | 1 | a0001c0002t0001g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.781-131G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 7/18 | chr11 | 108069965 | |||||||
| chr11:108070267 | T | C | 1 | a0001c0006t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.874+78T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108070267 | |||||||
| chr11:108070435 | C | G | 1 | a0001c0001t0010g0224 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.874+246C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108070435 | |||||||
| chr11:108070476 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
183 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.874+287G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108070476 | |||||||
| chr11:108070554 | G | A | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.874+365G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108070554 | |||||||
| chr11:108070624 | A | AT | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.874+442dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 108070624 | ||||||
| chr11:108070752 | C | T | 1 | a0001c0002t0003g0170 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.874+563C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108070752 | |||||||
| chr11:108070770 | C | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.874+581C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108070770 | |||||||
| chr11:108070943 | G | T | 1 | a0001c0002t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.874+754G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108070943 | |||||||
| chr11:108071026 | G | C | 1 | a0001c0002t0009g0058 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.874+837G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071026 | |||||||
| chr11:108071178 | G | A | 3 | a0001c0002t0013g0202 a0001c0002t0013g0203 a0001c0002t0013g0204 |
3 | HG02258.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.874+989G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071178 | |||||||
| chr11:108071249 | C | T | 283 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(280): Show |
293 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.874+1060C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071249 | |||||||
| chr11:108071324 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
182 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.875-1008G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071324 | |||||||
| chr11:108071334 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0020g0189 a0001c0001t0021g0190 |
3 | HG01243.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.875-998C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071334 | |||||||
| chr11:108071407 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
5 | HG01168.hp1 HG01192.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.875-925C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071407 | |||||||
| chr11:108071468 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.875-864G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071468 | |||||||
| chr11:108071528 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.875-804G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071528 | |||||||
| chr11:108071574 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.875-758G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071574 | |||||||
| chr11:108071774 | T | C | 5 | a0001c0002t0004g0198 a0001c0002t0011g0197 a0001c0002t0013g0202 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.875-558T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071774 | |||||||
| chr11:108071848 | C | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.875-484C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071848 | |||||||
| chr11:108071934 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.875-398T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071934 | |||||||
| chr11:108071988 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.875-344G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108071988 | |||||||
| chr11:108072100 | G | A | 11 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(8): Show |
12 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.875-232G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108072100 | |||||||
| chr11:108072128 | G | A | 2 | a0001c0002t0004g0201 a0001c0002t0004g0300 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.875-204G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 8/18 | chr11 | 108072128 | |||||||
| chr11:108072533 | TAGTG | T | 29 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(26): Show |
30 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1005+74_1005+77del others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr11 | 108072533 | ||||||
| chr11:108072541 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1005+79G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 9/18 | chr11 | 108072541 | |||||||
| chr11:108072780 | A | G | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1005+318A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 9/18 | chr11 | 108072780 | |||||||
| chr11:108072868 | A | G | 3 | a0001c0003t0005g0001 a0001c0003t0005g0011 a0001c0003t0005g0012 |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+406A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 9/18 | chr11 | 108072868 | |||||||
| chr11:108072968 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02055.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006-422C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 9/18 | chr11 | 108072968 | |||||||
| chr11:108073183 | C | T | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.1006-207C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 9/18 | chr11 | 108073183 | |||||||
| chr11:108073349 | T | C | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1006-41T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 9/18 | chr11 | 108073349 | |||||||
| chr11:108073513 | T | C | 1 | a0001c0002t0011g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1113+16T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108073513 | |||||||
| chr11:108073618 | T | C | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1113+121T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108073618 | |||||||
| chr11:108073966 | C | A | 5 | a0001c0002t0004g0198 a0001c0002t0011g0197 a0001c0002t0013g0202 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+469C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108073966 | |||||||
| chr11:108074190 | A | AT | 53 | a0001c0001t0001g0030 a0001c0001t0001g0134 a0001c0001t0023g0296 others(50): Show |
54 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1113+714dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr11 | 108074190 | ||||||
| chr11:108074190 | AT | A | 15 | a0001c0001t0001g0091 a0001c0001t0001g0130 a0001c0001t0001g0153 others(12): Show |
15 | HG01099.hp2 HG01884.hp1 HG02897.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+714delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr11 | 108074190 | ||||||
| chr11:108074224 | C | T | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1113+727C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074224 | |||||||
| chr11:108074237 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1113+740C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074237 | |||||||
| chr11:108074275 | A | C | 2 | a0001c0006t0001g0115 a0001c0006t0001g0116 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1113+778A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074275 | |||||||
| chr11:108074297 | C | T | 1 | a0001c0002t0003g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1113+800C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074297 | |||||||
| chr11:108074370 | T | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
186 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.1113+873T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074370 | |||||||
| chr11:108074377 | T | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1113+880T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074377 | |||||||
| chr11:108074531 | G | T | 1 | a0001c0002t0001g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1113+1034G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074531 | |||||||
| chr11:108074569 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
186 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.1113+1072C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074569 | |||||||
| chr11:108074581 | G | A | 4 | a0001c0001t0006g0008 a0001c0001t0006g0248 a0001c0001t0006g0266 others(1): Show |
5 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+1084G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074581 | |||||||
| chr11:108074680 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1113+1183C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074680 | |||||||
| chr11:108074695 | A | G | 3 | a0001c0002t0013g0202 a0001c0002t0013g0203 a0001c0002t0013g0204 |
3 | HG02258.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1113+1198A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074695 | |||||||
| chr11:108074747 | G | T | 2 | a0001c0002t0004g0026 a0001c0002t0025g0027 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1113+1250G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074747 | |||||||
| chr11:108074885 | G | A | 8 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+1388G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108074885 | |||||||
| chr11:108075117 | T | C | 2 | a0001c0002t0004g0026 a0001c0002t0025g0027 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1113+1620T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075117 | |||||||
| chr11:108075211 | C | G | 1 | a0001c0002t0004g0205 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1113+1714C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075211 | |||||||
| chr11:108075244 | G | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(216): Show |
225 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.1113+1747G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075244 | |||||||
| chr11:108075249 | G | T | 31 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(28): Show |
31 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.1113+1752G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075249 | |||||||
| chr11:108075282 | T | G | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1113+1785T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075282 | |||||||
| chr11:108075366 | T | C | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1113+1869T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075366 | |||||||
| chr11:108075546 | A | G | 1 | a0001c0001t0022g0275 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1113+2049A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075546 | |||||||
| chr11:108075554 | G | T | 1 | a0001c0002t0005g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1113+2057G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075554 | |||||||
| chr11:108075634 | C | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG00738.hp1 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+2137C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075634 | |||||||
| chr11:108075647 | C | T | 1 | a0001c0002t0011g0165 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1113+2150C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075647 | |||||||
| chr11:108075675 | G | A | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.1113+2178G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075675 | |||||||
| chr11:108075720 | A | G | 297 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(294): Show |
307 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.1113+2223A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075720 | |||||||
| chr11:108075728 | A | C | 7 | a0001c0002t0003g0164 a0001c0002t0003g0174 a0001c0002t0003g0175 others(4): Show |
7 | HG00741.hp2 HG01496.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+2231A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075728 | |||||||
| chr11:108075926 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG00408.hp2 NA18972.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1114-2250A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075926 | |||||||
| chr11:108075997 | A | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02055.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1114-2179A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108075997 | |||||||
| chr11:108076314 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1114-1862A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108076314 | |||||||
| chr11:108076324 | A | G | 1 | a0001c0002t0001g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1114-1852A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108076324 | |||||||
| chr11:108076332 | C | T | 11 | a0001c0002t0002g0051 a0001c0002t0002g0054 a0001c0002t0002g0056 others(8): Show |
11 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.1114-1844C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108076332 | |||||||
| chr11:108076472 | T | G | 1 | a0001c0001t0001g0269 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1114-1704T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108076472 | |||||||
| chr11:108076570 | G | T | 52 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(49): Show |
55 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1114-1606G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108076570 | |||||||
| chr11:108076623 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1114-1553A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108076623 | |||||||
| chr11:108076730 | G | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(81): Show |
85 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1114-1446G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108076730 | |||||||
| chr11:108076755 | T | G | 2 | a0001c0005t0016g0066 a0001c0005t0016g0067 |
2 | NA18970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1114-1421T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108076755 | |||||||
| chr11:108076891 | A | G | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-1285A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108076891 | |||||||
| chr11:108077030 | T | C | 23 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(20): Show |
25 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1114-1146T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077030 | |||||||
| chr11:108077032 | T | C | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-1144T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077032 | |||||||
| chr11:108077036 | T | C | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114-1140T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077036 | |||||||
| chr11:108077041 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1114-1135G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077041 | |||||||
| chr11:108077101 | T | C | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-1075T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077101 | |||||||
| chr11:108077270 | C | A | 3 | a0001c0002t0003g0087 a0001c0002t0003g0088 a0001c0002t0003g0176 |
3 | HG02602.hp2 HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1114-906C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077270 | |||||||
| chr11:108077423 | A | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0102 a0001c0001t0001g0105 |
3 | HG02135.hp1 NA18974.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1114-753A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077423 | |||||||
| chr11:108077460 | T | A | 39 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(36): Show |
40 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.1114-716T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077460 | |||||||
| chr11:108077612 | C | CAA | 217 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
223 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1114-564_1114-563i others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077612 | |||||||
| chr11:108077630 | C | CA | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
183 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1114-533dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr11 | 108077630 | ||||||
| chr11:108077831 | G | A | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114-345G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077831 | |||||||
| chr11:108077852 | G | A | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1114-324G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108077852 | |||||||
| chr11:108078054 | G | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1114-122G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108078054 | |||||||
| chr11:108078110 | A | G | 4 | a0001c0002t0004g0199 a0001c0002t0004g0200 a0001c0002t0004g0201 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-66A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108078110 | |||||||
| chr11:108078131 | T | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(87): Show |
94 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1114-45T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 10/18 | chr11 | 108078131 | |||||||
| chr11:108078352 | T | C | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1178+112T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108078352 | |||||||
| chr11:108078398 | TATTAA | T | 18 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0035 others(15): Show |
20 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1178+163_1178+167d others(7): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108078398 | ||||||
| chr11:108078443 | T | TA | 18 | a0001c0001t0001g0194 a0001c0001t0002g0010 a0001c0001t0002g0234 others(15): Show |
19 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1178+213dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108078443 | ||||||
| chr11:108078659 | A | G | 9 | a0001c0002t0002g0054 a0001c0002t0002g0056 a0001c0002t0002g0057 others(6): Show |
9 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.1178+419A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108078659 | |||||||
| chr11:108078734 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(279): Show |
292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.1178+494A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108078734 | |||||||
| chr11:108078761 | C | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1178+521C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108078761 | |||||||
| chr11:108078964 | A | T | 1 | a0001c0001t0020g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1178+724A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108078964 | |||||||
| chr11:108079057 | ATCT | A | 3 | a0001c0002t0010g0162 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1178+824_1178+826d others(5): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108079057 | ||||||
| chr11:108079077 | A | G | 1 | a0001c0002t0025g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1178+837A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079077 | |||||||
| chr11:108079347 | C | T | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1178+1107C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079347 | |||||||
| chr11:108079348 | C | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1178+1108C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079348 | |||||||
| chr11:108079473 | T | C | 1 | a0001c0001t0020g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1178+1233T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079473 | |||||||
| chr11:108079567 | G | T | 5 | a0001c0002t0009g0058 a0001c0002t0009g0059 a0001c0002t0009g0060 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1178+1327G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079567 | |||||||
| chr11:108079589 | T | G | 1 | a0001c0001t0022g0275 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1178+1349T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079589 | |||||||
| chr11:108079597 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1178+1357A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079597 | |||||||
| chr11:108079649 | A | G | 1 | a0001c0001t0022g0275 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1178+1409A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079649 | |||||||
| chr11:108079659 | G | T | 74 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0078 others(71): Show |
75 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1178+1419G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079659 | |||||||
| chr11:108079704 | A | G | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1178+1464A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079704 | |||||||
| chr11:108079740 | C | T | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.1178+1500C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079740 | |||||||
| chr11:108079870 | TTTCA | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
6 | HG00280.hp2 NA18946.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1178+1634_1178+163 others(8): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108079870 | ||||||
| chr11:108079880 | C | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1178+1640C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108079880 | |||||||
| chr11:108080007 | G | GTTTAGTG others(3): Show |
2 | a0001c0002t0003g0087 a0001c0002t0003g0088 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1178+1771_1178+178 others(14): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108080007 | ||||||
| chr11:108080075 | C | T | 1 | a0001c0002t0002g0036 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1178+1835C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108080075 | |||||||
| chr11:108080099 | G | A | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1178+1859G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108080099 | |||||||
| chr11:108080111 | CT | C | 70 | a0001c0001t0001g0099 a0001c0001t0001g0140 a0001c0001t0001g0214 others(67): Show |
74 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1178+1887delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108080111 | ||||||
| chr11:108080127 | T | TC | 3 | a0001c0001t0001g0232 a0001c0001t0001g0292 a0001c0001t0010g0224 |
3 | HG01175.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1178+1889dupC | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108080127 | ||||||
| chr11:108080127 | T | TTC | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(85): Show |
92 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1178+1887_1178+188 others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108080127 | |||||||
| chr11:108080253 | T | C | 8 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+2013T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108080253 | |||||||
| chr11:108080290 | C | T | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.1178+2050C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108080290 | |||||||
| chr11:108080354 | G | A | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+2114G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108080354 | |||||||
| chr11:108080758 | T | G | 1 | a0001c0001t0001g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1178+2518T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108080758 | |||||||
| chr11:108080785 | T | A | 5 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0095 others(2): Show |
5 | NA18951.hp2 NA18970.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1178+2545T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108080785 | |||||||
| chr11:108080953 | A | ATTAT | 18 | a0001c0002t0002g0034 a0001c0002t0002g0051 a0001c0002t0002g0054 others(15): Show |
18 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1178+2748_1178+275 others(8): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108080953 | ||||||
| chr11:108080953 | ATTAT | A | 47 | a0001c0001t0001g0188 a0001c0001t0020g0189 a0001c0001t0021g0190 others(44): Show |
47 | HG00741.hp2 HG01099.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1178+2748_1178+275 others(8): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108080953 | ||||||
| chr11:108080953 | ATTATTTA others(1): Show |
A | 87 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(84): Show |
88 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1178+2744_1178+275 others(12): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108080953 | ||||||
| chr11:108080953 | ATTATTTA others(5): Show |
A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(87): Show |
94 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1178+2740_1178+275 others(16): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108080953 | ||||||
| chr11:108080953 | ATTATTTA others(9): Show |
A | 1 | a0001c0001t0001g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1178+2736_1178+275 others(20): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108080953 | ||||||
| chr11:108080953 | ATTATTTA others(13): Show |
A | 1 | a0001c0001t0001g0292 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1178+2732_1178+275 others(24): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108080953 | ||||||
| chr11:108081054 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1178+2814A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081054 | |||||||
| chr11:108081152 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1178+2912G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081152 | |||||||
| chr11:108081220 | G | A | 31 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(28): Show |
31 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.1178+2980G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081220 | |||||||
| chr11:108081243 | G | A | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG00738.hp1 HG01099.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+3003G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081243 | |||||||
| chr11:108081479 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1178+3239G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081479 | |||||||
| chr11:108081701 | G | A | 2 | a0001c0002t0027g0217 a0001c0002t0032g0062 |
2 | HG01109.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1178+3461G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081701 | |||||||
| chr11:108081742 | T | C | 1 | a0001c0001t0021g0190 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1178+3502T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081742 | |||||||
| chr11:108081762 | T | A | 1 | a0001c0002t0003g0181 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1178+3522T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081762 | |||||||
| chr11:108081850 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1178+3610G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081850 | |||||||
| chr11:108081890 | A | G | 2 | a0001c0002t0004g0071 a0001c0002t0004g0077 |
2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1178+3650A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081890 | |||||||
| chr11:108081899 | C | G | 3 | a0001c0001t0001g0188 a0001c0001t0020g0189 a0001c0001t0021g0190 |
3 | HG01243.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1178+3659C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108081899 | |||||||
| chr11:108082286 | G | GT | 32 | a0001c0001t0006g0266 a0001c0002t0003g0080 a0001c0002t0003g0087 others(29): Show |
32 | HG00741.hp2 HG01123.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1178+4059dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108082286 | ||||||
| chr11:108082308 | G | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(3): Show |
7 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1178+4068G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108082308 | |||||||
| chr11:108082360 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1178+4120A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108082360 | |||||||
| chr11:108082657 | T | C | 1 | a0001c0002t0004g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1178+4417T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108082657 | |||||||
| chr11:108082660 | T | C | 5 | a0001c0002t0004g0072 a0001c0002t0004g0073 a0001c0002t0004g0074 others(2): Show |
5 | HG01074.hp1 HG02630.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1178+4420T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108082660 | |||||||
| chr11:108082783 | C | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1178+4543C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108082783 | |||||||
| chr11:108082799 | AT | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.1178+4570delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108082799 | ||||||
| chr11:108082830 | T | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.1178+4590T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108082830 | |||||||
| chr11:108082905 | G | A | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+4665G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108082905 | |||||||
| chr11:108083023 | G | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0105 |
2 | NA18974.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1178+4783G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108083023 | |||||||
| chr11:108083165 | T | C | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1178+4925T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108083165 | |||||||
| chr11:108083284 | T | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
186 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.1178+5044T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108083284 | |||||||
| chr11:108083401 | C | T | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.1179-5126C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108083401 | |||||||
| chr11:108083420 | A | G | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179-5107A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108083420 | |||||||
| chr11:108083814 | T | C | 3 | a0001c0001t0001g0188 a0001c0001t0020g0189 a0001c0001t0021g0190 |
3 | HG01243.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1179-4713T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108083814 | |||||||
| chr11:108084218 | T | G | 1 | a0001c0002t0002g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1179-4309T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108084218 | |||||||
| chr11:108084308 | C | T | 1 | a0001c0002t0017g0178 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1179-4219C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108084308 | |||||||
| chr11:108084445 | C | T | 2 | a0001c0001t0020g0189 a0001c0001t0021g0190 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1179-4082C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108084445 | |||||||
| chr11:108084512 | G | T | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1179-4015G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108084512 | |||||||
| chr11:108084529 | T | G | 1 | a0001c0002t0031g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1179-3998T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108084529 | |||||||
| chr11:108084578 | GTTCTTGT others(4): Show |
G | 1 | a0001c0002t0003g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1179-3943_1179-393 others(15): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108084578 | ||||||
| chr11:108084735 | T | C | 3 | a0001c0001t0001g0188 a0001c0001t0020g0189 a0001c0001t0021g0190 |
3 | HG01243.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1179-3792T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108084735 | |||||||
| chr11:108084806 | G | A | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1179-3721G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108084806 | |||||||
| chr11:108084820 | G | A | 1 | a0001c0002t0004g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1179-3707G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108084820 | |||||||
| chr11:108085216 | G | A | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1179-3311G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085216 | |||||||
| chr11:108085334 | A | G | 6 | a0001c0001t0001g0126 a0001c0001t0001g0146 a0001c0001t0001g0148 others(3): Show |
6 | HG00438.hp2 NA18946.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179-3193A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085334 | |||||||
| chr11:108085350 | T | C | 22 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0034 others(19): Show |
24 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1179-3177T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085350 | |||||||
| chr11:108085424 | A | G | 1 | a0001c0002t0005g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1179-3103A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085424 | |||||||
| chr11:108085427 | G | A | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG00738.hp1 HG01099.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1179-3100G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085427 | |||||||
| chr11:108085471 | T | C | 1 | a0001c0002t0032g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1179-3056T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085471 | |||||||
| chr11:108085504 | G | A | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1179-3023G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085504 | |||||||
| chr11:108085581 | T | A | 71 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0078 others(68): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1179-2946T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085581 | |||||||
| chr11:108085628 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1179-2899T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085628 | |||||||
| chr11:108085888 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1179-2639G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085888 | |||||||
| chr11:108085988 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1179-2539G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108085988 | |||||||
| chr11:108086044 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(45): Show |
50 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1179-2483T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108086044 | |||||||
| chr11:108086059 | T | C | 1 | a0002c0008t0001g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1179-2468T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108086059 | |||||||
| chr11:108086076 | A | T | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1179-2451A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108086076 | |||||||
| chr11:108086087 | T | C | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1179-2440T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108086087 | |||||||
| chr11:108086662 | T | C | 31 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(28): Show |
31 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.1179-1865T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108086662 | |||||||
| chr11:108086698 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1179-1829T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108086698 | |||||||
| chr11:108086750 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(94): Show |
101 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1179-1777T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108086750 | |||||||
| chr11:108086867 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1179-1660A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108086867 | |||||||
| chr11:108086960 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1179-1567T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108086960 | |||||||
| chr11:108087181 | C | T | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1179-1346C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108087181 | |||||||
| chr11:108087247 | T | A | 2 | a0001c0006t0001g0115 a0001c0006t0001g0116 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1179-1280T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108087247 | |||||||
| chr11:108087403 | C | G | 3 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 |
3 | HG01081.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1179-1124C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108087403 | |||||||
| chr11:108087446 | A | C | 1 | a0001c0001t0001g0024 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1179-1081A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108087446 | |||||||
| chr11:108087527 | G | A | 1 | a0001c0002t0003g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1179-1000G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108087527 | |||||||
| chr11:108087653 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1179-874A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108087653 | |||||||
| chr11:108087770 | G | GC | 8 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1179-755dupC | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 108087770 | ||||||
| chr11:108087822 | G | A | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179-705G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108087822 | |||||||
| chr11:108087875 | G | C | 1 | a0001c0002t0001g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1179-652G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108087875 | |||||||
| chr11:108087889 | C | T | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1179-638C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108087889 | |||||||
| chr11:108088005 | G | C | 1 | a0001c0002t0007g0050 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1179-522G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108088005 | |||||||
| chr11:108088146 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1179-381A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108088146 | |||||||
| chr11:108088242 | A | G | 4 | a0001c0002t0004g0199 a0001c0002t0004g0200 a0001c0002t0004g0201 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179-285A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108088242 | |||||||
| chr11:108088350 | C | T | 1 | a0001c0002t0002g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1179-177C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 11/18 | chr11 | 108088350 | |||||||
| chr11:108088758 | A | G | 1 | a0001c0002t0003g0167 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1311+99A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 12/18 | chr11 | 108088758 | |||||||
| chr11:108088807 | C | T | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1311+148C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 12/18 | chr11 | 108088807 | |||||||
| chr11:108088808 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1311+149G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 12/18 | chr11 | 108088808 | |||||||
| chr11:108088822 | C | G | 1 | a0001c0001t0001g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1311+163C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 12/18 | chr11 | 108088822 | |||||||
| chr11:108089038 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1311+379T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 12/18 | chr11 | 108089038 | |||||||
| chr11:108089065 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1311+406T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 12/18 | chr11 | 108089065 | |||||||
| chr11:108089110 | A | G | 2 | a0001c0004t0012g0005 a0001c0004t0012g0082 |
3 | HG02572.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1312-382A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 12/18 | chr11 | 108089110 | |||||||
| chr11:108089119 | T | A | 2 | a0001c0006t0001g0115 a0001c0006t0001g0116 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1312-373T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 12/18 | chr11 | 108089119 | |||||||
| chr11:108089181 | ATAAGTAG others(53): Show |
A | 1 | a0001c0002t0001g0083 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1312-310_1312-251d others(62): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 12/18 | chr11 | 108089181 | |||||||
| chr11:108089235 | A | T | 1 | a0001c0002t0003g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1312-257A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 12/18 | chr11 | 108089235 | |||||||
| chr11:108089752 | CAGTT | C | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1443+132_1443+135d others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108089752 | ||||||
| chr11:108089947 | A | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
309 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.1443+324A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108089947 | |||||||
| chr11:108090039 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1443+416C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108090039 | |||||||
| chr11:108090039 | C | CA | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
215 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.1443+426dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108090039 | ||||||
| chr11:108090285 | G | A | 1 | a0001c0001t0020g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1443+662G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108090285 | |||||||
| chr11:108090523 | A | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0235 a0001c0001t0001g0240 |
3 | HG00438.hp1 HG00673.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1443+900A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108090523 | |||||||
| chr11:108090645 | G | A | 1 | a0001c0002t0002g0043 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1443+1022G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108090645 | |||||||
| chr11:108090653 | A | G | 2 | a0001c0002t0004g0198 a0001c0002t0011g0197 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1443+1030A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108090653 | |||||||
| chr11:108090900 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1443+1277A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108090900 | |||||||
| chr11:108091022 | C | T | 8 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1443+1399C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091022 | |||||||
| chr11:108091040 | C | T | 287 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(284): Show |
297 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.1443+1417C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091040 | |||||||
| chr11:108091101 | G | C | 19 | a0001c0001t0001g0194 a0001c0001t0002g0010 a0001c0001t0002g0234 others(16): Show |
20 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1443+1478G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091101 | |||||||
| chr11:108091103 | T | C | 1 | a0001c0002t0032g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1443+1480T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091103 | |||||||
| chr11:108091115 | A | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1443+1492A>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091115 | |||||||
| chr11:108091128 | T | C | 1 | a0001c0001t0020g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1443+1505T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091128 | |||||||
| chr11:108091293 | C | T | 53 | a0001c0001t0001g0194 a0001c0001t0002g0010 a0001c0001t0002g0234 others(50): Show |
56 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1443+1670C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091293 | |||||||
| chr11:108091367 | T | TA | 92 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
96 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1443+1754dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091367 | ||||||
| chr11:108091380 | T | A | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1443+1757T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091380 | |||||||
| chr11:108091477 | G | C | 31 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(28): Show |
31 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.1443+1854G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091477 | |||||||
| chr11:108091695 | T | TCA | 43 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0093 others(40): Show |
44 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1443+2108_1443+210 others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | T | TCACA | 52 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(49): Show |
54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1443+2106_1443+210 others(8): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | T | TCACACA | 32 | a0001c0001t0001g0161 a0001c0001t0001g0194 a0001c0001t0001g0226 others(29): Show |
34 | HG00544.hp1 HG00733.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1443+2104_1443+210 others(10): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | T | TCACACAC others(1): Show |
22 | a0001c0001t0001g0229 a0001c0001t0001g0287 a0001c0002t0002g0035 others(19): Show |
23 | HG00558.hp2 HG00639.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1443+2102_1443+210 others(12): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | T | TCACACAC others(3): Show |
23 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0002t0002g0043 others(20): Show |
23 | HG00741.hp2 HG02602.hp1 HG02683.hp2 others(20): Show |
intron_variant | MODIFIER | c.1443+2100_1443+210 others(14): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | T | TCACACAC others(5): Show |
17 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1443+2098_1443+210 others(16): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | T | TCACACAC others(7): Show |
8 | a0001c0002t0002g0047 a0001c0002t0004g0071 a0001c0002t0004g0077 others(5): Show |
9 | HG00280.hp1 HG01981.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1443+2096_1443+210 others(18): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | T | TCACACAC others(9): Show |
2 | a0001c0002t0003g0187 a0001c0002t0004g0075 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1443+2094_1443+210 others(20): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | T | TCACACAC others(11): Show |
2 | a0001c0002t0004g0072 a0001c0002t0004g0074 |
2 | HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1443+2092_1443+210 others(22): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | T | TCACACAC others(13): Show |
1 | a0001c0002t0004g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1443+2090_1443+210 others(24): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | TCA | T | 6 | a0001c0001t0001g0118 a0001c0001t0001g0273 a0001c0002t0004g0198 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1443+2108_1443+210 others(6): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | TCACA | T | 4 | a0001c0002t0009g0059 a0001c0002t0009g0060 a0001c0002t0009g0061 others(1): Show |
4 | HG02451.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1443+2106_1443+210 others(8): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091695 | TCACACAC others(5): Show |
T | 2 | a0001c0002t0031g0086 a0002c0008t0001g0141 |
2 | HG01123.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1443+2098_1443+210 others(16): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108091695 | ||||||
| chr11:108091732 | C | CACACACA others(4): Show |
1 | a0001c0002t0003g0186 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1443+2109_1443+211 others(15): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091732 | |||||||
| chr11:108091732 | C | T | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1443+2109C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091732 | |||||||
| chr11:108091805 | G | A | 53 | a0001c0001t0001g0194 a0001c0001t0002g0010 a0001c0001t0002g0234 others(50): Show |
56 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1443+2182G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091805 | |||||||
| chr11:108091874 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(86): Show |
93 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1443+2251C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108091874 | |||||||
| chr11:108092035 | G | C | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1444-2356G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108092035 | |||||||
| chr11:108092320 | G | A | 299 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
309 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.1444-2071G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108092320 | |||||||
| chr11:108092702 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1444-1689G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108092702 | |||||||
| chr11:108093004 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(92): Show |
99 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1444-1387A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108093004 | |||||||
| chr11:108093220 | A | G | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.1444-1171A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108093220 | |||||||
| chr11:108093275 | ATCT | A | 38 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(35): Show |
39 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.1444-1112_1444-111 others(7): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 108093275 | ||||||
| chr11:108093518 | A | G | 1 | a0001c0002t0008g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1444-873A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108093518 | |||||||
| chr11:108093761 | G | A | 1 | a0001c0002t0002g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1444-630G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108093761 | |||||||
| chr11:108093763 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1444-628A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108093763 | |||||||
| chr11:108093787 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1444-604C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108093787 | |||||||
| chr11:108093822 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1444-569G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108093822 | |||||||
| chr11:108094218 | C | T | 8 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(5): Show |
8 | HG01074.hp1 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1444-173C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108094218 | |||||||
| chr11:108094222 | T | C | 1 | a0001c0002t0027g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1444-169T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 13/18 | chr11 | 108094222 | |||||||
| chr11:108094535 | G | A | 88 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(85): Show |
89 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1567+21G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 14/18 | chr11 | 108094535 | |||||||
| chr11:108094663 | A | G | 1 | a0001c0002t0002g0033 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1567+149A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 14/18 | chr11 | 108094663 | |||||||
| chr11:108094724 | T | C | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1568-88T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 14/18 | chr11 | 108094724 | |||||||
| chr11:108095180 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1743+193G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 15/18 | chr11 | 108095180 | |||||||
| chr11:108095187 | A | G | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+200A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 15/18 | chr11 | 108095187 | |||||||
| chr11:108095313 | C | T | 10 | a0001c0002t0002g0051 a0001c0002t0002g0054 a0001c0002t0002g0056 others(7): Show |
10 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.1744-217C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 15/18 | chr11 | 108095313 | |||||||
| chr11:108095364 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1744-166T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 15/18 | chr11 | 108095364 | |||||||
| chr11:108095368 | C | T | 1 | a0001c0002t0002g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1744-162C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 15/18 | chr11 | 108095368 | |||||||
| chr11:108095747 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1905+56T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108095747 | |||||||
| chr11:108095850 | C | T | 1 | a0001c0002t0003g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1905+159C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108095850 | |||||||
| chr11:108095941 | C | G | 1 | a0001c0001t0014g0219 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1905+250C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108095941 | |||||||
| chr11:108095989 | G | A | 39 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(36): Show |
40 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.1905+298G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108095989 | |||||||
| chr11:108096092 | G | A | 2 | a0001c0006t0001g0115 a0001c0006t0001g0116 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1905+401G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108096092 | |||||||
| chr11:108096096 | GA | G | 6 | a0001c0001t0001g0295 a0001c0001t0010g0144 a0001c0002t0003g0171 others(3): Show |
6 | HG02965.hp2 HG02976.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1905+419delA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 108096096 | ||||||
| chr11:108096115 | G | GCA | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0021g0190 |
3 | HG01243.hp1 NA19005.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1905+440_1905+441d others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 108096115 | ||||||
| chr11:108096328 | T | TA | 24 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0020 others(21): Show |
26 | HG00423.hp1 HG00544.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1905+655dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 108096328 | ||||||
| chr11:108096328 | TA | T | 163 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(160): Show |
168 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.1905+655delA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 108096328 | ||||||
| chr11:108096375 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1905+684C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108096375 | |||||||
| chr11:108096489 | AT | A | 9 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0247 others(6): Show |
9 | HG01081.hp2 HG03471.hp2 HG03834.hp1 others(6): Show |
intron_variant | MODIFIER | c.1905+809delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 108096489 | ||||||
| chr11:108096490 | T | A | 2 | a0001c0001t0021g0190 a0001c0003t0005g0001 |
3 | HG01243.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1905+799T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108096490 | |||||||
| chr11:108096490 | T | G | 1 | a0001c0002t0007g0052 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1905+799T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108096490 | |||||||
| chr11:108096564 | C | CT | 6 | a0001c0001t0001g0114 a0001c0001t0001g0233 a0001c0001t0001g0239 others(3): Show |
6 | HG01109.hp1 HG03579.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.1905+900dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 108096564 | ||||||
| chr11:108096564 | CT | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0017 others(162): Show |
171 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1905+900delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 108096564 | ||||||
| chr11:108096564 | CTT | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0120 others(46): Show |
50 | HG00438.hp2 HG01069.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.1905+899_1905+900d others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 108096564 | ||||||
| chr11:108096564 | CTTT | C | 13 | a0001c0002t0003g0080 a0001c0002t0003g0166 a0001c0002t0003g0167 others(10): Show |
15 | HG01123.hp1 HG02109.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1905+898_1905+900d others(5): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 108096564 | ||||||
| chr11:108096601 | T | G | 1 | a0001c0002t0002g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1905+910T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108096601 | |||||||
| chr11:108096623 | A | G | 10 | a0001c0002t0002g0051 a0001c0002t0002g0054 a0001c0002t0002g0056 others(7): Show |
10 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.1905+932A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108096623 | |||||||
| chr11:108096781 | G | A | 39 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(36): Show |
40 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.1906-855G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108096781 | |||||||
| chr11:108096829 | A | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
298 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.1906-807A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108096829 | |||||||
| chr11:108096953 | A | G | 1 | a0001c0002t0003g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1906-683A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108096953 | |||||||
| chr11:108097009 | C | T | 31 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(28): Show |
31 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.1906-627C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108097009 | |||||||
| chr11:108097096 | C | G | 1 | a0001c0002t0032g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1906-540C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108097096 | |||||||
| chr11:108097147 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(94): Show |
101 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1906-489A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108097147 | |||||||
| chr11:108097170 | C | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA18947.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1906-466C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108097170 | |||||||
| chr11:108097197 | G | A | 1 | a0001c0002t0003g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1906-439G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108097197 | |||||||
| chr11:108097279 | G | C | 1 | a0001c0001t0028g0154 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1906-357G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108097279 | |||||||
| chr11:108097422 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1906-214T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108097422 | |||||||
| chr11:108097506 | A | T | 1 | a0001c0002t0003g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1906-130A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 16/18 | chr11 | 108097506 | |||||||
| chr11:108097793 | T | A | 11 | a0001c0002t0002g0051 a0001c0002t0002g0054 a0001c0002t0002g0056 others(8): Show |
11 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.2024+39T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 17/18 | chr11 | 108097793 | |||||||
| chr11:108097811 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2024+57T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 17/18 | chr11 | 108097811 | |||||||
| chr11:108098036 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
6 | HG00280.hp2 NA18946.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.2024+282G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 17/18 | chr11 | 108098036 | |||||||
| chr11:108098043 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2024+289G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 17/18 | chr11 | 108098043 | |||||||
| chr11:108098057 | C | T | 71 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0078 others(68): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2024+303C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 17/18 | chr11 | 108098057 | |||||||
| chr11:108098057 | CGTTTTTG others(5): Show |
C | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2024+320_2025-321d others(14): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 108098057 | ||||||
| chr11:108098068 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2024+314T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 17/18 | chr11 | 108098068 | |||||||
| chr11:108098237 | A | G | 4 | a0001c0001t0006g0008 a0001c0001t0006g0248 a0001c0001t0006g0266 others(1): Show |
5 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2025-169A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 17/18 | chr11 | 108098237 | |||||||
| chr11:108098241 | C | T | 1 | a0001c0002t0017g0178 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2025-165C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 17/18 | chr11 | 108098241 | |||||||
| chr11:108098254 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2025-152T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 17/18 | chr11 | 108098254 | |||||||
| chr11:108098573 | GT | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.2148+62delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 108098573 | ||||||
| chr11:108098573 | GTT | G | 15 | a0001c0001t0001g0101 a0001c0001t0001g0161 a0001c0002t0002g0048 others(12): Show |
15 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.2148+61_2148+62del others(2): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 108098573 | ||||||
| chr11:108098591 | T | A | 7 | a0001c0001t0001g0135 a0001c0002t0002g0043 a0001c0002t0005g0013 others(4): Show |
8 | HG00642.hp2 HG01981.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2148+62T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108098591 | |||||||
| chr11:108098718 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0142 |
2 | NA18973.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2148+189T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108098718 | |||||||
| chr11:108098721 | A | G | 1 | a0001c0007t0002g0207 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2148+192A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108098721 | |||||||
| chr11:108098811 | T | C | 40 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(37): Show |
41 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.2148+282T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108098811 | |||||||
| chr11:108099005 | C | CT | 197 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(194): Show |
201 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.2148+493dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 108099005 | ||||||
| chr11:108099005 | C | CTT | 98 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
102 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.2148+492_2148+493d others(4): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 108099005 | ||||||
| chr11:108099095 | C | T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG00738.hp1 HG01099.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2148+566C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099095 | |||||||
| chr11:108099129 | G | A | 88 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(85): Show |
89 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2148+600G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099129 | |||||||
| chr11:108099220 | G | C | 88 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(85): Show |
89 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2148+691G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099220 | |||||||
| chr11:108099252 | C | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
309 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.2148+723C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099252 | |||||||
| chr11:108099334 | C | G | 7 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 others(4): Show |
8 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2148+805C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099334 | |||||||
| chr11:108099418 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2148+889G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099418 | |||||||
| chr11:108099576 | G | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0120 others(14): Show |
18 | HG00438.hp2 HG02074.hp1 NA18946.hp2 others(15): Show |
intron_variant | MODIFIER | c.2148+1047G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099576 | |||||||
| chr11:108099620 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2148+1091C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099620 | |||||||
| chr11:108099726 | T | G | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+1197T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099726 | |||||||
| chr11:108099906 | A | AT | 5 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0031g0086 others(2): Show |
6 | HG02451.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2148+1392dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 108099906 | ||||||
| chr11:108099906 | A | T | 52 | a0001c0001t0001g0194 a0001c0001t0002g0010 a0001c0001t0002g0234 others(49): Show |
55 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2148+1377A>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099906 | |||||||
| chr11:108099906 | AT | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0111 a0001c0001t0001g0161 others(4): Show |
7 | HG01168.hp2 HG03225.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.2148+1392delT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 108099906 | ||||||
| chr11:108099907 | T | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02055.hp1 HG02148.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2148+1378T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099907 | |||||||
| chr11:108099908 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2148+1379T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108099908 | |||||||
| chr11:108100038 | T | C | 10 | a0001c0002t0002g0051 a0001c0002t0002g0054 a0001c0002t0002g0056 others(7): Show |
10 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.2148+1509T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100038 | |||||||
| chr11:108100105 | G | GT | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(88): Show |
95 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.2148+1582dupT | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 108100105 | ||||||
| chr11:108100122 | A | G | 2 | a0001c0002t0002g0040 a0001c0002t0002g0047 |
2 | HG00280.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.2148+1593A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100122 | |||||||
| chr11:108100191 | C | T | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+1662C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100191 | |||||||
| chr11:108100259 | T | G | 40 | a0001c0002t0003g0080 a0001c0002t0003g0087 a0001c0002t0003g0088 others(37): Show |
41 | HG00741.hp2 HG01123.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.2148+1730T>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100259 | |||||||
| chr11:108100260 | A | G | 10 | a0001c0002t0002g0051 a0001c0002t0002g0054 a0001c0002t0002g0056 others(7): Show |
10 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.2148+1731A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100260 | |||||||
| chr11:108100306 | G | T | 1 | a0001c0001t0001g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2148+1777G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100306 | |||||||
| chr11:108100326 | T | C | 1 | a0001c0002t0002g0033 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2148+1797T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100326 | |||||||
| chr11:108100351 | T | A | 18 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0035 others(15): Show |
20 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.2148+1822T>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100351 | |||||||
| chr11:108100416 | G | A | 11 | a0001c0001t0002g0010 a0001c0001t0002g0234 a0001c0001t0002g0254 others(8): Show |
12 | HG01070.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2148+1887G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100416 | |||||||
| chr11:108100623 | A | G | 18 | a0001c0002t0002g0003 a0001c0002t0002g0033 a0001c0002t0002g0035 others(15): Show |
20 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.2148+2094A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100623 | |||||||
| chr11:108100686 | G | A | 1 | a0001c0002t0003g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2148+2157G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100686 | |||||||
| chr11:108100802 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02055.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2148+2273G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100802 | |||||||
| chr11:108100893 | G | A | 3 | a0001c0002t0013g0202 a0001c0002t0013g0203 a0001c0002t0013g0204 |
3 | HG02258.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2148+2364G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100893 | |||||||
| chr11:108100902 | G | A | 1 | a0001c0001t0006g0266 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2148+2373G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100902 | |||||||
| chr11:108100977 | G | C | 1 | a0001c0002t0002g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2148+2448G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108100977 | |||||||
| chr11:108101133 | A | G | 5 | a0001c0002t0009g0058 a0001c0002t0009g0059 a0001c0002t0009g0060 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2148+2604A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108101133 | |||||||
| chr11:108101173 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2148+2644T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108101173 | |||||||
| chr11:108101203 | T | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(286): Show |
299 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(296): Show |
intron_variant | MODIFIER | c.2148+2674T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108101203 | |||||||
| chr11:108101235 | G | A | 1 | a0001c0002t0010g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2148+2706G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108101235 | |||||||
| chr11:108101433 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2149-2757A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108101433 | |||||||
| chr11:108101523 | G | T | 1 | a0001c0001t0001g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2149-2667G>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108101523 | |||||||
| chr11:108101590 | C | T | 1 | a0001c0002t0003g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2149-2600C>T | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108101590 | |||||||
| chr11:108101694 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2149-2496G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108101694 | |||||||
| chr11:108101887 | TCTTC | T | 5 | a0001c0001t0001g0126 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG00438.hp2 NA18946.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2149-2298_2149-229 others(8): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 108101887 | ||||||
| chr11:108102082 | T | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(286): Show |
299 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(296): Show |
intron_variant | MODIFIER | c.2149-2108T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108102082 | |||||||
| chr11:108102159 | T | C | 8 | a0001c0002t0003g0080 a0001c0002t0003g0166 a0001c0002t0003g0167 others(5): Show |
8 | HG01123.hp1 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2149-2031T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108102159 | |||||||
| chr11:108102392 | T | C | 3 | a0001c0002t0013g0202 a0001c0002t0013g0203 a0001c0002t0013g0204 |
3 | HG02258.hp1 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2149-1798T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108102392 | |||||||
| chr11:108102451 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0294 |
2 | HG01192.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2149-1739T>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108102451 | |||||||
| chr11:108102528 | G | A | 2 | a0001c0002t0004g0026 a0001c0002t0025g0027 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2149-1662G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108102528 | |||||||
| chr11:108102570 | A | G | 1 | a0001c0006t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2149-1620A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108102570 | |||||||
| chr11:108102635 | A | G | 1 | a0001c0002t0003g0088 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2149-1555A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108102635 | |||||||
| chr11:108102828 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2149-1362G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108102828 | |||||||
| chr11:108103035 | A | G | 2 | a0001c0001t0001g0269 a0001c0002t0002g0054 |
2 | HG00558.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2149-1155A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103035 | |||||||
| chr11:108103104 | C | G | 7 | a0001c0002t0004g0071 a0001c0002t0004g0072 a0001c0002t0004g0073 others(4): Show |
7 | HG01074.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2149-1086C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103104 | |||||||
| chr11:108103191 | A | G | 1 | a0001c0002t0002g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2149-999A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103191 | |||||||
| chr11:108103213 | C | A | 1 | a0001c0001t0001g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2149-977C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103213 | |||||||
| chr11:108103285 | G | A | 27 | a0001c0001t0001g0019 a0001c0001t0001g0078 a0001c0001t0001g0089 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.2149-905G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103285 | |||||||
| chr11:108103312 | G | A | 1 | a0001c0002t0003g0181 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2149-878G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103312 | |||||||
| chr11:108103327 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
232 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.2149-863A>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103327 | |||||||
| chr11:108103366 | C | G | 1 | a0001c0002t0030g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2149-824C>G | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103366 | |||||||
| chr11:108103415 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
232 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.2149-775G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103415 | |||||||
| chr11:108103415 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2149-775G>C | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103415 | |||||||
| chr11:108103446 | G | GTTTTAAT others(5): Show |
3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149-743_2149-742i others(14): Show |
CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 108103446 | ||||||
| chr11:108103448 | C | A | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149-742C>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103448 | |||||||
| chr11:108103451 | T | TA | 3 | a0001c0002t0030g0302 a0001c0004t0012g0005 a0001c0004t0012g0082 |
4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149-738dupA | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 108103451 | ||||||
| chr11:108103699 | G | A | 4 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG01081.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149-491G>A | CUL5 | ENSG00000166266.14 | transcript | ENST00000393094.7 | protein_coding | 18/18 | chr11 | 108103699 |