Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 339761 |
| ensemblid | ENSG00000186684.14 |
| hgncid | 33480 |
| symbol | CYP27C1 |
| name | cytochrome P450 family 27 subfamily C member 1 |
| refseq_nuc | NM_001367502.1 |
| refseq_prot | NP_001354431.1 |
| ensembl_nuc | ENST00000664447.2 |
| ensembl_prot | ENSP00000499243.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 127183832 |
| end | 127220299 |
| strand | - |
| ver | v1.2 |
| region | chr2:127183832-127220299 |
| region5000 | chr2:127178832-127225299 |
| regionname0 | CYP27C1_chr2_127183832_127220299 |
| regionname5000 | CYP27C1_chr2_127178832_127225299 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 537 | 322 | 73 | 68 | 129 | 10 | 41 | 91 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | MALLA others(532): Show |
chr2 | 127178832 | 127225299 |
| a0002 | 0/0 | 537 | 15 | 14 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | MALLA others(532): Show |
chr2 | 127178832 | 127225299 |
| a0003 | 0/0 | 537 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | MALLA others(532): Show |
chr2 | 127178832 | 127225299 |
| a0004 | 0/0 | 537 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | MALLA others(532): Show |
chr2 | 127178832 | 127225299 |
| a0005 | 0/0 | 537 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | MALLA others(532): Show |
chr2 | 127178832 | 127225299 |
| a0006 | 0/0 | 537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | MALLA others(532): Show |
chr2 | 127178832 | 127225299 |
| a0007 | 0/0 | 537 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | MALLA others(532): Show |
chr2 | 127178832 | 127225299 |
| a0008 | 0/0 | 537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | MALLA others(532): Show |
chr2 | 127178832 | 127225299 |
| a0009 | 0/1 | 537 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | MALLA others(532): Show |
chr2 | 127178832 | 127225299 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1611 | 240 | 41 | 52 | 112 | 7 | 27 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0001c0002 | 0/0 | 1611 | 75 | 31 | 10 | 17 | 3 | 14 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0001c0005 | 0/0 | 1611 | 5 | 0 | 5 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0001c0012 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0001c0014 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0002c0003 | 0/0 | 1611 | 8 | 7 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0002c0004 | 0/0 | 1611 | 7 | 7 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0003c0006 | 0/0 | 1611 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0003c0008 | 0/0 | 1611 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0003c0010 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0004c0007 | 0/0 | 1611 | 3 | 2 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0005c0009 | 0/0 | 1611 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0006c0011 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0007c0016 | 0/0 | 1611 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0008c0015 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 | ||
| a0009c0013 | 0/1 | 1611 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | ATGGC others(1606): Show |
chr2 | 127178832 | 127225299 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5083 | 108 | 15 | 27 | 52 | 3 | 11 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0002 | 0/0 | 5087 | 75 | 3 | 19 | 39 | 4 | 10 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0003 | 0/0 | 5088 | 18 | 10 | 4 | 4 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5083): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0005 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5088): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0006 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0008 | 0/0 | 5078 | 4 | 4 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0010 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0012 | 0/0 | 5092 | 4 | 2 | 0 | 1 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5087): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0013 | 1/0 | 5082 | 4 | 0 | 1 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5077): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0015 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0021 | 0/0 | 5083 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0023 | 0/0 | 5083 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0024 | 0/0 | 5087 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0025 | 0/0 | 5087 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0030 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5088): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0033 | 0/0 | 5083 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0034 | 0/0 | 5083 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0035 | 0/0 | 5083 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0036 | 0/0 | 5083 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0038 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0040 | 0/0 | 5078 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0043 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0044 | 0/0 | 5092 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5087): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0045 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0046 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0047 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0048 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0049 | 0/0 | 5077 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5072): Show |
chr2 | 127178832 | 127225299 |
| a0001c0001t0050 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0001 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0004 | 0/0 | 5083 | 15 | 0 | 2 | 3 | 3 | 7 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0005 | 0/0 | 5093 | 11 | 0 | 1 | 8 | 0 | 2 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5088): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0006 | 0/0 | 5078 | 8 | 2 | 0 | 4 | 0 | 2 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0007 | 0/0 | 5078 | 11 | 6 | 3 | 0 | 0 | 2 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0009 | 0/0 | 5078 | 6 | 6 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0011 | 0/0 | 5083 | 5 | 4 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0014 | 0/0 | 5088 | 3 | 0 | 0 | 2 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5083): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0015 | 0/0 | 5083 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0016 | 0/0 | 5078 | 3 | 2 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0018 | 0/0 | 5088 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5083): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0022 | 0/0 | 5083 | 2 | 0 | 2 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0031 | 0/0 | 5088 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5083): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0032 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0037 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0039 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0001c0002t0042 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0001c0005t0002 | 0/0 | 5087 | 5 | 0 | 5 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0001c0012t0001 | 0/0 | 5083 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0001c0014t0008 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0002c0003t0003 | 0/0 | 5088 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5083): Show |
chr2 | 127178832 | 127225299 |
| a0002c0003t0006 | 0/0 | 5078 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0002c0003t0010 | 0/0 | 5078 | 4 | 4 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0002c0004t0019 | 0/0 | 5085 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5080): Show |
chr2 | 127178832 | 127225299 |
| a0002c0004t0020 | 0/0 | 5078 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0002c0004t0041 | 0/0 | 5080 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5075): Show |
chr2 | 127178832 | 127225299 |
| a0003c0006t0017 | 0/0 | 5057 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5052): Show |
chr2 | 127178832 | 127225299 |
| a0003c0006t0028 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5088): Show |
chr2 | 127178832 | 127225299 |
| a0003c0008t0008 | 0/0 | 5078 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5073): Show |
chr2 | 127178832 | 127225299 |
| a0003c0010t0029 | 0/0 | 5088 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5083): Show |
chr2 | 127178832 | 127225299 |
| a0004c0007t0002 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0004c0007t0026 | 0/0 | 5088 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5083): Show |
chr2 | 127178832 | 127225299 |
| a0004c0007t0027 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| a0005c0009t0003 | 0/0 | 5088 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5083): Show |
chr2 | 127178832 | 127225299 |
| a0006c0011t0002 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0007c0016t0002 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5082): Show |
chr2 | 127178832 | 127225299 |
| a0008c0015t0017 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5052): Show |
chr2 | 127178832 | 127225299 |
| a0009c0013t0001 | 0/1 | 5083 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | AGACA others(5078): Show |
chr2 | 127178832 | 127225299 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 1 | 2 | 5 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0003 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0007 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0012g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0012g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0013g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0013g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0013g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0013g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0015g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0021g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0021g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0023g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0023g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0024g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0025g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0025g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0030g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0033g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0034g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0035g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0036g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0038g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0040g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0043g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0044g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0045g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0046g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0047g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0048g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0049g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0001t0050g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0006g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0006g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0007g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0007g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0007g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0007g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0007g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0011g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0014g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0014g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0014g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0015g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0015g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0016g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0016g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0018g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0018g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0022g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0031g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0032g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0037g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0039g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0002t0042g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0005t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0005t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0005t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0005t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0005t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0012t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0001c0014t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0003t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0003t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0003t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0003t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0003t0010g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0003t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0003t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0004t0019g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0004t0019g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0004t0019g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0004t0020g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0004t0020g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0002c0004t0041g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0003c0006t0017g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0003c0006t0017g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0003c0006t0028g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0003c0008t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0003c0008t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0003c0010t0029g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0004c0007t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0004c0007t0026g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0004c0007t0027g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0005c0009t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0006c0011t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0007c0016t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0008c0015t0017g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| a0009c0013t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | FIN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00423 | hp1 | a0001 | c0001 | t0047 | g0056 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00609 | hp1 | a0001 | c0002 | t0004 | g0068 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00642 | hp2 | a0001 | c0005 | t0002 | g0236 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01069 | hp1 | a0001 | c0005 | t0002 | g0127 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01069 | hp2 | a0001 | c0001 | t0040 | g0213 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01071 | hp1 | a0001 | c0005 | t0002 | g0119 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01168 | hp1 | a0006 | c0011 | t0002 | g0033 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01168 | hp2 | a0001 | c0002 | t0007 | g0094 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01169 | hp1 | a0001 | c0002 | t0007 | g0095 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01175 | hp2 | a0001 | c0002 | t0016 | g0294 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01192 | hp2 | a0001 | c0002 | t0004 | g0098 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01243 | hp1 | a0002 | c0003 | t0003 | g0040 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01243 | hp2 | a0001 | c0002 | t0011 | g0012 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01256 | hp1 | a0001 | c0002 | t0022 | g0015 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01258 | hp1 | a0001 | c0002 | t0022 | g0015 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01346 | hp2 | a0001 | c0005 | t0002 | g0047 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01433 | hp1 | a0001 | c0012 | t0001 | g0100 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01433 | hp2 | a0001 | c0005 | t0002 | g0237 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01515 | hp1 | a0001 | c0002 | t0004 | g0013 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0013 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01884 | hp1 | a0001 | c0002 | t0009 | g0072 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01891 | hp1 | a0001 | c0002 | t0009 | g0090 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01891 | hp2 | a0001 | c0002 | t0007 | g0297 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01943 | hp1 | a0001 | c0001 | t0013 | g0061 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0049 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0280 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02015 | hp1 | a0001 | c0001 | t0023 | g0197 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02015 | hp2 | a0001 | c0002 | t0006 | g0102 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02027 | hp2 | a0001 | c0002 | t0005 | g0055 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02055 | hp2 | a0001 | c0002 | t0011 | g0012 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02056 | hp1 | a0001 | c0001 | t0036 | g0190 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02056 | hp2 | a0001 | c0001 | t0024 | g0018 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02071 | hp2 | a0001 | c0002 | t0004 | g0097 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02074 | hp2 | a0001 | c0002 | t0005 | g0085 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02132 | hp2 | a0001 | c0001 | t0043 | g0163 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0178 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02145 | hp2 | a0002 | c0003 | t0010 | g0010 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | CDX | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CDX | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | CDX | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02257 | hp1 | a0001 | c0002 | t0007 | g0025 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02257 | hp2 | a0001 | c0002 | t0016 | g0296 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02258 | hp2 | a0001 | c0002 | t0015 | g0291 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0282 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02280 | hp1 | a0001 | c0002 | t0006 | g0101 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02280 | hp2 | a0002 | c0003 | t0010 | g0010 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02293 | hp1 | a0001 | c0002 | t0007 | g0096 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02615 | hp1 | a0002 | c0004 | t0019 | g0034 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02615 | hp2 | a0001 | c0002 | t0018 | g0182 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0078 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02622 | hp2 | a0001 | c0002 | t0039 | g0067 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0074 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02630 | hp2 | a0002 | c0004 | t0041 | g0043 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02647 | hp1 | a0001 | c0002 | t0006 | g0058 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02647 | hp2 | a0003 | c0006 | t0028 | g0029 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02683 | hp1 | a0001 | c0002 | t0014 | g0082 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02683 | hp2 | a0001 | c0002 | t0004 | g0077 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0174 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02723 | hp2 | a0001 | c0002 | t0007 | g0025 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02738 | hp1 | a0001 | c0002 | t0004 | g0109 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02738 | hp2 | a0007 | c0016 | t0002 | g0304 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02809 | hp1 | a0001 | c0002 | t0011 | g0064 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02809 | hp2 | a0001 | c0002 | t0009 | g0092 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02818 | hp1 | a0002 | c0004 | t0019 | g0036 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02818 | hp2 | a0001 | c0002 | t0018 | g0211 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02886 | hp1 | a0001 | c0002 | t0007 | g0298 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02896 | hp1 | a0003 | c0006 | t0017 | g0030 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02896 | hp2 | a0005 | c0009 | t0003 | g0020 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02897 | hp1 | a0001 | c0002 | t0009 | g0091 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02897 | hp2 | a0005 | c0009 | t0003 | g0020 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02922 | hp1 | a0001 | c0001 | t0038 | g0300 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0288 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02965 | hp1 | a0002 | c0003 | t0006 | g0044 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02970 | hp1 | a0001 | c0002 | t0011 | g0070 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02976 | hp2 | a0001 | c0002 | t0009 | g0051 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0063 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03041 | hp1 | a0001 | c0014 | t0008 | g0302 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03041 | hp2 | a0002 | c0004 | t0020 | g0011 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03098 | hp1 | a0003 | c0008 | t0008 | g0027 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03098 | hp2 | a0001 | c0001 | t0021 | g0284 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03130 | hp1 | a0004 | c0007 | t0027 | g0106 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03139 | hp1 | a0001 | c0001 | t0030 | g0206 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03139 | hp2 | a0002 | c0003 | t0006 | g0042 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03195 | hp2 | a0001 | c0002 | t0007 | g0104 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03209 | hp1 | a0002 | c0004 | t0019 | g0035 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03209 | hp2 | a0001 | c0002 | t0016 | g0295 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03225 | hp1 | a0002 | c0004 | t0020 | g0038 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03225 | hp2 | a0003 | c0008 | t0008 | g0028 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03239 | hp1 | a0001 | c0002 | t0007 | g0093 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03239 | hp2 | a0001 | c0002 | t0006 | g0099 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03453 | hp1 | a0001 | c0002 | t0018 | g0169 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03453 | hp2 | a0001 | c0002 | t0007 | g0290 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03486 | hp2 | a0002 | c0003 | t0010 | g0037 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03516 | hp1 | a0001 | c0002 | t0031 | g0065 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03516 | hp2 | a0001 | c0002 | t0015 | g0301 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03540 | hp1 | a0001 | c0002 | t0011 | g0069 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03540 | hp2 | a0003 | c0010 | t0029 | g0031 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03579 | hp1 | a0001 | c0002 | t0037 | g0052 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03579 | hp2 | a0002 | c0004 | t0020 | g0011 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03669 | hp1 | a0001 | c0001 | t0012 | g0135 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03669 | hp2 | a0001 | c0002 | t0005 | g0057 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03710 | hp1 | a0001 | c0002 | t0004 | g0066 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03710 | hp2 | a0001 | c0001 | t0049 | g0132 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03834 | hp2 | a0001 | c0002 | t0006 | g0087 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03927 | hp1 | a0001 | c0002 | t0004 | g0088 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03927 | hp2 | a0001 | c0001 | t0034 | g0271 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03942 | hp2 | a0001 | c0001 | t0045 | g0117 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG04115 | hp1 | a0001 | c0001 | t0044 | g0167 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG04199 | hp1 | a0001 | c0001 | t0048 | g0130 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG04199 | hp2 | a0001 | c0002 | t0004 | g0054 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG04228 | hp1 | a0001 | c0002 | t0005 | g0084 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | CHB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | CHB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | CHB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18906 | hp1 | a0001 | c0002 | t0042 | g0060 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18942 | hp1 | a0001 | c0001 | t0024 | g0018 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18942 | hp2 | a0001 | c0001 | t0025 | g0269 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18944 | hp2 | a0001 | c0002 | t0005 | g0137 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18947 | hp2 | a0001 | c0001 | t0012 | g0129 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18948 | hp1 | a0001 | c0002 | t0005 | g0086 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18949 | hp2 | a0001 | c0001 | t0035 | g0200 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18951 | hp1 | a0001 | c0002 | t0004 | g0075 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18957 | hp2 | a0001 | c0001 | t0013 | g0115 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18961 | hp1 | a0001 | c0002 | t0005 | g0083 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18962 | hp2 | a0001 | c0002 | t0014 | g0045 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18969 | hp1 | a0001 | c0001 | t0050 | g0147 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18974 | hp2 | a0001 | c0002 | t0005 | g0228 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18975 | hp1 | a0001 | c0001 | t0033 | g0239 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18978 | hp2 | a0001 | c0001 | t0023 | g0196 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18980 | hp1 | a0001 | c0002 | t0005 | g0080 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18982 | hp2 | a0001 | c0002 | t0006 | g0231 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18983 | hp1 | a0001 | c0001 | t0025 | g0208 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0188 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18991 | hp2 | a0001 | c0002 | t0006 | g0111 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19000 | hp2 | a0004 | c0007 | t0002 | g0126 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19007 | hp2 | a0001 | c0001 | t0013 | g0121 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19030 | hp2 | a0001 | c0002 | t0009 | g0299 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19057 | hp2 | a0001 | c0002 | t0014 | g0229 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19067 | hp2 | a0001 | c0002 | t0006 | g0103 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19085 | hp2 | a0001 | c0001 | t0046 | g0151 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19091 | hp1 | a0001 | c0002 | t0005 | g0156 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA19240 | hp2 | a0001 | c0001 | t0015 | g0071 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA20129 | hp2 | a0001 | c0001 | t0021 | g0283 | AFR | ASW | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA20752 | hp1 | a0001 | c0002 | t0004 | g0048 | EUR | TSI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA20905 | hp1 | a0001 | c0002 | t0004 | g0108 | SAS | GIH | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA20905 | hp2 | a0001 | c0002 | t0007 | g0252 | SAS | GIH | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01123 | hp1 | a0001 | c0002 | t0005 | g0081 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02109 | hp1 | a0003 | c0006 | t0017 | g0032 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0293 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02486 | hp1 | a0004 | c0007 | t0026 | g0105 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG02559 | hp2 | a0002 | c0003 | t0010 | g0039 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | USA | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| HG06807 | hp2 | a0008 | c0015 | t0017 | g0303 | AFR | USA | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA20300 | hp1 | a0002 | c0003 | t0006 | g0041 | AFR | USA | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | USA | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA21309 | hp1 | a0001 | c0002 | t0032 | g0286 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| homoSapiens | chm13v2 | a0009 | c0013 | t0001 | g0193 | REF | REF | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0062 | REF | REF | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127187314 | G | A | 1 | a0004 | 3 | HG02486.hp1 HG03130.hp1 NA19000.hp2 |
missense_variant | MODERATE | c.1571C>T | p.Thr524Met | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1600/5082 | 1571/1614 | 524/537 | chr2 | 127187314 | |||
| chr2:127193842 | C | G | 1 | a0005 | 2 | HG02896.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.1240G>C | p.Gly414Arg | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/9 | 1269/5082 | 1240/1614 | 414/537 | chr2 | 127193842 | |||
| chr2:127220110 | G | C | 1 | a0002 | 15 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
missense_variant | MODERATE | c.161C>G | p.Pro54Arg | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 190/5082 | 161/1614 | 54/537 | chr2 | 127220110 | |||
| chr2:127220111 | G | T | 1 | a0002 | 15 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
missense_variant | MODERATE | c.160C>A | p.Pro54Thr | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 189/5082 | 160/1614 | 54/537 | chr2 | 127220111 | |||
| chr2:127220143 | G | A | 1 | a0008 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.128C>T | p.Ala43Val | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 157/5082 | 128/1614 | 43/537 | chr2 | 127220143 | |||
| chr2:127220192 | G | A | 1 | a0007 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.79C>T | p.Pro27Ser | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 108/5082 | 79/1614 | 27/537 | chr2 | 127220192 | |||
| chr2:127220218 | C | T | 1 | a0006 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.53G>A | p.Arg18Gln | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 82/5082 | 53/1614 | 18/537 | chr2 | 127220218 | |||
| chr2:127220240 | C | G | 1 | a0003 | 6 | HG02109.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.31G>C | p.Gly11Arg | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 60/5082 | 31/1614 | 11/537 | chr2 | 127220240 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127193795 | C | T | 1 | a0001c0012 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.1287G>A | p.Pro429Pro | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/9 | 1316/5082 | 1287/1614 | 429/537 | chr2 | 127193795 | |||
| chr2:127193810 | G | T | 1 | a0003c0010 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1272C>A | p.Gly424Gly | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/9 | 1301/5082 | 1272/1614 | 424/537 | chr2 | 127193810 | |||
| chr2:127195478 | A | C | 6 | a0001c0002 a0001c0014 a0002c0004 others(3): Show |
88 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(85): Show |
synonymous_variant | LOW | c.1071T>G | p.Thr357Thr | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/9 | 1100/5082 | 1071/1614 | 357/537 | chr2 | 127195478 | |||
| chr2:127199415 | G | A | 1 | a0001c0005 | 5 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
synonymous_variant | LOW | c.1008C>T | p.Tyr336Tyr | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/9 | 1037/5082 | 1008/1614 | 336/537 | chr2 | 127199415 | |||
| chr2:127220034 | C | A | 1 | a0001c0014 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.237G>T | p.Ala79Ala | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 266/5082 | 237/1614 | 79/537 | chr2 | 127220034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127183982 | C | G | 1 | a0001c0001t0035 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3289G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 3289 | chr2 | 127183982 | ||||||
| chr2:127184066 | A | C | 1 | a0001c0001t0047 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3205T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 3205 | chr2 | 127184066 | ||||||
| chr2:127184222 | T | C | 27 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(24): Show |
176 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*3049A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 3049 | chr2 | 127184222 | ||||||
| chr2:127184422 | G | A | 1 | a0001c0001t0048 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2849C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2849 | chr2 | 127184422 | ||||||
| chr2:127184446 | T | G | 3 | a0001c0002t0018 a0002c0004t0019 a0002c0004t0041 |
7 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2825A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2825 | chr2 | 127184446 | ||||||
| chr2:127184474 | C | T | 3 | a0001c0002t0018 a0002c0004t0019 a0002c0004t0041 |
7 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2797G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2797 | chr2 | 127184474 | ||||||
| chr2:127184555 | A | G | 48 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(45): Show |
232 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*2716T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2716 | chr2 | 127184555 | ||||||
| chr2:127184595 | A | G | 1 | a0001c0001t0046 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2676T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2676 | chr2 | 127184595 | ||||||
| chr2:127184604 | G | T | 1 | a0001c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2667 | chr2 | 127184604 | ||||||
| chr2:127184655 | G | A | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0023 others(11): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2616C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2616 | chr2 | 127184655 | ||||||
| chr2:127184756 | C | T | 2 | a0004c0007t0026 a0004c0007t0027 |
2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2515G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2515 | chr2 | 127184756 | ||||||
| chr2:127184758 | C | T | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(16): Show |
159 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*2513G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2513 | chr2 | 127184758 | ||||||
| chr2:127184847 | G | A | 2 | a0001c0002t0031 a0001c0002t0037 |
2 | HG03516.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2424C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2424 | chr2 | 127184847 | ||||||
| chr2:127184934 | C | T | 1 | a0001c0001t0034 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2337G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2337 | chr2 | 127184934 | ||||||
| chr2:127184946 | A | C | 1 | a0001c0002t0007 | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2325T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2325 | chr2 | 127184946 | ||||||
| chr2:127185026 | C | T | 2 | a0004c0007t0026 a0004c0007t0027 |
2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2245G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2245 | chr2 | 127185026 | ||||||
| chr2:127185112 | G | A | 1 | a0001c0001t0038 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2159C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2159 | chr2 | 127185112 | ||||||
| chr2:127185197 | G | C | 1 | a0001c0002t0022 | 2 | HG01256.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2074C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2074 | chr2 | 127185197 | ||||||
| chr2:127185215 | C | T | 11 | a0001c0001t0006 a0001c0001t0033 a0001c0001t0045 others(8): Show |
42 | HG00609.hp1 HG01175.hp2 HG01192.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2056G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2056 | chr2 | 127185215 | ||||||
| chr2:127185440 | C | T | 1 | a0001c0002t0032 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1831G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1831 | chr2 | 127185440 | ||||||
| chr2:127185733 | GA | G | 2 | a0002c0004t0019 a0002c0004t0041 |
4 | HG02615.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1537delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1537 | chr2 | 127185733 | ||||||
| chr2:127185964 | C | T | 2 | a0001c0002t0009 a0001c0002t0039 |
7 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1307G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1307 | chr2 | 127185964 | ||||||
| chr2:127185978 | G | A | 5 | a0001c0001t0006 a0001c0002t0004 a0001c0002t0006 others(2): Show |
29 | HG00609.hp1 HG01192.hp2 HG01256.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1293C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1293 | chr2 | 127185978 | ||||||
| chr2:127186245 | TTTATTTA others(4): Show |
T | 2 | a0003c0006t0017 a0008c0015t0017 |
3 | HG02109.hp1 HG02896.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1015_*1025delTAAA others(7): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1015 | chr2 | 127186245 | ||||||
| chr2:127186302 | A | G | 2 | a0001c0002t0011 a0002c0004t0020 |
8 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*969T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 969 | chr2 | 127186302 | ||||||
| chr2:127186344 | G | A | 2 | a0001c0001t0010 a0002c0003t0010 |
5 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*927C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 927 | chr2 | 127186344 | ||||||
| chr2:127186369 | C | CATTTT | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0024 others(19): Show |
126 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*897_*901dupAAAAT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 901 | chr2 | 127186369 | ||||||
| chr2:127186369 | C | CATTTTAT others(3): Show |
6 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0030 others(3): Show |
19 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*892_*901dupAAAATA others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 901 | chr2 | 127186369 | ||||||
| chr2:127186369 | CATTTT | C | 16 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 others(13): Show |
51 | HG01069.hp2 HG01168.hp2 HG01169.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*897_*901delAAAAT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 897 | chr2 | 127186369 | ||||||
| chr2:127186369 | CATTTTAT others(8): Show |
C | 2 | a0003c0006t0017 a0008c0015t0017 |
3 | HG02109.hp1 HG02896.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*887_*901delAAAATA others(9): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 887 | chr2 | 127186369 | ||||||
| chr2:127186435 | TCA | T | 2 | a0002c0004t0019 a0002c0004t0041 |
4 | HG02615.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*834_*835delTG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 834 | chr2 | 127186435 | ||||||
| chr2:127186438 | C | A | 2 | a0002c0004t0019 a0002c0004t0041 |
4 | HG02615.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*833G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 833 | chr2 | 127186438 | ||||||
| chr2:127186451 | G | T | 1 | a0001c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 820 | chr2 | 127186451 | ||||||
| chr2:127186459 | G | A | 3 | a0001c0002t0018 a0002c0004t0019 a0002c0004t0041 |
7 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*812C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 812 | chr2 | 127186459 | ||||||
| chr2:127186460 | C | A | 1 | a0001c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*811G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 811 | chr2 | 127186460 | ||||||
| chr2:127186504 | C | T | 1 | a0001c0001t0024 | 2 | HG02056.hp2 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*767G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 767 | chr2 | 127186504 | ||||||
| chr2:127186551 | A | G | 7 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0044 others(4): Show |
20 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*720T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 720 | chr2 | 127186551 | ||||||
| chr2:127186681 | G | A | 1 | a0001c0001t0023 | 2 | HG02015.hp1 NA18978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*590C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 590 | chr2 | 127186681 | ||||||
| chr2:127186691 | G | A | 1 | a0001c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*580C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 580 | chr2 | 127186691 | ||||||
| chr2:127186703 | C | A | 1 | a0001c0001t0050 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 568 | chr2 | 127186703 | ||||||
| chr2:127186988 | G | C | 3 | a0001c0002t0007 a0001c0002t0011 a0002c0004t0020 |
19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*283C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 283 | chr2 | 127186988 | ||||||
| chr2:127187122 | A | G | 1 | a0001c0001t0043 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 149 | chr2 | 127187122 | ||||||
| chr2:127187137 | C | T | 2 | a0004c0007t0026 a0004c0007t0027 |
2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*134G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 134 | chr2 | 127187137 | ||||||
| chr2:127187205 | A | AC | 49 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(46): Show |
248 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*65_*66insG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 65 | chr2 | 127187205 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127187447 | C | G | 17 | a0001c0001t0005g0188 a0001c0001t0021g0283 a0001c0001t0021g0284 others(14): Show |
17 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1498-60G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127187447 | |||||||
| chr2:127187511 | C | T | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1498-124G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127187511 | |||||||
| chr2:127187550 | T | G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0257 a0001c0001t0001g0266 |
3 | HG00408.hp2 HG02083.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1498-163A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127187550 | |||||||
| chr2:127187729 | G | T | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1498-342C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127187729 | |||||||
| chr2:127187893 | T | C | 9 | a0001c0002t0007g0093 a0001c0002t0007g0094 a0001c0002t0007g0095 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1498-506A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127187893 | |||||||
| chr2:127188025 | C | T | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1498-638G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188025 | |||||||
| chr2:127188076 | C | A | 6 | a0001c0002t0009g0051 a0001c0002t0009g0072 a0001c0002t0009g0090 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-689G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188076 | |||||||
| chr2:127188095 | T | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0183 a0001c0001t0001g0222 others(5): Show |
10 | HG01169.hp2 HG01952.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1498-708A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188095 | |||||||
| chr2:127188137 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1498-750C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188137 | |||||||
| chr2:127188211 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(140): Show |
164 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1498-824C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188211 | |||||||
| chr2:127188229 | G | C | 1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1498-842C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188229 | |||||||
| chr2:127188310 | G | A | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1498-923C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188310 | |||||||
| chr2:127188434 | C | T | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1498-1047G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188434 | |||||||
| chr2:127188457 | T | G | 6 | a0001c0002t0011g0012 a0001c0002t0011g0064 a0001c0002t0011g0069 others(3): Show |
8 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1498-1070A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188457 | |||||||
| chr2:127188475 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0073 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1498-1088G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188475 | |||||||
| chr2:127188522 | GC | G | 34 | a0001c0001t0006g0079 a0001c0002t0004g0013 a0001c0002t0004g0048 others(31): Show |
36 | HG00609.hp1 HG01192.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.1498-1136delG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188522 | |||||||
| chr2:127188524 | C | G | 34 | a0001c0001t0006g0079 a0001c0002t0004g0013 a0001c0002t0004g0048 others(31): Show |
36 | HG00609.hp1 HG01192.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.1498-1137G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188524 | |||||||
| chr2:127188575 | G | A | 1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1498-1188C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188575 | |||||||
| chr2:127188668 | T | TTCCATCT others(321): Show |
1 | a0001c0002t0009g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1498-1282_1498-128 others(332): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188668 | |||||||
| chr2:127188668 | T | TTCCATCT others(331): Show |
3 | a0001c0002t0009g0051 a0001c0002t0009g0072 a0001c0002t0009g0091 |
3 | HG01884.hp1 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1498-1282_1498-128 others(342): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188668 | |||||||
| chr2:127188668 | T | TTCCATCT others(332): Show |
2 | a0001c0002t0009g0090 a0001c0002t0009g0299 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1498-1282_1498-128 others(343): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188668 | |||||||
| chr2:127188668 | T | TTCCATCT others(336): Show |
1 | a0001c0002t0039g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1498-1282_1498-128 others(347): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188668 | |||||||
| chr2:127188689 | T | G | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1498-1302A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188689 | |||||||
| chr2:127188750 | T | C | 16 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(13): Show |
19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1498-1363A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188750 | |||||||
| chr2:127188796 | T | C | 5 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0005t0002g0047 others(2): Show |
7 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-1409A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188796 | |||||||
| chr2:127188855 | T | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(208): Show |
238 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.1498-1468A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188855 | |||||||
| chr2:127188867 | G | T | 11 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(8): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1498-1480C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188867 | |||||||
| chr2:127188899 | T | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG00558.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1498-1512A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188899 | |||||||
| chr2:127188924 | T | C | 17 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(14): Show |
20 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1498-1537A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188924 | |||||||
| chr2:127188943 | G | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(208): Show |
238 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.1498-1556C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188943 | |||||||
| chr2:127188974 | C | T | 1 | a0001c0001t0049g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1498-1587G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188974 | |||||||
| chr2:127189018 | C | T | 1 | a0001c0002t0039g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1498-1631G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189018 | |||||||
| chr2:127189019 | A | G | 27 | a0001c0001t0006g0079 a0001c0002t0004g0013 a0001c0002t0004g0048 others(24): Show |
29 | HG00609.hp1 HG01192.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1498-1632T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189019 | |||||||
| chr2:127189028 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1498-1641G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189028 | |||||||
| chr2:127189082 | C | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0251 |
2 | NA19074.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1498-1695G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189082 | |||||||
| chr2:127189168 | GC | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(271): Show |
319 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.1498-1782delG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189168 | |||||||
| chr2:127189315 | C | G | 1 | a0003c0006t0028g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1498-1928G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189315 | |||||||
| chr2:127189436 | C | A | 1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1498-2049G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189436 | |||||||
| chr2:127189468 | G | A | 10 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(7): Show |
11 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498-2081C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189468 | |||||||
| chr2:127189535 | G | C | 16 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(13): Show |
19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1498-2148C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189535 | |||||||
| chr2:127189584 | G | A | 1 | a0001c0001t0012g0129 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1498-2197C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189584 | |||||||
| chr2:127189621 | T | TA | 6 | a0001c0002t0011g0012 a0001c0002t0011g0064 a0001c0002t0011g0069 others(3): Show |
8 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1498-2235dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189621 | |||||||
| chr2:127189621 | TA | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(175): Show |
201 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.1498-2235delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189621 | |||||||
| chr2:127189621 | TAA | T | 7 | a0001c0001t0001g0150 a0001c0001t0001g0202 a0001c0001t0001g0212 others(4): Show |
7 | HG01256.hp2 HG02004.hp1 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498-2236_1498-223 others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189621 | |||||||
| chr2:127189661 | G | T | 10 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(7): Show |
11 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498-2274C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189661 | |||||||
| chr2:127189831 | C | T | 17 | a0001c0001t0005g0188 a0001c0001t0021g0283 a0001c0001t0021g0284 others(14): Show |
17 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1498-2444G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189831 | |||||||
| chr2:127189876 | T | C | 31 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(28): Show |
35 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1498-2489A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189876 | |||||||
| chr2:127189944 | G | C | 1 | a0001c0001t0002g0124 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1498-2557C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189944 | |||||||
| chr2:127190133 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(120): Show |
144 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1498-2746C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190133 | |||||||
| chr2:127190147 | G | A | 1 | a0001c0001t0045g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1498-2760C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190147 | |||||||
| chr2:127190261 | T | TA | 6 | a0001c0002t0011g0012 a0001c0002t0011g0064 a0001c0002t0011g0069 others(3): Show |
8 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1497+2832dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190261 | |||||||
| chr2:127190261 | T | TAA | 10 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(7): Show |
11 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1497+2831_1497+283 others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190261 | |||||||
| chr2:127190262 | A | T | 11 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(8): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1497+2832T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190262 | |||||||
| chr2:127190271 | T | A | 16 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(13): Show |
19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+2823A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190271 | |||||||
| chr2:127190329 | CTCTTTTT others(4): Show |
C | 4 | a0001c0002t0009g0072 a0001c0002t0009g0090 a0001c0002t0009g0091 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497+2754_1497+276 others(15): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190329 | |||||||
| chr2:127190331 | CTTTTTTT others(5): Show |
C | 2 | a0001c0002t0009g0051 a0001c0002t0009g0299 |
2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1497+2751_1497+276 others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190331 | |||||||
| chr2:127190340 | T | TTTC | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(87): Show |
108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1497+2753_1497+275 others(7): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190340 | |||||||
| chr2:127190341 | T | TTC | 52 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0046 others(49): Show |
55 | HG01069.hp2 HG01123.hp1 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.1497+2752_1497+275 others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190341 | |||||||
| chr2:127190342 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(139): Show |
163 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1497+2752G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190342 | |||||||
| chr2:127190342 | CT | C | 23 | a0001c0001t0002g0152 a0001c0001t0043g0163 a0001c0002t0007g0025 others(20): Show |
26 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1497+2751delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190342 | |||||||
| chr2:127190342 | CTT | C | 14 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(11): Show |
15 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1497+2750_1497+275 others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190342 | |||||||
| chr2:127190382 | A | G | 16 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(13): Show |
19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+2712T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190382 | |||||||
| chr2:127190388 | G | A | 16 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(13): Show |
19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+2706C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190388 | |||||||
| chr2:127190406 | G | A | 3 | a0001c0002t0009g0072 a0001c0002t0009g0090 a0001c0002t0009g0091 |
3 | HG01884.hp1 HG01891.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1497+2688C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190406 | |||||||
| chr2:127190428 | T | C | 16 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(13): Show |
19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+2666A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190428 | |||||||
| chr2:127190430 | C | T | 10 | a0001c0002t0015g0291 a0001c0002t0015g0301 a0001c0002t0018g0169 others(7): Show |
10 | HG02258.hp2 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1497+2664G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190430 | |||||||
| chr2:127190562 | G | A | 9 | a0001c0002t0007g0093 a0001c0002t0007g0094 a0001c0002t0007g0095 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1497+2532C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190562 | |||||||
| chr2:127190565 | C | T | 10 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(7): Show |
11 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1497+2529G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190565 | |||||||
| chr2:127190717 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1497+2377G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190717 | |||||||
| chr2:127190760 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(282): Show |
330 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(327): Show |
intron_variant | MODIFIER | c.1497+2334C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190760 | |||||||
| chr2:127190804 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1497+2290C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190804 | |||||||
| chr2:127190871 | C | T | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1497+2223G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190871 | |||||||
| chr2:127190940 | TG | T | 3 | a0001c0002t0015g0291 a0001c0002t0015g0301 a0001c0014t0008g0302 |
3 | HG02258.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1497+2153delC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190940 | |||||||
| chr2:127190941 | G | GA | 33 | a0001c0001t0001g0214 a0001c0001t0003g0050 a0001c0001t0003g0175 others(30): Show |
34 | HG01123.hp1 HG01243.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1497+2152dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190941 | |||||||
| chr2:127190954 | A | G | 1 | a0001c0002t0009g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1497+2140T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190954 | |||||||
| chr2:127191023 | A | T | 16 | a0001c0002t0007g0025 a0001c0002t0007g0093 a0001c0002t0007g0094 others(13): Show |
19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+2071T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191023 | |||||||
| chr2:127191045 | G | A | 31 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(28): Show |
35 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1497+2049C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191045 | |||||||
| chr2:127191227 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1497+1867C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191227 | |||||||
| chr2:127191332 | T | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(298): Show |
349 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(346): Show |
intron_variant | MODIFIER | c.1497+1762A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191332 | |||||||
| chr2:127191360 | A | G | 1 | a0001c0005t0002g0236 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1497+1734T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191360 | |||||||
| chr2:127191475 | C | T | 3 | a0001c0002t0016g0294 a0001c0002t0016g0295 a0001c0002t0016g0296 |
3 | HG01175.hp2 HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1497+1619G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191475 | |||||||
| chr2:127191480 | C | T | 11 | a0001c0002t0007g0025 a0001c0002t0007g0104 a0001c0002t0007g0290 others(8): Show |
14 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1497+1614G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191480 | |||||||
| chr2:127191539 | T | C | 1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1497+1555A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191539 | |||||||
| chr2:127191565 | C | G | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1497+1529G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191565 | |||||||
| chr2:127191622 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(213): Show |
243 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.1497+1472T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191622 | |||||||
| chr2:127191698 | G | A | 4 | a0002c0004t0019g0034 a0002c0004t0019g0035 a0002c0004t0019g0036 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+1396C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191698 | |||||||
| chr2:127191729 | C | T | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1497+1365G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191729 | |||||||
| chr2:127191828 | C | T | 1 | a0001c0002t0006g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1497+1266G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191828 | |||||||
| chr2:127191852 | A | T | 1 | a0001c0002t0011g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1497+1242T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191852 | |||||||
| chr2:127191888 | G | T | 1 | a0001c0001t0001g0249 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1497+1206C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191888 | |||||||
| chr2:127191892 | C | G | 1 | a0001c0002t0031g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1497+1202G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191892 | |||||||
| chr2:127191929 | A | G | 3 | a0001c0001t0002g0160 a0001c0001t0002g0189 a0001c0001t0002g0255 |
3 | HG00609.hp2 HG02165.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1497+1165T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191929 | |||||||
| chr2:127192093 | C | T | 7 | a0001c0002t0015g0291 a0001c0002t0015g0301 a0001c0014t0008g0302 others(4): Show |
7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1497+1001G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192093 | |||||||
| chr2:127192201 | C | T | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1497+893G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192201 | |||||||
| chr2:127192262 | C | G | 1 | a0001c0002t0006g0231 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1497+832G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192262 | |||||||
| chr2:127192294 | T | C | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1497+800A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192294 | |||||||
| chr2:127192322 | T | G | 7 | a0001c0002t0007g0025 a0001c0002t0011g0012 a0001c0002t0011g0064 others(4): Show |
10 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+772A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192322 | |||||||
| chr2:127192374 | A | C | 8 | a0001c0002t0016g0294 a0001c0002t0016g0295 a0001c0002t0016g0296 others(5): Show |
8 | HG01175.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1497+720T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192374 | |||||||
| chr2:127192387 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1497+707A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192387 | |||||||
| chr2:127192439 | G | T | 9 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(6): Show |
10 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1497+655C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192439 | |||||||
| chr2:127192498 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(137): Show |
165 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.1497+596C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192498 | |||||||
| chr2:127192554 | G | T | 1 | a0001c0001t0001g0143 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1497+540C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192554 | |||||||
| chr2:127192616 | TC | T | 7 | a0001c0002t0007g0025 a0001c0002t0011g0012 a0001c0002t0011g0064 others(4): Show |
10 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+477delG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192616 | |||||||
| chr2:127192619 | CG | C | 69 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(66): Show |
72 | HG00609.hp1 HG01168.hp2 HG01169.hp1 others(69): Show |
intron_variant | MODIFIER | c.1497+474delC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192619 | |||||||
| chr2:127192619 | CGGG | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(115): Show |
139 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1497+472_1497+474d others(5): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192619 | |||||||
| chr2:127192623 | G | C | 56 | a0001c0002t0001g0289 a0001c0002t0004g0013 a0001c0002t0004g0049 others(53): Show |
58 | HG00609.hp1 HG01168.hp2 HG01169.hp1 others(55): Show |
intron_variant | MODIFIER | c.1497+471C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192623 | |||||||
| chr2:127192624 | G | A | 1 | a0001c0001t0012g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1497+470C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192624 | |||||||
| chr2:127192624 | G | T | 4 | a0001c0001t0002g0140 a0001c0001t0002g0159 a0004c0007t0026g0105 others(1): Show |
4 | HG02486.hp1 HG03130.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+470C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192624 | |||||||
| chr2:127192625 | G | A | 2 | a0001c0001t0002g0089 a0001c0001t0002g0110 |
2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1497+469C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192625 | |||||||
| chr2:127192625 | G | C | 7 | a0001c0002t0007g0025 a0001c0002t0011g0012 a0001c0002t0011g0064 others(4): Show |
10 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+469C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192625 | |||||||
| chr2:127192625 | G | T | 1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1497+469C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192625 | |||||||
| chr2:127192626 | G | C | 16 | a0001c0001t0005g0188 a0001c0002t0005g0055 a0001c0002t0005g0080 others(13): Show |
16 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1497+468C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192626 | |||||||
| chr2:127192630 | G | C | 7 | a0001c0002t0007g0025 a0001c0002t0011g0012 a0001c0002t0011g0064 others(4): Show |
10 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+464C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192630 | |||||||
| chr2:127192675 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1497+419G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192675 | |||||||
| chr2:127192751 | G | GC | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(135): Show |
163 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.1497+342dupG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192751 | |||||||
| chr2:127192756 | G | GCACCGCA others(326): Show |
1 | a0001c0001t0001g0250 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | |||||||
| chr2:127192756 | G | GCACCGCA others(326): Show |
7 | a0001c0002t0007g0025 a0001c0002t0011g0012 a0001c0002t0011g0064 others(4): Show |
10 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | |||||||
| chr2:127192756 | G | GCACCGCA others(326): Show |
9 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(6): Show |
10 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | |||||||
| chr2:127192756 | G | GCACCGCA others(326): Show |
2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG00558.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | |||||||
| chr2:127192756 | G | GCACCGCA others(326): Show |
118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(115): Show |
139 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | |||||||
| chr2:127192756 | G | GCACCGCA others(326): Show |
1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | |||||||
| chr2:127192808 | A | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(214): Show |
244 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.1497+286T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192808 | |||||||
| chr2:127192849 | C | T | 6 | a0001c0002t0011g0012 a0001c0002t0011g0064 a0001c0002t0011g0069 others(3): Show |
8 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1497+245G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192849 | |||||||
| chr2:127192867 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(117): Show |
141 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1497+227C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192867 | |||||||
| chr2:127193073 | C | T | 1 | a0001c0002t0007g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1497+21G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127193073 | |||||||
| chr2:127193328 | A | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(135): Show |
163 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.1294-31T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/8 | chr2 | 127193328 | |||||||
| chr2:127193421 | C | T | 29 | a0001c0002t0004g0013 a0001c0002t0004g0048 a0001c0002t0004g0049 others(26): Show |
31 | HG00609.hp1 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1294-124G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/8 | chr2 | 127193421 | |||||||
| chr2:127193449 | C | A | 1 | a0001c0002t0031g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1294-152G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/8 | chr2 | 127193449 | |||||||
| chr2:127193449 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1294-152G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/8 | chr2 | 127193449 | |||||||
| chr2:127193519 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(127): Show |
152 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.1294-222A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/8 | chr2 | 127193519 | |||||||
| chr2:127193882 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(138): Show |
166 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.1215-15C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127193882 | |||||||
| chr2:127193883 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(116): Show |
140 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1215-16G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127193883 | |||||||
| chr2:127193986 | G | C | 2 | a0001c0001t0021g0283 a0001c0001t0021g0284 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1215-119C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127193986 | |||||||
| chr2:127193994 | T | G | 1 | a0001c0002t0007g0096 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1215-127A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127193994 | |||||||
| chr2:127194170 | T | C | 8 | a0001c0002t0011g0012 a0001c0002t0011g0064 a0001c0002t0011g0069 others(5): Show |
10 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1215-303A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194170 | |||||||
| chr2:127194221 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(126): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1215-354G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194221 | |||||||
| chr2:127194258 | G | A | 9 | a0001c0002t0007g0025 a0001c0002t0011g0012 a0001c0002t0011g0064 others(6): Show |
12 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1215-391C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194258 | |||||||
| chr2:127194505 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(136): Show |
164 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1215-638G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194505 | |||||||
| chr2:127194555 | G | A | 2 | a0001c0001t0021g0283 a0001c0001t0021g0284 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1215-688C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194555 | |||||||
| chr2:127194617 | A | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(136): Show |
164 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1214+718T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194617 | |||||||
| chr2:127194630 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(136): Show |
164 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1214+705T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194630 | |||||||
| chr2:127194687 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(136): Show |
164 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1214+648A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194687 | |||||||
| chr2:127194710 | G | A | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1214+625C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194710 | |||||||
| chr2:127194842 | C | CT | 81 | a0001c0001t0001g0224 a0001c0002t0001g0289 a0001c0002t0004g0013 others(78): Show |
86 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(83): Show |
intron_variant | MODIFIER | c.1214+492dupA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194842 | |||||||
| chr2:127194868 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(136): Show |
164 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1214+467G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194868 | |||||||
| chr2:127194885 | G | C | 8 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(5): Show |
9 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1214+450C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194885 | |||||||
| chr2:127194956 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(127): Show |
152 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.1214+379T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194956 | |||||||
| chr2:127194997 | T | G | 7 | a0001c0002t0015g0291 a0001c0002t0015g0301 a0001c0014t0008g0302 others(4): Show |
7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214+338A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194997 | |||||||
| chr2:127195249 | G | A | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1214+86C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127195249 | |||||||
| chr2:127195582 | C | T | 9 | a0001c0002t0007g0025 a0001c0002t0011g0012 a0001c0002t0011g0064 others(6): Show |
12 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1048-81G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127195582 | |||||||
| chr2:127195841 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(128): Show |
153 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1048-340C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127195841 | |||||||
| chr2:127195879 | G | A | 7 | a0001c0002t0015g0291 a0001c0002t0015g0301 a0001c0014t0008g0302 others(4): Show |
7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1048-378C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127195879 | |||||||
| chr2:127195950 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1048-449C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127195950 | |||||||
| chr2:127196019 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1048-518T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196019 | |||||||
| chr2:127196065 | CT | C | 82 | a0001c0001t0002g0223 a0001c0002t0001g0289 a0001c0002t0004g0013 others(79): Show |
87 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(84): Show |
intron_variant | MODIFIER | c.1048-565delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196065 | |||||||
| chr2:127196065 | CTT | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(129): Show |
154 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.1048-566_1048-565d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196065 | |||||||
| chr2:127196080 | T | C | 26 | a0001c0002t0005g0055 a0001c0002t0005g0080 a0001c0002t0005g0081 others(23): Show |
29 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1048-579A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196080 | |||||||
| chr2:127196124 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1048-623C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196124 | |||||||
| chr2:127196212 | A | G | 26 | a0001c0002t0005g0055 a0001c0002t0005g0080 a0001c0002t0005g0081 others(23): Show |
29 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1048-711T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196212 | |||||||
| chr2:127196224 | G | A | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048-723C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196224 | |||||||
| chr2:127196262 | C | CTG | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(213): Show |
243 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.1048-763_1048-762d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196262 | |||||||
| chr2:127196298 | G | C | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1048-797C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196298 | |||||||
| chr2:127196318 | C | T | 26 | a0001c0002t0005g0055 a0001c0002t0005g0080 a0001c0002t0005g0081 others(23): Show |
29 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1048-817G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196318 | |||||||
| chr2:127196356 | C | T | 1 | a0003c0006t0028g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1048-855G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196356 | |||||||
| chr2:127196445 | G | A | 26 | a0001c0002t0005g0055 a0001c0002t0005g0080 a0001c0002t0005g0081 others(23): Show |
29 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1048-944C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196445 | |||||||
| chr2:127196464 | T | C | 1 | a0001c0001t0015g0071 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1048-963A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196464 | |||||||
| chr2:127196533 | CA | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(204): Show |
232 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(229): Show |
intron_variant | MODIFIER | c.1048-1033delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196533 | |||||||
| chr2:127196983 | A | AT | 6 | a0001c0002t0005g0055 a0001c0002t0005g0080 a0001c0002t0005g0083 others(3): Show |
6 | HG02027.hp2 HG02074.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1048-1483_1048-148 others(5): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196983 | |||||||
| chr2:127197046 | A | G | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048-1545T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197046 | |||||||
| chr2:127197063 | G | C | 1 | a0001c0001t0002g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1048-1562C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197063 | |||||||
| chr2:127197221 | A | G | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048-1720T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197221 | |||||||
| chr2:127197370 | C | T | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048-1869G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197370 | |||||||
| chr2:127197414 | C | T | 2 | a0004c0007t0026g0105 a0004c0007t0027g0106 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048-1913G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197414 | |||||||
| chr2:127197438 | G | A | 18 | a0001c0002t0005g0055 a0001c0002t0005g0080 a0001c0002t0005g0081 others(15): Show |
19 | HG01123.hp1 HG01891.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1048-1937C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197438 | |||||||
| chr2:127197441 | G | A | 23 | a0001c0002t0005g0055 a0001c0002t0005g0080 a0001c0002t0005g0081 others(20): Show |
25 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1047+1935C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197441 | |||||||
| chr2:127197442 | C | G | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1047+1934G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197442 | |||||||
| chr2:127197660 | C | T | 2 | a0001c0001t0003g0287 a0001c0001t0008g0288 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1047+1716G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197660 | |||||||
| chr2:127197706 | A | G | 1 | a0003c0010t0029g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1047+1670T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197706 | |||||||
| chr2:127197782 | C | A | 1 | a0001c0002t0006g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1047+1594G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197782 | |||||||
| chr2:127197784 | A | G | 5 | a0001c0002t0016g0294 a0001c0002t0016g0295 a0001c0002t0016g0296 others(2): Show |
6 | HG01175.hp2 HG02257.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1047+1592T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197784 | |||||||
| chr2:127197867 | C | T | 13 | a0001c0002t0005g0055 a0001c0002t0005g0080 a0001c0002t0005g0081 others(10): Show |
13 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1047+1509G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197867 | |||||||
| chr2:127197932 | G | A | 1 | a0003c0006t0017g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1047+1444C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197932 | |||||||
| chr2:127198073 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1047+1303A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198073 | |||||||
| chr2:127198110 | G | A | 4 | a0002c0004t0019g0034 a0002c0004t0019g0035 a0002c0004t0019g0036 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047+1266C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198110 | |||||||
| chr2:127198128 | T | C | 1 | a0001c0001t0021g0284 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1047+1248A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198128 | |||||||
| chr2:127198184 | G | GACACACA others(3): Show |
3 | a0001c0002t0009g0072 a0001c0002t0009g0090 a0001c0002t0042g0060 |
3 | HG01884.hp1 HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1047+1191_1047+119 others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198184 | |||||||
| chr2:127198184 | G | GACACACA others(5): Show |
1 | a0001c0002t0009g0091 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1047+1191_1047+119 others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198184 | |||||||
| chr2:127198186 | T | C | 7 | a0001c0001t0001g0076 a0001c0002t0009g0051 a0001c0002t0009g0072 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1047+1190A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | |||||||
| chr2:127198186 | T | TAC | 8 | a0001c0001t0001g0120 a0001c0001t0002g0131 a0001c0001t0002g0146 others(5): Show |
8 | HG00423.hp2 HG00558.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1047+1188_1047+118 others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | |||||||
| chr2:127198186 | T | TACAC | 4 | a0001c0001t0001g0212 a0001c0002t0018g0169 a0001c0002t0018g0182 others(1): Show |
4 | HG01256.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047+1186_1047+118 others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | |||||||
| chr2:127198186 | T | TACACAC | 43 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0046 others(40): Show |
48 | HG01069.hp2 HG01175.hp1 HG01175.hp2 others(45): Show |
intron_variant | MODIFIER | c.1047+1184_1047+118 others(10): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | |||||||
| chr2:127198186 | T | TACACACA others(1): Show |
110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(107): Show |
127 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1047+1182_1047+118 others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | |||||||
| chr2:127198186 | T | TACACACA others(3): Show |
24 | a0001c0001t0001g0022 a0001c0001t0001g0180 a0001c0001t0001g0181 others(21): Show |
26 | HG00609.hp1 HG00642.hp1 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.1047+1180_1047+118 others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | |||||||
| chr2:127198186 | T | TACACACA others(5): Show |
15 | a0001c0001t0001g0009 a0001c0001t0001g0219 a0001c0001t0001g0222 others(12): Show |
18 | HG01169.hp2 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1047+1178_1047+118 others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | |||||||
| chr2:127198186 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0183 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1047+1174_1047+118 others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | |||||||
| chr2:127198186 | TACAC | T | 6 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0089 others(3): Show |
9 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1047+1186_1047+118 others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | |||||||
| chr2:127198475 | T | C | 8 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(5): Show |
9 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1047+901A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198475 | |||||||
| chr2:127198542 | CT | C | 52 | a0001c0002t0004g0013 a0001c0002t0004g0048 a0001c0002t0004g0049 others(49): Show |
55 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.1047+833delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198542 | |||||||
| chr2:127198577 | A | ATGTTTTG others(41): Show |
1 | a0001c0001t0002g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1047+751_1047+798d others(50): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198577 | |||||||
| chr2:127198622 | A | C | 1 | a0001c0001t0001g0251 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1047+754T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198622 | |||||||
| chr2:127198628 | T | C | 3 | a0001c0002t0016g0294 a0001c0002t0016g0295 a0001c0002t0016g0296 |
3 | HG01175.hp2 HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1047+748A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198628 | |||||||
| chr2:127198638 | T | A | 1 | a0001c0001t0002g0154 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1047+738A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198638 | |||||||
| chr2:127198676 | A | C | 50 | a0001c0002t0004g0013 a0001c0002t0004g0048 a0001c0002t0004g0049 others(47): Show |
53 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(50): Show |
intron_variant | MODIFIER | c.1047+700T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198676 | |||||||
| chr2:127198693 | T | C | 3 | a0003c0006t0017g0030 a0003c0006t0017g0032 a0008c0015t0017g0303 |
3 | HG02109.hp1 HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1047+683A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198693 | |||||||
| chr2:127198833 | C | T | 3 | a0001c0001t0001g0185 a0001c0001t0001g0224 a0001c0001t0001g0256 |
3 | HG02040.hp1 HG04184.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1047+543G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198833 | |||||||
| chr2:127198835 | C | T | 3 | a0001c0002t0018g0169 a0001c0002t0018g0182 a0001c0002t0018g0211 |
3 | HG02615.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1047+541G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198835 | |||||||
| chr2:127198871 | C | A | 1 | a0001c0002t0037g0052 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1047+505G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198871 | |||||||
| chr2:127198967 | A | G | 47 | a0001c0002t0004g0013 a0001c0002t0004g0048 a0001c0002t0004g0049 others(44): Show |
50 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.1047+409T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198967 | |||||||
| chr2:127199002 | C | T | 1 | a0003c0006t0028g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1047+374G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199002 | |||||||
| chr2:127199015 | T | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0224 |
2 | HG04184.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1047+361A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199015 | |||||||
| chr2:127199055 | C | A | 3 | a0001c0002t0018g0169 a0001c0002t0018g0182 a0001c0002t0018g0211 |
3 | HG02615.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1047+321G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199055 | |||||||
| chr2:127199111 | C | A | 2 | a0002c0004t0020g0011 a0002c0004t0020g0038 |
3 | HG03041.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1047+265G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199111 | |||||||
| chr2:127199156 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1047+220C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199156 | |||||||
| chr2:127199236 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(118): Show |
142 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1047+140C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199236 | |||||||
| chr2:127199319 | G | T | 1 | a0001c0002t0004g0077 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1047+57C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199319 | |||||||
| chr2:127199607 | C | T | 5 | a0001c0002t0001g0289 a0001c0002t0007g0290 a0001c0002t0015g0291 others(2): Show |
5 | HG02258.hp2 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-68G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127199607 | |||||||
| chr2:127199708 | C | T | 5 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-169G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127199708 | |||||||
| chr2:127199747 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.884-208C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127199747 | |||||||
| chr2:127199852 | C | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(111): Show |
135 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.884-313G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127199852 | |||||||
| chr2:127200066 | G | A | 1 | a0008c0015t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.884-527C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200066 | |||||||
| chr2:127200128 | C | T | 9 | a0002c0003t0003g0040 a0002c0003t0006g0041 a0002c0003t0006g0042 others(6): Show |
9 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.884-589G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200128 | |||||||
| chr2:127200169 | G | A | 5 | a0001c0001t0001g0107 a0001c0001t0021g0283 a0001c0001t0021g0284 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-630C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200169 | |||||||
| chr2:127200242 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.884-703T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200242 | |||||||
| chr2:127200465 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(244): Show |
292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.883+657G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200465 | |||||||
| chr2:127200941 | C | T | 88 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(85): Show |
109 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.883+181G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200941 | |||||||
| chr2:127201414 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.674-83A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127201414 | |||||||
| chr2:127201488 | G | T | 2 | a0001c0001t0002g0089 a0001c0001t0002g0110 |
2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.674-157C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127201488 | |||||||
| chr2:127201883 | C | A | 8 | a0002c0003t0003g0040 a0002c0003t0006g0041 a0002c0003t0006g0042 others(5): Show |
8 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.674-552G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127201883 | |||||||
| chr2:127201921 | A | G | 2 | a0001c0002t0007g0297 a0001c0002t0007g0298 |
2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.674-590T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127201921 | |||||||
| chr2:127202039 | A | T | 1 | a0003c0006t0028g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.674-708T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202039 | |||||||
| chr2:127202067 | C | A | 1 | a0001c0001t0049g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.674-736G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202067 | |||||||
| chr2:127202084 | A | AT | 85 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(82): Show |
106 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.674-754dupA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202084 | |||||||
| chr2:127202084 | A | ATT | 15 | a0001c0001t0002g0123 a0001c0001t0002g0274 a0001c0005t0002g0047 others(12): Show |
15 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.674-755_674-754dup others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202084 | |||||||
| chr2:127202084 | AT | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0275 a0001c0002t0018g0169 others(2): Show |
6 | HG01516.hp2 HG01517.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.674-754delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202084 | |||||||
| chr2:127202156 | C | G | 1 | a0003c0006t0028g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.674-825G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202156 | |||||||
| chr2:127202255 | T | G | 98 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(95): Show |
119 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.674-924A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202255 | |||||||
| chr2:127202258 | G | A | 90 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(87): Show |
111 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.674-927C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202258 | |||||||
| chr2:127202617 | G | C | 5 | a0001c0002t0016g0294 a0001c0002t0016g0295 a0001c0002t0016g0296 others(2): Show |
5 | HG01175.hp2 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+755C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202617 | |||||||
| chr2:127202675 | C | G | 3 | a0001c0002t0015g0291 a0001c0002t0015g0301 a0001c0014t0008g0302 |
3 | HG02258.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.673+697G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202675 | |||||||
| chr2:127202743 | GT | G | 10 | a0001c0001t0001g0076 a0001c0001t0002g0116 a0001c0002t0009g0072 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.673+628delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202743 | |||||||
| chr2:127202744 | T | G | 2 | a0001c0001t0021g0283 a0001c0001t0021g0284 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.673+628A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202744 | |||||||
| chr2:127202747 | T | A | 1 | a0001c0002t0005g0057 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.673+625A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202747 | |||||||
| chr2:127202906 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.673+466A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202906 | |||||||
| chr2:127202915 | T | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0246 |
2 | HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.673+457A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202915 | |||||||
| chr2:127202948 | C | G | 4 | a0001c0001t0021g0283 a0001c0001t0021g0284 a0001c0002t0009g0092 others(1): Show |
4 | HG02615.hp1 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+424G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202948 | |||||||
| chr2:127202972 | G | T | 1 | a0001c0001t0049g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.673+400C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202972 | |||||||
| chr2:127202976 | T | G | 4 | a0001c0001t0008g0053 a0001c0001t0008g0074 a0001c0001t0008g0078 others(1): Show |
5 | HG01256.hp1 HG01258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+396A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202976 | |||||||
| chr2:127202993 | A | C | 3 | a0001c0001t0047g0056 a0001c0002t0006g0058 a0001c0002t0006g0101 |
3 | HG00423.hp1 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.673+379T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202993 | |||||||
| chr2:127202995 | T | C | 2 | a0001c0002t0006g0058 a0001c0002t0006g0101 |
2 | HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.673+377A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202995 | |||||||
| chr2:127203004 | T | G | 1 | a0001c0001t0002g0008 | 3 | HG00738.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.673+368A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203004 | |||||||
| chr2:127203090 | C | T | 11 | a0001c0001t0003g0287 a0001c0001t0008g0288 a0001c0002t0001g0289 others(8): Show |
13 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.673+282G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203090 | |||||||
| chr2:127203107 | G | T | 2 | a0001c0002t0007g0025 a0001c0002t0007g0297 |
3 | HG01891.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.673+265C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203107 | |||||||
| chr2:127203108 | C | T | 2 | a0001c0002t0007g0025 a0001c0002t0007g0297 |
3 | HG01891.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.673+264G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203108 | |||||||
| chr2:127203117 | A | G | 3 | a0001c0002t0015g0291 a0001c0002t0015g0301 a0001c0014t0008g0302 |
3 | HG02258.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.673+255T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203117 | |||||||
| chr2:127203169 | G | GA | 87 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(84): Show |
108 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.673+202dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203169 | |||||||
| chr2:127203169 | GA | G | 8 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0002g0227 others(5): Show |
8 | HG01168.hp2 HG01169.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.673+202delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203169 | |||||||
| chr2:127203694 | A | G | 2 | a0001c0002t0016g0295 a0001c0002t0016g0296 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.474-123T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203694 | |||||||
| chr2:127203729 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.474-158C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203729 | |||||||
| chr2:127203828 | T | C | 2 | a0001c0002t0001g0289 a0001c0002t0007g0290 |
2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.474-257A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203828 | |||||||
| chr2:127203864 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 |
4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-293A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203864 | |||||||
| chr2:127203903 | G | A | 1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474-332C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203903 | |||||||
| chr2:127203915 | T | A | 1 | a0001c0002t0004g0098 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.474-344A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203915 | |||||||
| chr2:127204015 | A | G | 1 | a0001c0002t0018g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.474-444T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204015 | |||||||
| chr2:127204031 | A | C | 1 | a0001c0002t0018g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.474-460T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204031 | |||||||
| chr2:127204253 | G | A | 3 | a0001c0002t0018g0169 a0003c0006t0017g0030 a0003c0006t0017g0032 |
3 | HG02109.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474-682C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204253 | |||||||
| chr2:127204282 | A | AAG | 9 | a0001c0001t0001g0185 a0001c0001t0003g0292 a0001c0002t0009g0092 others(6): Show |
9 | HG01175.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-713_474-712dup others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204282 | |||||||
| chr2:127204282 | A | G | 2 | a0001c0002t0006g0058 a0001c0002t0006g0101 |
2 | HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.474-711T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204282 | |||||||
| chr2:127204320 | A | AGGAG | 79 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(76): Show |
98 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.474-753_474-750dup others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204320 | |||||||
| chr2:127204320 | A | AGGAGGGA others(1): Show |
24 | a0001c0001t0044g0167 a0001c0002t0007g0025 a0001c0002t0007g0290 others(21): Show |
27 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.474-757_474-750dup others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204320 | |||||||
| chr2:127204320 | A | AGGAGGGA others(9): Show |
1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474-765_474-750dup others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204320 | |||||||
| chr2:127204320 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0002g0124 |
2 | HG02300.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.474-749T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204320 | |||||||
| chr2:127204346 | A | G | 1 | a0004c0007t0002g0126 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.474-775T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204346 | |||||||
| chr2:127204347 | G | A | 1 | a0004c0007t0002g0126 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.474-776C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204347 | |||||||
| chr2:127204350 | A | AG | 7 | a0001c0001t0001g0184 a0001c0001t0001g0225 a0001c0001t0002g0149 others(4): Show |
7 | HG01192.hp1 HG01934.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-780dupC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204350 | |||||||
| chr2:127204377 | GAGAA | G | 8 | a0001c0001t0003g0175 a0001c0001t0003g0179 a0001c0001t0003g0203 others(5): Show |
9 | HG02055.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-810_474-807del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204377 | |||||||
| chr2:127204388 | AAAAG | A | 15 | a0002c0003t0003g0040 a0002c0003t0006g0041 a0002c0003t0006g0042 others(12): Show |
17 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.474-821_474-818del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204388 | |||||||
| chr2:127204394 | AAGAG | A | 68 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(65): Show |
87 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.474-827_474-824del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204394 | |||||||
| chr2:127204421 | G | C | 2 | a0001c0001t0002g0161 a0001c0001t0002g0165 |
2 | HG00735.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.474-850C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204421 | |||||||
| chr2:127204423 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0002g0113 |
2 | NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.474-852C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204423 | |||||||
| chr2:127204430 | G | A | 1 | a0001c0001t0002g0113 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.474-859C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204430 | |||||||
| chr2:127204432 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.474-861T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204432 | |||||||
| chr2:127204440 | A | AAAAG | 7 | a0001c0001t0021g0284 a0001c0002t0004g0108 a0001c0002t0005g0084 others(4): Show |
7 | HG01346.hp2 HG02486.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-873_474-870dup others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | A | AAAAGAAA others(1): Show |
10 | a0001c0001t0047g0056 a0001c0002t0004g0054 a0001c0002t0004g0077 others(7): Show |
10 | HG00423.hp1 HG01168.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-877_474-870dup others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | A | AAAAGAAA others(5): Show |
10 | a0001c0002t0004g0048 a0001c0002t0004g0063 a0001c0002t0005g0057 others(7): Show |
10 | HG01891.hp1 HG02809.hp1 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-881_474-870dup others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | A | AAAAGAAA others(9): Show |
2 | a0001c0002t0005g0055 a0001c0002t0006g0103 |
2 | HG02027.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.474-885_474-870dup others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | A | AAAAGAAA others(17): Show |
1 | a0001c0002t0005g0081 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.474-893_474-870dup others(24): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | A | AAGAAAGA others(11): Show |
1 | a0001c0001t0021g0283 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.474-870_474-869ins others(18): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.474-869T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | AAAAG | A | 11 | a0001c0001t0001g0073 a0001c0001t0001g0107 a0001c0001t0001g0170 others(8): Show |
12 | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.474-873_474-870del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | AAAAGAAA others(1): Show |
A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0076 others(31): Show |
42 | HG00408.hp1 HG00438.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.474-877_474-870del others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | AAAAGAAA others(5): Show |
A | 14 | a0001c0001t0001g0183 a0001c0001t0001g0191 a0001c0001t0001g0201 others(11): Show |
14 | HG01515.hp2 HG01952.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.474-881_474-870del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | AAAAGAAA others(9): Show |
A | 1 | a0001c0002t0016g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.474-885_474-870del others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | AAAAGAAA others(13): Show |
A | 4 | a0001c0001t0001g0195 a0001c0001t0001g0250 a0001c0001t0001g0251 others(1): Show |
4 | NA18950.hp2 NA18984.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-889_474-870del others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204440 | AAAAGAAA others(17): Show |
A | 2 | a0001c0001t0038g0300 a0001c0002t0009g0299 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.474-893_474-870del others(24): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | |||||||
| chr2:127204443 | A | G | 1 | a0003c0008t0008g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-872T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204443 | |||||||
| chr2:127204448 | G | GAAAGA | 3 | a0001c0001t0001g0120 a0001c0001t0002g0118 a0001c0001t0002g0131 |
3 | HG00423.hp2 HG03490.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.474-882_474-878dup others(5): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204448 | |||||||
| chr2:127204451 | A | G | 1 | a0003c0008t0008g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.474-880T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204451 | |||||||
| chr2:127204452 | G | GA | 31 | a0001c0001t0001g0133 a0001c0001t0001g0150 a0001c0001t0002g0004 others(28): Show |
42 | HG00438.hp1 HG00558.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.474-882dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204452 | |||||||
| chr2:127204453 | AAAG | A | 25 | a0001c0001t0001g0138 a0001c0001t0002g0003 a0001c0001t0002g0007 others(22): Show |
33 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.474-885_474-883del others(3): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204453 | |||||||
| chr2:127204453 | AAAGAAAG | A | 7 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0002g0148 others(4): Show |
7 | HG00639.hp1 HG02132.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-889_474-883del others(7): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204453 | |||||||
| chr2:127204456 | GAAAGAAA others(4): Show |
G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG00558.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.474-896_474-886del others(11): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204456 | |||||||
| chr2:127204458 | AAGAAAGA others(90): Show |
A | 1 | a0001c0002t0018g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.474-984_474-888del others(97): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204458 | |||||||
| chr2:127204461 | AAAGAAAG others(25): Show |
A | 1 | a0001c0002t0009g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.474-922_474-891del others(32): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204461 | |||||||
| chr2:127204463 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0275 |
2 | HG01192.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.474-892T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204463 | |||||||
| chr2:127204464 | GAAA | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0254 a0001c0001t0002g0255 others(1): Show |
4 | HG00544.hp1 HG02717.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-896_474-894del others(3): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204464 | |||||||
| chr2:127204467 | A | AG | 37 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(34): Show |
43 | HG00642.hp2 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.474-897dupC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204467 | |||||||
| chr2:127204467 | A | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0184 a0001c0001t0001g0275 others(1): Show |
4 | HG01192.hp1 HG01934.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-896T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204467 | |||||||
| chr2:127204468 | GAAA | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(15): Show |
20 | HG00408.hp2 HG01169.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.474-900_474-898del others(3): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204468 | |||||||
| chr2:127204468 | GAAAGAAA others(44): Show |
G | 1 | a0001c0001t0001g0212 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.474-948_474-898del others(51): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204468 | |||||||
| chr2:127204469 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0002g0171 others(1): Show |
4 | HG00735.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-898T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204469 | |||||||
| chr2:127204469 | AAAGAAAG others(13): Show |
A | 1 | a0003c0008t0008g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-918_474-899del others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204469 | |||||||
| chr2:127204471 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(43): Show |
53 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.474-900T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204471 | |||||||
| chr2:127204473 | A | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0170 others(13): Show |
18 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.474-902T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204473 | |||||||
| chr2:127204475 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(58): Show |
73 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.474-904T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204475 | |||||||
| chr2:127204477 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(44): Show |
57 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.474-906T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204477 | |||||||
| chr2:127204479 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(57): Show |
71 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.474-908T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204479 | |||||||
| chr2:127204481 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(61): Show |
75 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.474-910T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204481 | |||||||
| chr2:127204483 | A | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(14): Show |
19 | HG00408.hp2 HG01169.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.474-912T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204483 | |||||||
| chr2:127204484 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0002g0171 a0006c0011t0002g0033 |
3 | HG00735.hp2 HG01168.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.474-913C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204484 | |||||||
| chr2:127204485 | A | AAAGAAAG others(12): Show |
1 | a0001c0002t0005g0085 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.474-915_474-914ins others(19): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | |||||||
| chr2:127204485 | A | AAAGAAAG others(25): Show |
1 | a0001c0001t0003g0287 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.474-915_474-914ins others(32): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | |||||||
| chr2:127204485 | A | AAAGAAAG others(13): Show |
1 | a0001c0002t0005g0086 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.474-915_474-914ins others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | |||||||
| chr2:127204485 | A | AAAGAAAG others(17): Show |
1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474-915_474-914ins others(24): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | |||||||
| chr2:127204485 | A | AAAGAAAG others(21): Show |
2 | a0001c0001t0008g0288 a0001c0002t0001g0289 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.474-915_474-914ins others(28): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | |||||||
| chr2:127204485 | A | AAAGAAAG others(9): Show |
1 | a0001c0002t0039g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.474-915_474-914ins others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | |||||||
| chr2:127204485 | A | AAAGAAAG others(7): Show |
1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474-915_474-914ins others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | |||||||
| chr2:127204485 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(67): Show |
81 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.474-914T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | |||||||
| chr2:127204485 | AAAGG | A | 2 | a0001c0002t0004g0013 a0001c0002t0004g0098 |
3 | HG01192.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.474-918_474-915del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | |||||||
| chr2:127204485 | AAAGGAAG others(1): Show |
A | 1 | a0001c0001t0002g0007 | 3 | HG01255.hp2 HG02486.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.474-922_474-915del others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | |||||||
| chr2:127204487 | AG | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(54): Show |
69 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.474-917delC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204487 | |||||||
| chr2:127204488 | G | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0186 a0001c0001t0001g0240 others(7): Show |
11 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.474-917C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204488 | |||||||
| chr2:127204488 | G | GAAAGAAA others(4): Show |
1 | a0001c0002t0007g0095 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.474-918_474-917ins others(11): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204488 | |||||||
| chr2:127204489 | G | A | 92 | a0001c0001t0001g0120 a0001c0001t0001g0143 a0001c0001t0001g0144 others(89): Show |
111 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.474-918C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204489 | |||||||
| chr2:127204492 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(61): Show |
74 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.474-921C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204492 | |||||||
| chr2:127204493 | G | A | 70 | a0001c0001t0001g0120 a0001c0001t0001g0143 a0001c0001t0001g0144 others(67): Show |
83 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.474-922C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204493 | |||||||
| chr2:127204496 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0026 others(46): Show |
57 | HG00408.hp1 HG00438.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.474-925C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204496 | |||||||
| chr2:127204497 | G | A | 27 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(24): Show |
31 | HG00280.hp2 HG00733.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.474-926C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204497 | |||||||
| chr2:127204500 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(69): Show |
80 | HG00558.hp2 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.474-929C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204500 | |||||||
| chr2:127204501 | G | A | 9 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0131 others(6): Show |
9 | HG01516.hp1 HG01891.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-930C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204501 | |||||||
| chr2:127204504 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(103): Show |
124 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.474-933C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204504 | |||||||
| chr2:127204505 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0131 a0003c0006t0017g0032 |
3 | HG01516.hp1 HG02109.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.474-934C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204505 | |||||||
| chr2:127204508 | A | G | 63 | a0001c0001t0001g0133 a0001c0001t0001g0138 a0001c0001t0001g0183 others(60): Show |
69 | HG00639.hp2 HG00733.hp1 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.474-937T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204508 | |||||||
| chr2:127204512 | A | G | 42 | a0001c0001t0001g0150 a0001c0001t0001g0195 a0001c0001t0001g0250 others(39): Show |
45 | HG00558.hp1 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.474-941T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204512 | |||||||
| chr2:127204513 | G | GA | 3 | a0001c0002t0007g0025 a0003c0006t0017g0030 a0003c0006t0028g0029 |
3 | HG02257.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.474-943dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204513 | |||||||
| chr2:127204515 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0232 a0001c0001t0001g0277 |
3 | HG01928.hp2 HG03471.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.474-944T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204515 | |||||||
| chr2:127204516 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(174): Show |
206 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.474-945C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204516 | |||||||
| chr2:127204516 | GGAAA | G | 10 | a0001c0001t0001g0144 a0001c0001t0002g0006 a0001c0001t0002g0017 others(7): Show |
10 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-949_474-946del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204516 | |||||||
| chr2:127204519 | A | G | 9 | a0001c0001t0001g0026 a0001c0001t0001g0184 a0001c0001t0001g0232 others(6): Show |
10 | HG01069.hp2 HG01192.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-948T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204519 | |||||||
| chr2:127204520 | A | G | 16 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0017 others(13): Show |
17 | HG00733.hp1 HG01981.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.474-949T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204520 | |||||||
| chr2:127204521 | GAA | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0275 a0001c0002t0014g0229 |
3 | NA19000.hp1 NA19057.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.474-952_474-951del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204521 | |||||||
| chr2:127204523 | A | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0046 others(23): Show |
28 | HG00408.hp2 HG00558.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.474-952T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204523 | |||||||
| chr2:127204524 | A | G | 10 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0016 others(7): Show |
11 | HG00639.hp2 HG01070.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.474-953T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204524 | |||||||
| chr2:127204525 | GAA | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0114 others(8): Show |
11 | HG00544.hp2 HG01928.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.474-956_474-955del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204525 | |||||||
| chr2:127204526 | A | G | 1 | a0001c0001t0050g0147 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.474-955T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204526 | |||||||
| chr2:127204527 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(62): Show |
74 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.474-956T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204527 | |||||||
| chr2:127204527 | AAGAAAGA others(5): Show |
A | 1 | a0001c0001t0002g0007 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.474-968_474-957del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204527 | |||||||
| chr2:127204528 | A | G | 6 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0131 others(3): Show |
6 | HG01081.hp1 HG01516.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-957T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204528 | |||||||
| chr2:127204529 | GAA | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0022 others(6): Show |
9 | HG00438.hp2 HG01169.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-960_474-959del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204529 | |||||||
| chr2:127204530 | AAAGAAAG others(4): Show |
A | 1 | a0001c0001t0002g0134 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.474-970_474-960del others(11): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204530 | |||||||
| chr2:127204531 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(99): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.474-960T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204531 | |||||||
| chr2:127204531 | AAGAAAGA others(1): Show |
A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0168 a0001c0001t0012g0129 others(1): Show |
4 | HG03017.hp2 HG03492.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-968_474-961del others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204531 | |||||||
| chr2:127204531 | AAGAAAGA others(5): Show |
A | 8 | a0001c0001t0002g0007 a0001c0001t0002g0136 a0001c0001t0002g0152 others(5): Show |
9 | HG00733.hp2 HG00735.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-972_474-961del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204531 | |||||||
| chr2:127204531 | AAGAAAGA others(9): Show |
A | 2 | a0001c0001t0002g0123 a0001c0001t0012g0293 |
2 | HG01261.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.474-976_474-961del others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204531 | |||||||
| chr2:127204532 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.474-961T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204532 | |||||||
| chr2:127204533 | GAA | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0177 a0001c0001t0001g0180 others(9): Show |
12 | HG01099.hp2 HG01109.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.474-964_474-963del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204533 | |||||||
| chr2:127204535 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(142): Show |
175 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.474-964T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204535 | |||||||
| chr2:127204535 | AAG | A | 3 | a0001c0002t0004g0048 a0001c0002t0004g0098 a0001c0002t0007g0290 |
3 | HG01192.hp2 HG03453.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.474-966_474-965del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204535 | |||||||
| chr2:127204537 | G | GAA | 4 | a0001c0001t0001g0265 a0001c0001t0003g0292 a0001c0001t0008g0288 others(1): Show |
4 | HG02922.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-967_474-966ins others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204537 | |||||||
| chr2:127204539 | G | A | 39 | a0001c0001t0001g0026 a0001c0001t0001g0195 a0001c0001t0001g0250 others(36): Show |
44 | HG00639.hp2 HG01070.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.474-968C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204539 | |||||||
| chr2:127204541 | G | A | 1 | a0008c0015t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.474-970C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204541 | |||||||
| chr2:127204543 | G | A | 23 | a0001c0001t0001g0026 a0001c0001t0001g0138 a0001c0001t0001g0251 others(20): Show |
24 | HG01081.hp1 HG01516.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.474-972C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204543 | |||||||
| chr2:127204545 | G | A | 1 | a0008c0015t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.474-974C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204545 | |||||||
| chr2:127204545 | GAGAGAGA others(15): Show |
G | 1 | a0001c0001t0048g0130 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.474-996_474-975del others(22): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204545 | |||||||
| chr2:127204547 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0133 others(20): Show |
27 | HG00558.hp1 HG00738.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.474-976C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | |||||||
| chr2:127204547 | G | GAAGAAAG others(6): Show |
1 | a0001c0001t0001g0001 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.474-977_474-976ins others(13): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | |||||||
| chr2:127204547 | GAGAGAGA others(5): Show |
G | 1 | a0001c0001t0002g0005 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.474-988_474-977del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | |||||||
| chr2:127204547 | GAGAGAGA others(9): Show |
G | 3 | a0001c0001t0001g0143 a0001c0001t0002g0006 a0001c0002t0005g0137 |
3 | HG00438.hp1 NA18944.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.474-992_474-977del others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | |||||||
| chr2:127204547 | GAGAGAGA others(13): Show |
G | 2 | a0001c0001t0002g0003 a0001c0001t0024g0018 |
2 | HG04204.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.474-996_474-977del others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | |||||||
| chr2:127204547 | GAGAGAGA others(17): Show |
G | 1 | a0001c0002t0007g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.474-1000_474-977de others(25): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | |||||||
| chr2:127204549 | GAGAGAGA others(3): Show |
G | 1 | a0001c0001t0002g0124 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.474-988_474-979del others(10): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204549 | |||||||
| chr2:127204551 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0026 others(43): Show |
55 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.474-980C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | |||||||
| chr2:127204551 | G | GAA | 5 | a0001c0001t0001g0046 a0001c0001t0001g0192 a0001c0001t0001g0256 others(2): Show |
5 | HG00280.hp2 HG01952.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-981_474-980ins others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | |||||||
| chr2:127204551 | G | GAAAGAAA others(3): Show |
3 | a0001c0001t0001g0001 a0001c0001t0003g0233 a0002c0004t0020g0011 |
3 | HG03579.hp2 HG04204.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.474-981_474-980ins others(10): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | |||||||
| chr2:127204551 | G | GAGAAAGA others(9): Show |
1 | a0002c0004t0020g0011 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474-981_474-980ins others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | |||||||
| chr2:127204551 | G | GAGAGAGA others(15): Show |
1 | a0002c0003t0003g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.474-981_474-980ins others(22): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | |||||||
| chr2:127204551 | G | GAGAGAGA others(17): Show |
1 | a0002c0003t0010g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.474-981_474-980ins others(24): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | |||||||
| chr2:127204551 | GAGAGAGA others(5): Show |
G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0017 |
3 | HG02723.hp1 NA18951.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474-992_474-981del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | |||||||
| chr2:127204553 | GAGAGAAA others(15): Show |
G | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.474-1004_474-983de others(23): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204553 | |||||||
| chr2:127204554 | AG | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0235 a0001c0002t0009g0051 |
3 | HG00558.hp2 HG02135.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.474-984delC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204554 | |||||||
| chr2:127204555 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(102): Show |
122 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.474-984C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAA | 14 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0194 others(11): Show |
17 | HG00408.hp1 HG01433.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.474-985_474-984ins others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAAAGAA | 3 | a0001c0001t0001g0076 a0001c0001t0002g0021 a0001c0002t0004g0068 |
3 | HG00609.hp1 HG02572.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.474-985_474-984ins others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAAAGA others(5): Show |
1 | a0001c0002t0006g0102 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.474-996_474-985dup others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAAAGA others(16): Show |
1 | a0002c0004t0019g0036 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.474-985_474-984ins others(23): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAAAGA others(15): Show |
1 | a0002c0003t0010g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.474-985_474-984ins others(22): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAAGAA others(4): Show |
1 | a0001c0001t0002g0021 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.474-985_474-984ins others(11): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAGAA | 3 | a0001c0001t0002g0113 a0001c0001t0047g0056 a0001c0002t0005g0055 |
3 | HG00423.hp1 HG02027.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.474-985_474-984ins others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAGAAA others(3): Show |
3 | a0001c0001t0001g0112 a0001c0002t0005g0083 a0001c0002t0005g0085 |
3 | HG02074.hp2 NA18961.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.474-985_474-984ins others(10): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAGAAA others(7): Show |
1 | a0001c0002t0005g0086 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.474-985_474-984ins others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAGAAA others(15): Show |
1 | a0001c0002t0004g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.474-985_474-984ins others(22): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAGAAA others(19): Show |
1 | a0002c0003t0010g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.474-985_474-984ins others(26): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAGAGA others(13): Show |
1 | a0001c0001t0002g0110 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.474-985_474-984ins others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAGAGA others(21): Show |
2 | a0002c0003t0006g0041 a0002c0003t0006g0044 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.474-985_474-984ins others(28): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | G | GAGAGAGA others(25): Show |
1 | a0002c0004t0020g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.474-985_474-984ins others(32): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | GAGAA | G | 7 | a0001c0001t0001g0107 a0001c0001t0008g0053 a0001c0001t0013g0061 others(4): Show |
7 | HG01123.hp1 HG01243.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.474-988_474-985del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | GAGAAAGA others(1): Show |
G | 4 | a0001c0001t0001g0073 a0001c0001t0002g0166 a0001c0001t0024g0018 others(1): Show |
4 | HG02056.hp2 HG03710.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-992_474-985del others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | GAGAAAGA others(5): Show |
G | 2 | a0001c0001t0002g0005 a0001c0002t0009g0091 |
2 | HG01516.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.474-996_474-985del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | GAGAAAGA others(9): Show |
G | 1 | a0001c0002t0006g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.474-1000_474-985de others(17): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204555 | GAGAAAGA others(13): Show |
G | 1 | a0001c0005t0002g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.474-1004_474-985de others(21): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | |||||||
| chr2:127204557 | GA | G | 4 | a0001c0001t0001g0262 a0001c0001t0034g0271 a0001c0001t0050g0147 others(1): Show |
4 | HG02683.hp2 HG03927.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-987delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204557 | |||||||
| chr2:127204557 | GAA | G | 9 | a0001c0001t0001g0183 a0001c0001t0001g0222 a0001c0001t0001g0250 others(6): Show |
9 | HG01884.hp2 HG01952.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-988_474-987del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204557 | |||||||
| chr2:127204557 | GAAAGAA | G | 3 | a0001c0001t0001g0264 a0001c0002t0005g0080 a0001c0002t0007g0104 |
3 | HG03195.hp2 NA18980.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.474-992_474-987del others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204557 | |||||||
| chr2:127204557 | GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0001g0201 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.474-996_474-987del others(10): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204557 | |||||||
| chr2:127204557 | GAAAGAAA others(7): Show |
G | 1 | a0003c0010t0029g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.474-1000_474-987de others(15): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204557 | |||||||
| chr2:127204559 | A | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0191 others(45): Show |
51 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.474-988T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204559 | |||||||
| chr2:127204563 | A | G | 22 | a0001c0001t0001g0107 a0001c0001t0001g0183 a0001c0001t0001g0195 others(19): Show |
22 | HG01123.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.474-992T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204563 | |||||||
| chr2:127204566 | A | G | 2 | a0001c0001t0001g0261 a0001c0002t0014g0045 |
2 | NA18962.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.474-995T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204566 | |||||||
| chr2:127204567 | A | G | 8 | a0001c0001t0001g0195 a0001c0001t0001g0250 a0001c0001t0001g0251 others(5): Show |
8 | HG02647.hp1 HG02738.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.474-996T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204567 | |||||||
| chr2:127204571 | A | G | 1 | a0001c0002t0004g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.474-1000T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204571 | |||||||
| chr2:127204575 | A | G | 7 | a0001c0002t0006g0099 a0002c0003t0006g0042 a0002c0003t0010g0037 others(4): Show |
7 | HG02615.hp1 HG02630.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-1004T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204575 | |||||||
| chr2:127204578 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.474-1007T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204578 | |||||||
| chr2:127204579 | A | G | 1 | a0001c0005t0002g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.474-1008T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204579 | |||||||
| chr2:127204582 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.474-1011T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204582 | |||||||
| chr2:127204591 | A | C | 1 | a0001c0001t0002g0146 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.474-1020T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204591 | |||||||
| chr2:127204594 | A | C | 1 | a0001c0001t0001g0026 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.474-1023T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204594 | |||||||
| chr2:127204598 | A | C | 2 | a0001c0001t0001g0026 a0001c0002t0009g0299 |
3 | HG02717.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.474-1027T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204598 | |||||||
| chr2:127204602 | A | AAAGCAAG others(5): Show |
1 | a0001c0001t0038g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.474-1032_474-1031i others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204602 | |||||||
| chr2:127204602 | A | C | 2 | a0001c0001t0001g0026 a0001c0002t0009g0299 |
3 | HG02717.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.474-1031T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204602 | |||||||
| chr2:127204606 | A | C | 3 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 |
4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-1035T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204606 | |||||||
| chr2:127204610 | A | C | 3 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 |
4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-1039T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204610 | |||||||
| chr2:127204614 | A | AAAGAAAG others(5): Show |
1 | a0001c0001t0006g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474-1044_474-1043i others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204614 | |||||||
| chr2:127204619 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.474-1048T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204619 | |||||||
| chr2:127204622 | AAAG | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0183 others(31): Show |
34 | HG00438.hp2 HG00738.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.474-1054_474-1052d others(5): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204622 | |||||||
| chr2:127204623 | A | C | 1 | a0001c0002t0007g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.474-1052T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204623 | |||||||
| chr2:127204625 | G | GA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(93): Show |
115 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.474-1055dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | |||||||
| chr2:127204625 | G | GAAAGA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0185 others(5): Show |
8 | HG00609.hp2 HG00735.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.474-1055_474-1054i others(7): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | |||||||
| chr2:127204625 | G | GAAAGAAA others(2): Show |
6 | a0001c0001t0001g0019 a0001c0001t0001g0186 a0001c0001t0001g0225 others(3): Show |
6 | HG01175.hp1 HG02004.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-1055_474-1054i others(11): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | |||||||
| chr2:127204625 | G | GAAAGAAA others(6): Show |
1 | a0001c0001t0002g0270 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.474-1055_474-1054i others(15): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | |||||||
| chr2:127204625 | G | GAAAGAAA others(10): Show |
3 | a0001c0001t0001g0240 a0001c0002t0015g0301 a0002c0004t0041g0043 |
3 | HG02630.hp2 HG03516.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.474-1055_474-1054i others(19): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | |||||||
| chr2:127204625 | G | GAAAGAAA others(14): Show |
2 | a0002c0003t0006g0042 a0002c0004t0019g0035 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.474-1055_474-1054i others(23): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | |||||||
| chr2:127204625 | G | GAAAGAAA others(18): Show |
1 | a0002c0003t0010g0037 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474-1055_474-1054i others(27): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | |||||||
| chr2:127204626 | A | AC | 12 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0210 others(9): Show |
13 | HG01175.hp2 HG02148.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.474-1056_474-1055i others(3): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204626 | |||||||
| chr2:127204626 | A | C | 5 | a0001c0001t0001g0209 a0001c0001t0025g0208 a0001c0001t0025g0269 others(2): Show |
5 | HG01099.hp1 HG01891.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-1055T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204626 | |||||||
| chr2:127204628 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.474-1057C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204628 | |||||||
| chr2:127204629 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.474-1058T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204629 | |||||||
| chr2:127204722 | G | A | 2 | a0001c0001t0021g0283 a0001c0001t0021g0284 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.474-1151C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204722 | |||||||
| chr2:127204917 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(229): Show |
277 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.473+983A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204917 | |||||||
| chr2:127205059 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(122): Show |
147 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.473+841T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205059 | |||||||
| chr2:127205206 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 |
4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+694C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205206 | |||||||
| chr2:127205238 | C | T | 2 | a0003c0008t0008g0027 a0003c0008t0008g0028 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.473+662G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205238 | |||||||
| chr2:127205282 | C | A | 4 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 others(1): Show |
5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+618G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205282 | |||||||
| chr2:127205344 | G | A | 1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.473+556C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205344 | |||||||
| chr2:127205345 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.473+555C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205345 | |||||||
| chr2:127205428 | T | G | 3 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 |
4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+472A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205428 | |||||||
| chr2:127205520 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 |
4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+380C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205520 | |||||||
| chr2:127205578 | G | A | 1 | a0001c0002t0004g0013 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.473+322C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205578 | |||||||
| chr2:127205692 | C | A | 10 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0209 others(7): Show |
10 | HG01099.hp1 HG01928.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.473+208G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205692 | |||||||
| chr2:127205847 | TC | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(122): Show |
147 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.473+52delG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205847 | |||||||
| chr2:127205897 | C | T | 9 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 others(6): Show |
10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.473+3G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205897 | |||||||
| chr2:127206159 | C | G | 1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-69G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206159 | |||||||
| chr2:127206192 | A | C | 3 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 |
4 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-102T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206192 | |||||||
| chr2:127206199 | T | G | 6 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0007g0290 others(3): Show |
7 | HG02717.hp2 HG02922.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-109A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206199 | |||||||
| chr2:127206290 | CGTTT | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(204): Show |
250 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.283-204_283-201del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206290 | |||||||
| chr2:127206290 | CGTTTGTT others(1): Show |
C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0107 a0001c0001t0038g0300 others(5): Show |
9 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-208_283-201del others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206290 | |||||||
| chr2:127206295 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.283-205C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206295 | |||||||
| chr2:127206307 | G | T | 1 | a0001c0002t0006g0103 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.283-217C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206307 | |||||||
| chr2:127206308 | T | C | 9 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 others(6): Show |
10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-218A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206308 | |||||||
| chr2:127206308 | T | G | 1 | a0001c0002t0006g0103 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.283-218A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206308 | |||||||
| chr2:127206427 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.283-337C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206427 | |||||||
| chr2:127206452 | G | T | 1 | a0001c0001t0002g0021 | 2 | NA19002.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.283-362C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206452 | |||||||
| chr2:127206536 | G | A | 1 | a0001c0001t0008g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.283-446C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206536 | |||||||
| chr2:127206749 | C | T | 2 | a0001c0001t0001g0046 a0001c0002t0009g0092 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.283-659G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206749 | |||||||
| chr2:127206973 | A | G | 21 | a0001c0001t0001g0112 a0001c0001t0002g0089 a0001c0001t0002g0110 others(18): Show |
21 | HG00423.hp1 HG01123.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.283-883T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206973 | |||||||
| chr2:127207048 | T | A | 3 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 |
4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-958A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207048 | |||||||
| chr2:127207056 | C | G | 8 | a0002c0003t0003g0040 a0002c0003t0006g0041 a0002c0003t0006g0042 others(5): Show |
8 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.283-966G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207056 | |||||||
| chr2:127207145 | G | A | 66 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(63): Show |
85 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.283-1055C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207145 | |||||||
| chr2:127207296 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.283-1206T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207296 | |||||||
| chr2:127207408 | C | A | 1 | a0001c0001t0006g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283-1318G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207408 | |||||||
| chr2:127207515 | C | A | 3 | a0001c0001t0002g0007 a0001c0001t0002g0145 a0001c0001t0002g0164 |
5 | HG00280.hp1 HG00733.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-1425G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207515 | |||||||
| chr2:127207660 | ACT | A | 13 | a0002c0003t0003g0040 a0002c0003t0006g0041 a0002c0003t0006g0042 others(10): Show |
15 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.283-1572_283-1571d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207660 | |||||||
| chr2:127207678 | A | T | 73 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(70): Show |
92 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.283-1588T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207678 | |||||||
| chr2:127207680 | AT | A | 22 | a0001c0001t0001g0112 a0001c0001t0001g0253 a0001c0001t0002g0089 others(19): Show |
22 | HG00423.hp1 HG01123.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.283-1591delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207680 | |||||||
| chr2:127207681 | T | A | 3 | a0001c0001t0003g0287 a0001c0001t0008g0288 a0001c0002t0001g0289 |
3 | HG01884.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283-1591A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207681 | |||||||
| chr2:127207818 | A | G | 1 | a0008c0015t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283-1728T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207818 | |||||||
| chr2:127207912 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.283-1822T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207912 | |||||||
| chr2:127208167 | C | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(298): Show |
349 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(346): Show |
intron_variant | MODIFIER | c.283-2077G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208167 | |||||||
| chr2:127208184 | C | A | 3 | a0001c0002t0009g0090 a0001c0002t0009g0091 a0001c0002t0042g0060 |
3 | HG01891.hp1 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-2094G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208184 | |||||||
| chr2:127208235 | A | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(122): Show |
147 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.283-2145T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208235 | |||||||
| chr2:127208269 | A | G | 73 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0001g0133 others(70): Show |
93 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.283-2179T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208269 | |||||||
| chr2:127208295 | C | T | 1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-2205G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208295 | |||||||
| chr2:127208325 | G | A | 1 | a0001c0002t0018g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.283-2235C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208325 | |||||||
| chr2:127208389 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0007g0290 others(2): Show |
6 | HG02717.hp2 HG02922.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-2299G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208389 | |||||||
| chr2:127208519 | C | T | 1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-2429G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208519 | |||||||
| chr2:127208680 | C | A | 3 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 |
4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2590G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208680 | |||||||
| chr2:127208722 | A | C | 1 | a0001c0001t0003g0218 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.283-2632T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208722 | |||||||
| chr2:127208863 | T | G | 1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-2773A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208863 | |||||||
| chr2:127208897 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0121 |
2 | NA18957.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.283-2807G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208897 | |||||||
| chr2:127208902 | C | T | 1 | a0001c0002t0018g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.283-2812G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208902 | |||||||
| chr2:127208917 | CTT | C | 3 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 |
4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2829_283-2828d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208917 | |||||||
| chr2:127209049 | G | A | 2 | a0001c0001t0001g0046 a0001c0002t0009g0092 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.283-2959C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209049 | |||||||
| chr2:127209061 | T | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0003g0050 |
3 | HG02451.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.283-2971A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209061 | |||||||
| chr2:127209116 | C | T | 67 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(64): Show |
86 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.283-3026G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209116 | |||||||
| chr2:127209160 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0038g0300 |
3 | HG02717.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.283-3070A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209160 | |||||||
| chr2:127209178 | C | T | 1 | a0002c0003t0006g0041 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283-3088G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209178 | |||||||
| chr2:127209375 | G | C | 3 | a0001c0001t0003g0287 a0001c0001t0008g0288 a0001c0002t0001g0289 |
3 | HG01884.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283-3285C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209375 | |||||||
| chr2:127209492 | A | G | 1 | a0001c0001t0002g0007 | 3 | HG01255.hp2 HG02486.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.283-3402T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209492 | |||||||
| chr2:127209741 | C | T | 1 | a0008c0015t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283-3651G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209741 | |||||||
| chr2:127209838 | C | T | 4 | a0001c0001t0003g0292 a0001c0002t0015g0291 a0001c0002t0015g0301 others(1): Show |
4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-3748G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209838 | |||||||
| chr2:127209887 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.283-3797G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209887 | |||||||
| chr2:127210042 | T | A | 5 | a0002c0003t0010g0010 a0002c0003t0010g0037 a0002c0003t0010g0039 others(2): Show |
7 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-3952A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210042 | |||||||
| chr2:127210266 | T | G | 2 | a0001c0002t0018g0182 a0001c0002t0018g0211 |
2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.283-4176A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210266 | |||||||
| chr2:127210358 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0002g0255 |
2 | HG00544.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.283-4268C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210358 | |||||||
| chr2:127210432 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.283-4342T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210432 | |||||||
| chr2:127210541 | C | A | 1 | a0001c0001t0002g0270 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.283-4451G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210541 | |||||||
| chr2:127210930 | C | A | 5 | a0001c0001t0002g0014 a0001c0002t0007g0093 a0001c0002t0007g0094 others(2): Show |
6 | HG00639.hp2 HG01081.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-4840G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210930 | |||||||
| chr2:127211081 | G | A | 1 | a0001c0002t0007g0096 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.283-4991C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211081 | |||||||
| chr2:127211088 | A | G | 4 | a0001c0001t0003g0292 a0001c0002t0015g0291 a0001c0002t0015g0301 others(1): Show |
4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-4998T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211088 | |||||||
| chr2:127211127 | G | A | 1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-5037C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211127 | |||||||
| chr2:127211267 | A | AACGACTC others(5): Show |
1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5178_283-5177i others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211267 | |||||||
| chr2:127211286 | A | C | 67 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(64): Show |
86 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.283-5196T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211286 | |||||||
| chr2:127211309 | A | G | 5 | a0002c0003t0010g0010 a0002c0003t0010g0037 a0002c0003t0010g0039 others(2): Show |
7 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-5219T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211309 | |||||||
| chr2:127211361 | G | GTTTTTTT others(4): Show |
1 | a0002c0003t0003g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.283-5272_283-5271i others(13): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | |||||||
| chr2:127211361 | GTTTTTTT others(6): Show |
G | 21 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(18): Show |
23 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.283-5284_283-5272d others(15): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | |||||||
| chr2:127211361 | GTTTTTTT others(7): Show |
G | 44 | a0001c0001t0001g0150 a0001c0001t0002g0003 a0001c0001t0002g0004 others(41): Show |
61 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.283-5285_283-5272d others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | |||||||
| chr2:127211361 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0002g0165 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.283-5286_283-5272d others(17): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | |||||||
| chr2:127211361 | GTTTTTTT others(9): Show |
G | 1 | a0001c0002t0016g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.283-5287_283-5272d others(18): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | |||||||
| chr2:127211361 | GTTTTTTT others(10): Show |
G | 2 | a0001c0002t0016g0295 a0001c0002t0016g0296 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283-5288_283-5272d others(19): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | |||||||
| chr2:127211363 | T | A | 4 | a0001c0001t0003g0292 a0001c0002t0015g0291 a0001c0002t0015g0301 others(1): Show |
4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-5273A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211363 | |||||||
| chr2:127211369 | G | GT | 23 | a0001c0001t0001g0073 a0001c0001t0002g0014 a0001c0001t0002g0110 others(20): Show |
24 | HG00423.hp1 HG01081.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.283-5280dupA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211369 | |||||||
| chr2:127211369 | G | T | 11 | a0001c0001t0005g0188 a0001c0002t0005g0081 a0001c0002t0018g0169 others(8): Show |
11 | HG01123.hp1 HG01243.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-5279C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211369 | |||||||
| chr2:127211369 | GT | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(125): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.283-5280delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211369 | |||||||
| chr2:127211369 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0045g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283-5293_283-5280d others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211369 | |||||||
| chr2:127211369 | GTTTTTTT others(10): Show |
G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0170 a0001c0001t0001g0172 others(2): Show |
6 | HG00735.hp2 HG01168.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-5296_283-5280d others(19): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211369 | |||||||
| chr2:127211370 | T | G | 1 | a0001c0001t0005g0188 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.283-5280A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211370 | |||||||
| chr2:127211376 | T | TG | 4 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 others(1): Show |
5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-5287_283-5286i others(3): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211376 | |||||||
| chr2:127211377 | T | G | 6 | a0001c0001t0001g0107 a0001c0001t0001g0256 a0001c0001t0002g0173 others(3): Show |
6 | HG00544.hp2 HG02040.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-5287A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211377 | |||||||
| chr2:127211378 | T | G | 1 | a0001c0002t0004g0097 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.283-5288A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211378 | |||||||
| chr2:127211380 | T | G | 7 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0264 others(4): Show |
7 | HG00408.hp2 HG00642.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-5290A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211380 | |||||||
| chr2:127211381 | T | G | 8 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-5291A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211381 | |||||||
| chr2:127211382 | T | G | 11 | a0001c0001t0001g0192 a0001c0001t0001g0212 a0001c0001t0001g0214 others(8): Show |
11 | HG01069.hp2 HG01256.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-5292A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211382 | |||||||
| chr2:127211383 | T | G | 1 | a0001c0002t0006g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.283-5293A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211383 | |||||||
| chr2:127211384 | T | G | 4 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 others(1): Show |
5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-5294A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211384 | |||||||
| chr2:127211385 | T | G | 15 | a0001c0001t0001g0216 a0001c0001t0001g0276 a0001c0001t0010g0178 others(12): Show |
16 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.283-5295A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211385 | |||||||
| chr2:127211386 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(114): Show |
138 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.283-5296A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211386 | |||||||
| chr2:127211387 | T | G | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5297A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211387 | |||||||
| chr2:127211389 | T | G | 8 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-5299A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211389 | |||||||
| chr2:127211391 | T | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0276 a0001c0001t0023g0196 |
3 | NA18978.hp2 NA19077.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.283-5301A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211391 | |||||||
| chr2:127211392 | T | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(86): Show |
110 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.283-5302A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211392 | |||||||
| chr2:127211393 | T | G | 8 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-5303A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211393 | |||||||
| chr2:127211395 | T | G | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5305A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211395 | |||||||
| chr2:127211408 | A | C | 3 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 |
4 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-5318T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211408 | |||||||
| chr2:127211408 | A | G | 1 | a0001c0002t0016g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.283-5318T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211408 | |||||||
| chr2:127211454 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.283-5364G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211454 | |||||||
| chr2:127211465 | C | T | 2 | a0001c0001t0002g0116 a0001c0001t0045g0117 |
2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.283-5375G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211465 | |||||||
| chr2:127211484 | G | C | 1 | a0001c0001t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283-5394C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211484 | |||||||
| chr2:127211507 | C | T | 3 | a0001c0002t0007g0290 a0001c0002t0032g0286 a0008c0015t0017g0303 |
3 | HG03453.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-5417G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211507 | |||||||
| chr2:127211555 | T | G | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5465A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211555 | |||||||
| chr2:127211558 | T | G | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5468A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211558 | |||||||
| chr2:127211570 | A | G | 4 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 others(1): Show |
5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-5480T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211570 | |||||||
| chr2:127211593 | G | GCCAGGAT others(8): Show |
1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.283-5518_283-5504d others(17): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211593 | |||||||
| chr2:127211597 | G | A | 67 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(64): Show |
86 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.283-5507C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211597 | |||||||
| chr2:127211753 | T | C | 1 | a0001c0012t0001g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.283-5663A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211753 | |||||||
| chr2:127211892 | A | T | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5802T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211892 | |||||||
| chr2:127211893 | T | G | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5803A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211893 | |||||||
| chr2:127211913 | T | C | 1 | a0001c0002t0018g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.283-5823A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211913 | |||||||
| chr2:127212095 | A | T | 2 | a0001c0002t0032g0286 a0008c0015t0017g0303 |
2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-6005T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212095 | |||||||
| chr2:127212098 | C | A | 4 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 others(1): Show |
5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-6008G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212098 | |||||||
| chr2:127212121 | G | T | 4 | a0003c0006t0017g0030 a0003c0006t0017g0032 a0003c0008t0008g0027 others(1): Show |
4 | HG02109.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-6031C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212121 | |||||||
| chr2:127212186 | A | G | 4 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 others(1): Show |
5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-6096T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212186 | |||||||
| chr2:127212210 | T | C | 4 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 others(1): Show |
5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-6120A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212210 | |||||||
| chr2:127212236 | A | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(122): Show |
147 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.283-6146T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212236 | |||||||
| chr2:127212300 | C | G | 1 | a0001c0002t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283-6210G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212300 | |||||||
| chr2:127212512 | A | C | 4 | a0001c0001t0003g0287 a0001c0001t0008g0288 a0001c0002t0001g0289 others(1): Show |
4 | HG01884.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-6422T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212512 | |||||||
| chr2:127212529 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.283-6439G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212529 | |||||||
| chr2:127212580 | A | G | 1 | a0001c0001t0002g0017 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.283-6490T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212580 | |||||||
| chr2:127212695 | C | A | 1 | a0001c0001t0003g0282 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.283-6605G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212695 | |||||||
| chr2:127212809 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(211): Show |
257 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.283-6719A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212809 | |||||||
| chr2:127212873 | A | T | 1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.283-6783T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212873 | |||||||
| chr2:127212888 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.283-6798G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212888 | |||||||
| chr2:127212902 | T | G | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-6812A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212902 | |||||||
| chr2:127212933 | A | C | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-6843T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212933 | |||||||
| chr2:127212999 | C | T | 1 | a0001c0002t0022g0015 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.283-6909G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212999 | |||||||
| chr2:127213068 | T | G | 1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.282+6921A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213068 | |||||||
| chr2:127213083 | T | A | 1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+6906A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213083 | |||||||
| chr2:127213086 | A | T | 1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+6903T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213086 | |||||||
| chr2:127213143 | A | C | 67 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(64): Show |
86 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.282+6846T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213143 | |||||||
| chr2:127213164 | G | T | 1 | a0001c0001t0048g0130 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.282+6825C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213164 | |||||||
| chr2:127213166 | G | A | 7 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0261 others(4): Show |
7 | NA18947.hp1 NA18950.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+6823C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213166 | |||||||
| chr2:127213292 | T | A | 1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+6697A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213292 | |||||||
| chr2:127213307 | G | GA | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(153): Show |
181 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.282+6681dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213307 | |||||||
| chr2:127213318 | A | AC | 64 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(61): Show |
83 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.282+6670dupG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213318 | |||||||
| chr2:127213318 | A | C | 2 | a0001c0001t0002g0128 a0001c0001t0012g0129 |
2 | NA18947.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.282+6671T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213318 | |||||||
| chr2:127213585 | T | C | 8 | a0002c0003t0003g0040 a0002c0003t0006g0041 a0002c0003t0006g0042 others(5): Show |
8 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.282+6404A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213585 | |||||||
| chr2:127213606 | T | C | 5 | a0001c0002t0006g0058 a0001c0002t0006g0101 a0001c0002t0006g0102 others(2): Show |
5 | HG02015.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+6383A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213606 | |||||||
| chr2:127213649 | T | A | 1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+6340A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213649 | |||||||
| chr2:127213699 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0007g0290 others(4): Show |
8 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+6290C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213699 | |||||||
| chr2:127213704 | A | C | 1 | a0001c0002t0042g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.282+6285T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213704 | |||||||
| chr2:127213724 | C | T | 1 | a0002c0004t0019g0034 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.282+6265G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213724 | |||||||
| chr2:127213963 | A | G | 16 | a0001c0001t0001g0120 a0001c0001t0002g0005 a0001c0001t0002g0016 others(13): Show |
19 | HG00423.hp2 HG00733.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.282+6026T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213963 | |||||||
| chr2:127214014 | C | T | 2 | a0001c0001t0023g0196 a0001c0001t0023g0197 |
2 | HG02015.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.282+5975G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214014 | |||||||
| chr2:127214125 | A | T | 1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+5864T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214125 | |||||||
| chr2:127214126 | C | A | 1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+5863G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214126 | |||||||
| chr2:127214162 | G | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(122): Show |
147 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.282+5827C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214162 | |||||||
| chr2:127214217 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.282+5772C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214217 | |||||||
| chr2:127214237 | A | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(212): Show |
258 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.282+5752T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214237 | |||||||
| chr2:127214358 | A | T | 1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+5631T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214358 | |||||||
| chr2:127214386 | G | A | 8 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+5603C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214386 | |||||||
| chr2:127214467 | C | G | 1 | a0001c0001t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.282+5522G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214467 | |||||||
| chr2:127214542 | A | C | 4 | a0001c0001t0003g0292 a0001c0002t0015g0291 a0001c0002t0015g0301 others(1): Show |
4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+5447T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214542 | |||||||
| chr2:127214652 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(122): Show |
147 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.282+5337A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214652 | |||||||
| chr2:127214678 | T | G | 32 | a0001c0001t0001g0026 a0001c0001t0003g0292 a0001c0001t0021g0283 others(29): Show |
36 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.282+5311A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214678 | |||||||
| chr2:127214736 | C | T | 91 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0001g0133 others(88): Show |
112 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.282+5253G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214736 | |||||||
| chr2:127214780 | T | C | 1 | a0001c0002t0018g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.282+5209A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214780 | |||||||
| chr2:127214782 | G | GT | 34 | a0001c0001t0001g0114 a0001c0001t0001g0177 a0001c0001t0001g0180 others(31): Show |
34 | HG00423.hp1 HG00609.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.282+5206dupA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214782 | |||||||
| chr2:127214782 | G | T | 1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+5207C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214782 | |||||||
| chr2:127214782 | GT | G | 15 | a0001c0001t0002g0116 a0001c0001t0003g0292 a0001c0002t0007g0025 others(12): Show |
16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.282+5206delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214782 | |||||||
| chr2:127214788 | T | G | 4 | a0001c0001t0001g0107 a0001c0002t0007g0104 a0004c0007t0026g0105 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+5201A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214788 | |||||||
| chr2:127214789 | T | G | 69 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(66): Show |
88 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.282+5200A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214789 | |||||||
| chr2:127214790 | T | G | 11 | a0001c0001t0002g0116 a0001c0002t0007g0025 a0001c0002t0007g0297 others(8): Show |
12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.282+5199A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214790 | |||||||
| chr2:127214798 | TTG | T | 68 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0138 others(65): Show |
87 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.282+5189_282+5190d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214798 | |||||||
| chr2:127214799 | T | G | 1 | a0001c0001t0013g0115 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.282+5190A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214799 | |||||||
| chr2:127214800 | G | T | 4 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 others(1): Show |
5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+5189C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214800 | |||||||
| chr2:127214801 | G | T | 2 | a0001c0001t0001g0176 a0001c0001t0003g0175 |
2 | HG02135.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.282+5188C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214801 | |||||||
| chr2:127214802 | T | G | 72 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0001g0133 others(69): Show |
92 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.282+5187A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214802 | |||||||
| chr2:127214851 | G | A | 3 | a0001c0001t0001g0107 a0004c0007t0026g0105 a0004c0007t0027g0106 |
3 | HG02451.hp1 HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.282+5138C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214851 | |||||||
| chr2:127214866 | C | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(227): Show |
275 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.282+5123G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214866 | |||||||
| chr2:127215019 | C | T | 3 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 |
4 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+4970G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215019 | |||||||
| chr2:127215128 | CA | C | 7 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0007g0290 others(4): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+4860delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215128 | |||||||
| chr2:127215128 | CAA | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(221): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.282+4859_282+4860d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215128 | |||||||
| chr2:127215131 | A | C | 1 | a0001c0002t0004g0049 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.282+4858T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215131 | |||||||
| chr2:127215197 | T | C | 2 | a0001c0001t0002g0270 a0001c0001t0002g0274 |
2 | HG02155.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.282+4792A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215197 | |||||||
| chr2:127215243 | T | A | 8 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+4746A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215243 | |||||||
| chr2:127215290 | T | A | 2 | a0001c0001t0002g0168 a0001c0001t0044g0167 |
2 | HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.282+4699A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215290 | |||||||
| chr2:127215383 | G | C | 8 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+4606C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215383 | |||||||
| chr2:127215589 | G | C | 1 | a0001c0001t0001g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+4400C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215589 | |||||||
| chr2:127215627 | T | C | 3 | a0001c0001t0003g0287 a0001c0001t0008g0288 a0001c0002t0001g0289 |
3 | HG01884.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.282+4362A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215627 | |||||||
| chr2:127215739 | G | A | 1 | a0001c0001t0034g0271 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.282+4250C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215739 | |||||||
| chr2:127215779 | A | G | 1 | a0001c0002t0004g0048 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.282+4210T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215779 | |||||||
| chr2:127215783 | G | A | 1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.282+4206C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215783 | |||||||
| chr2:127216044 | T | C | 1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+3945A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216044 | |||||||
| chr2:127216267 | C | T | 1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+3722G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216267 | |||||||
| chr2:127216329 | T | TATAGTCA others(10): Show |
1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+3659_282+3660i others(19): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216329 | |||||||
| chr2:127216345 | A | C | 1 | a0001c0005t0002g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.282+3644T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216345 | |||||||
| chr2:127216529 | G | A | 4 | a0001c0001t0003g0292 a0001c0002t0015g0291 a0001c0002t0015g0301 others(1): Show |
4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+3460C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216529 | |||||||
| chr2:127216626 | G | A | 1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.282+3363C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216626 | |||||||
| chr2:127216792 | A | G | 1 | a0001c0001t0012g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282+3197T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216792 | |||||||
| chr2:127217299 | T | C | 9 | a0001c0002t0007g0025 a0001c0002t0007g0297 a0001c0002t0007g0298 others(6): Show |
10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.282+2690A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217299 | |||||||
| chr2:127217361 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(121): Show |
146 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.282+2628A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217361 | |||||||
| chr2:127217369 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.282+2620C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217369 | |||||||
| chr2:127217393 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0038g0300 a0001c0002t0009g0299 |
4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+2596A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217393 | |||||||
| chr2:127217487 | C | T | 2 | a0001c0001t0021g0283 a0001c0001t0021g0284 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.282+2502G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217487 | |||||||
| chr2:127217548 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.282+2441A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217548 | |||||||
| chr2:127217559 | C | G | 1 | a0001c0001t0002g0173 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.282+2430G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217559 | |||||||
| chr2:127217927 | T | A | 6 | a0003c0006t0017g0030 a0003c0006t0017g0032 a0003c0006t0028g0029 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+2062A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217927 | |||||||
| chr2:127217960 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.282+2029C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217960 | |||||||
| chr2:127217996 | T | C | 1 | a0001c0001t0002g0274 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.282+1993A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217996 | |||||||
| chr2:127218045 | C | A | 82 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0001g0133 others(79): Show |
102 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.282+1944G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218045 | |||||||
| chr2:127218066 | T | C | 1 | a0001c0002t0004g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.282+1923A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218066 | |||||||
| chr2:127218150 | T | A | 1 | a0001c0001t0001g0275 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.282+1839A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218150 | |||||||
| chr2:127218162 | C | T | 4 | a0001c0001t0003g0292 a0001c0002t0015g0291 a0001c0002t0015g0301 others(1): Show |
4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+1827G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218162 | |||||||
| chr2:127218403 | TC | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0170 a0001c0001t0001g0172 others(2): Show |
6 | HG00735.hp2 HG01168.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+1585delG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218403 | |||||||
| chr2:127218463 | T | TG | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0110 others(3): Show |
6 | HG01928.hp2 HG02738.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+1525dupC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218463 | |||||||
| chr2:127218562 | C | A | 2 | a0001c0001t0001g0112 a0001c0001t0002g0113 |
2 | NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.282+1427G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218562 | |||||||
| chr2:127218625 | C | T | 2 | a0003c0008t0008g0027 a0003c0008t0008g0028 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.282+1364G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218625 | |||||||
| chr2:127218798 | A | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(226): Show |
274 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.282+1191T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218798 | |||||||
| chr2:127219241 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(121): Show |
146 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.282+748G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219241 | |||||||
| chr2:127219384 | C | T | 1 | a0001c0002t0007g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.282+605G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219384 | |||||||
| chr2:127219475 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.282+514T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219475 | |||||||
| chr2:127219491 | C | A | 1 | a0008c0015t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.282+498G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219491 | |||||||
| chr2:127219542 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(227): Show |
275 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.282+447A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219542 | |||||||
| chr2:127219595 | C | A | 1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+394G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219595 | |||||||
| chr2:127219707 | C | T | 6 | a0003c0006t0017g0030 a0003c0006t0017g0032 a0003c0006t0028g0029 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+282G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219707 | |||||||
| chr2:127219740 | C | T | 3 | a0001c0001t0003g0287 a0001c0001t0008g0288 a0001c0002t0001g0289 |
3 | HG01884.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.282+249G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219740 | |||||||
| chr2:127219791 | C | T | 1 | a0001c0002t0032g0286 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+198G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219791 | |||||||
| chr2:127219858 | G | A | 5 | a0001c0001t0003g0278 a0001c0001t0003g0279 a0001c0001t0003g0280 others(2): Show |
5 | HG01081.hp2 HG01934.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+131C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219858 | |||||||
| chr2:127219860 | G | A | 2 | a0001c0001t0021g0283 a0001c0001t0021g0284 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.282+129C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219860 | |||||||
| chr2:127219868 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.282+121C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219868 | |||||||
| chr2:127219871 | C | T | 1 | a0001c0002t0014g0045 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.282+118G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219871 | |||||||
| chr2:127219974 | G | A | 19 | a0001c0001t0001g0026 a0001c0001t0003g0287 a0001c0001t0003g0292 others(16): Show |
21 | HG01175.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.282+15C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219974 | |||||||
| chr2:127219974 | G | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(129): Show |
154 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.282+15C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219974 |