Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57597 |
| ensemblid | ENSG00000266074.11 |
| hgncid | 29279 |
| symbol | BAHCC1 |
| name | BAH domain and coiled-coil containing 1 |
| refseq_nuc | NM_001377448.1 |
| refseq_prot | NP_001364377.1 |
| ensembl_nuc | ENST00000675386.2 |
| ensembl_prot | ENSP00000502710.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 81395457 |
| end | 81466331 |
| strand | + |
| ver | v1.2 |
| region | chr17:81395457-81466331 |
| region5000 | chr17:81390457-81471331 |
| regionname0 | BAHCC1_chr17_81395457_81466331 |
| regionname5000 | BAHCC1_chr17_81390457_81471331 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 2608 | 74 | 14 | 6 | 43 | 1 | 9 | 25 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0002 | 0/0 | 2608 | 73 | 17 | 14 | 36 | 4 | 2 | 25 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0003 | 0/0 | 2608 | 46 | 6 | 14 | 21 | 0 | 5 | 13 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0004 | 0/0 | 2608 | 34 | 13 | 13 | 0 | 3 | 5 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0005 | 0/0 | 2608 | 14 | 0 | 2 | 8 | 0 | 4 | 6 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0006 | 0/0 | 2608 | 10 | 2 | 7 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0007 | 0/0 | 2608 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0008 | 0/0 | 2608 | 5 | 0 | 2 | 0 | 0 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0009 | 0/0 | 2608 | 5 | 1 | 0 | 1 | 0 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0010 | 0/0 | 2608 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0011 | 0/0 | 2608 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0012 | 0/0 | 2608 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0013 | 0/0 | 2608 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0014 | 0/0 | 2608 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0015 | 0/0 | 2608 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0016 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0017 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0018 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0019 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0020 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0021 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0022 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0023 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0024 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0025 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0026 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0027 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0028 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0029 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0030 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0031 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0032 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2599): Show |
chr17 | 81390457 | 81471331 |
| a0033 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0034 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0035 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0036 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0037 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0038 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0039 | 0/0 | 2618 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2613): Show |
chr17 | 81390457 | 81471331 |
| a0040 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0041 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0042 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0043 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0044 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0045 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0046 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0047 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0048 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0049 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0050 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0051 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0052 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0053 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0054 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0055 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| a0056 | 0/0 | 2612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2607): Show |
chr17 | 81390457 | 81471331 |
| a0057 | 0/1 | 2608 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | MDGRD others(2603): Show |
chr17 | 81390457 | 81471331 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 7824 | 60 | 13 | 6 | 32 | 1 | 7 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0016 | 0/0 | 7824 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0043 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0051 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0054 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0055 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0056 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0061 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0062 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0071 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0073 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0075 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0001c0080 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0003 | 0/0 | 7824 | 28 | 0 | 4 | 21 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0008 | 0/0 | 7824 | 6 | 3 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0009 | 0/0 | 7824 | 6 | 1 | 2 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0010 | 0/0 | 7824 | 6 | 6 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0012 | 0/0 | 7824 | 5 | 1 | 2 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0019 | 0/0 | 7824 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0021 | 0/0 | 7824 | 3 | 1 | 1 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0025 | 0/0 | 7824 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0026 | 0/0 | 7824 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0032 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0050 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0067 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0068 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0084 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0085 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0091 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0092 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0093 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0099 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0101 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0002c0103 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0003c0002 | 0/0 | 7824 | 42 | 6 | 12 | 19 | 0 | 5 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0003c0018 | 0/0 | 7824 | 3 | 0 | 2 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0003c0063 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0004c0004 | 0/0 | 7824 | 27 | 11 | 11 | 0 | 3 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0004c0011 | 0/0 | 7824 | 5 | 1 | 1 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0004c0035 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0004c0037 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0005c0005 | 0/0 | 7824 | 9 | 0 | 2 | 4 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0005c0028 | 0/0 | 7824 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0005c0064 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0005c0065 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0005c0095 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0006c0006 | 0/0 | 7824 | 7 | 0 | 6 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0006c0020 | 0/0 | 7824 | 3 | 2 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0007c0007 | 0/0 | 7824 | 6 | 5 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0007c0047 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0008c0013 | 0/0 | 7824 | 4 | 0 | 1 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0008c0086 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0009c0024 | 0/0 | 7824 | 2 | 0 | 0 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0009c0029 | 0/0 | 7824 | 2 | 1 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0009c0072 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0010c0014 | 0/0 | 7824 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0011c0017 | 0/0 | 7824 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0012c0031 | 0/0 | 7824 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0012c0102 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0013c0027 | 0/0 | 7824 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0013c0096 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0014c0022 | 0/0 | 7824 | 3 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0015c0015 | 0/0 | 7824 | 3 | 0 | 0 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0016c0039 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0016c0106 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0017c0023 | 0/0 | 7824 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0018c0036 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0018c0105 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0019c0030 | 0/0 | 7824 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0020c0038 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0021c0094 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0022c0034 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0023c0078 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0024c0082 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0025c0066 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0026c0041 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0027c0079 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0028c0044 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0029c0076 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0030c0048 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0031c0098 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0032c0040 | 0/0 | 7812 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7807): Show |
chr17 | 81390457 | 81471331 | ||
| a0033c0088 | 0/0 | 7824 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0034c0069 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0035c0033 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0036c0045 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0037c0089 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0038c0083 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0039c0087 | 0/0 | 7854 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7849): Show |
chr17 | 81390457 | 81471331 | ||
| a0040c0046 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0041c0107 | 0/0 | 7824 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0042c0058 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0043c0053 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0044c0081 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0045c0057 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0046c0052 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0047c0077 | 0/0 | 7824 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0048c0090 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0049c0042 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0050c0059 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0051c0100 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0052c0074 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0053c0070 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0054c0049 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0055c0060 | 0/0 | 7824 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 | ||
| a0056c0104 | 0/0 | 7836 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7831): Show |
chr17 | 81390457 | 81471331 | ||
| a0057c0097 | 0/1 | 7824 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | ATGGA others(7819): Show |
chr17 | 81390457 | 81471331 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10726 | 47 | 13 | 2 | 30 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0001t0002 | 0/0 | 10726 | 6 | 0 | 2 | 1 | 1 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0001t0003 | 1/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0001t0005 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0001t0006 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0001t0007 | 0/0 | 10726 | 2 | 0 | 0 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0001t0018 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0001t0031 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0016t0001 | 0/0 | 10726 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0043t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0051t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0054t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0055t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0056t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0061t0007 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0062t0020 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0071t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0073t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0075t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0001c0080t0001 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0003t0003 | 0/0 | 10726 | 27 | 0 | 3 | 21 | 3 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0003t0010 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0008t0004 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0008t0006 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0008t0024 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0008t0025 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0008t0030 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0008t0037 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0009t0001 | 0/0 | 10726 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0009t0004 | 0/0 | 10726 | 2 | 0 | 2 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0009t0009 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0010t0009 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0010t0015 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0010t0016 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0010t0033 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0012t0002 | 0/0 | 10726 | 5 | 1 | 2 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0019t0003 | 0/0 | 10726 | 3 | 0 | 0 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0021t0002 | 0/0 | 10726 | 3 | 1 | 1 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0025t0003 | 0/0 | 10726 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0026t0003 | 0/0 | 10726 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0032t0003 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0050t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0067t0008 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0068t0007 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0084t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0085t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0091t0004 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0092t0001 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0093t0009 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0099t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0101t0010 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0002c0103t0026 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0003c0002t0001 | 0/0 | 10726 | 24 | 1 | 9 | 14 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0003c0002t0004 | 0/0 | 10726 | 13 | 2 | 2 | 4 | 0 | 5 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0003c0002t0013 | 0/0 | 10726 | 3 | 3 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0003c0002t0028 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0003c0002t0035 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0003c0018t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0003c0018t0002 | 0/0 | 10726 | 2 | 0 | 2 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0003c0063t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0004c0004t0002 | 0/0 | 10726 | 24 | 9 | 11 | 0 | 2 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0004c0004t0014 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0004c0004t0022 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0004c0004t0029 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0004c0011t0002 | 0/0 | 10726 | 3 | 1 | 1 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0004c0011t0004 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0004c0011t0023 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0004c0035t0002 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0004c0037t0014 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0005c0005t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0005c0005t0008 | 0/0 | 10726 | 5 | 0 | 2 | 3 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0005c0005t0012 | 0/0 | 10726 | 3 | 0 | 0 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0005c0028t0001 | 0/0 | 10726 | 2 | 0 | 0 | 2 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0005c0064t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0005c0065t0034 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0005c0095t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0006c0006t0001 | 0/0 | 10726 | 4 | 0 | 3 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0006c0006t0002 | 0/0 | 10726 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0006c0020t0002 | 0/0 | 10726 | 3 | 2 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0007c0007t0001 | 0/0 | 10726 | 5 | 4 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0007c0007t0004 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0007c0047t0002 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0008c0013t0006 | 0/0 | 10726 | 4 | 0 | 1 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0008c0086t0002 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0009c0024t0001 | 0/0 | 10726 | 2 | 0 | 0 | 0 | 0 | 2 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0009c0029t0005 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0009c0029t0021 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0009c0072t0002 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0010c0014t0001 | 0/0 | 10726 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0011c0017t0001 | 0/0 | 10726 | 3 | 0 | 3 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0012c0031t0004 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0012c0102t0004 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0013c0027t0001 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0013c0096t0001 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0014c0022t0011 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0014c0022t0036 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0015c0015t0001 | 0/0 | 10726 | 3 | 0 | 0 | 0 | 0 | 3 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0016c0039t0011 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0016c0106t0010 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0017c0023t0015 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0017c0023t0038 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0018c0036t0001 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0018c0105t0001 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0019c0030t0007 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0020c0038t0002 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0021c0094t0002 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0022c0034t0002 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0023c0078t0003 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0024c0082t0001 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0025c0066t0001 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0026c0041t0019 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0027c0079t0004 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0028c0044t0001 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0029c0076t0001 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0030c0048t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0031c0098t0002 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0032c0040t0002 | 0/0 | 10714 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10709): Show |
chr17 | 81390457 | 81471331 |
| a0033c0088t0001 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0034c0069t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0035c0033t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0036c0045t0004 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0037c0089t0002 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0038c0083t0003 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0039c0087t0004 | 0/0 | 10756 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10751): Show |
chr17 | 81390457 | 81471331 |
| a0040c0046t0027 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0041c0107t0002 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0042c0058t0002 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0043c0053t0001 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0044c0081t0001 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0045c0057t0017 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0046c0052t0001 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0047c0077t0005 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0048c0090t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0049c0042t0004 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0050c0059t0032 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0051c0100t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0052c0074t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0053c0070t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0054c0049t0001 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0055c0060t0003 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| a0056c0104t0010 | 0/0 | 10738 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10733): Show |
chr17 | 81390457 | 81471331 |
| a0057c0097t0002 | 0/1 | 10726 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | GCGCC others(10721): Show |
chr17 | 81390457 | 81471331 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0003g0011 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0018g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0001t0031g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0016t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0016t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0016t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0043t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0051t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0054t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0055t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0056t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0061t0007g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0062t0020g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0071t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0073t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0075t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0001c0080t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0003t0010g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0008t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0008t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0008t0024g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0008t0025g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0008t0030g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0008t0037g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0009t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0009t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0009t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0009t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0009t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0009t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0010t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0010t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0010t0015g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0010t0016g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0010t0016g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0010t0033g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0012t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0012t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0012t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0012t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0012t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0019t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0019t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0019t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0021t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0021t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0021t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0025t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0025t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0026t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0026t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0032t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0050t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0067t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0068t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0084t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0085t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0091t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0092t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0093t0009g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0099t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0101t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0002c0103t0026g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0013g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0028g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0002t0035g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0018t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0018t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0018t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0003c0063t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0014g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0022g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0004t0029g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0011t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0011t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0011t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0011t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0011t0023g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0035t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0004c0037t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0005t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0005t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0005t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0005t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0005t0008g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0005t0008g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0005t0012g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0005t0012g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0005t0012g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0028t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0028t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0064t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0065t0034g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0005c0095t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0006c0006t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0006c0006t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0006c0006t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0006c0006t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0006c0006t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0006c0006t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0006c0006t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0006c0020t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0006c0020t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0006c0020t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0007c0007t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0007c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0007c0007t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0007c0007t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0007c0007t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0007c0007t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0007c0047t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0008c0013t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0008c0013t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0008c0013t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0008c0013t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0008c0086t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0009c0024t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0009c0024t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0009c0029t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0009c0029t0021g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0009c0072t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0010c0014t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0010c0014t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0011c0017t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0011c0017t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0011c0017t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0012c0031t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0012c0031t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0012c0102t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0013c0027t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0013c0027t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0013c0096t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0014c0022t0011g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0014c0022t0011g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0014c0022t0036g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0015c0015t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0015c0015t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0015c0015t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0016c0039t0011g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0016c0106t0010g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0017c0023t0015g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0017c0023t0038g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0018c0036t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0018c0105t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0019c0030t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0019c0030t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0020c0038t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0021c0094t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0022c0034t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0023c0078t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0024c0082t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0025c0066t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0026c0041t0019g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0027c0079t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0028c0044t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0029c0076t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0030c0048t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0031c0098t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0032c0040t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0033c0088t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0034c0069t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0035c0033t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0036c0045t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0037c0089t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0038c0083t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0039c0087t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0040c0046t0027g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0041c0107t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0042c0058t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0043c0053t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0044c0081t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0045c0057t0017g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0046c0052t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0047c0077t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0048c0090t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0049c0042t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0050c0059t0032g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0051c0100t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0052c0074t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0053c0070t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0054c0049t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0055c0060t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0056c0104t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| a0057c0097t0002g0007 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0020 | c0038 | t0002 | g0143 | EUR | GBR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00099 | hp2 | a0002 | c0021 | t0002 | g0088 | EUR | GBR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0141 | EUR | GBR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00140 | hp2 | a0004 | c0004 | t0002 | g0219 | EUR | GBR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00323 | hp1 | a0002 | c0003 | t0003 | g0068 | EUR | FIN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00323 | hp2 | a0004 | c0004 | t0014 | g0190 | EUR | FIN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00408 | hp1 | a0002 | c0003 | t0003 | g0293 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00423 | hp1 | a0001 | c0073 | t0001 | g0055 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00423 | hp2 | a0003 | c0002 | t0001 | g0124 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00438 | hp2 | a0005 | c0005 | t0008 | g0188 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00544 | hp1 | a0002 | c0003 | t0003 | g0304 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00544 | hp2 | a0003 | c0002 | t0004 | g0123 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00609 | hp2 | a0001 | c0043 | t0001 | g0164 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00639 | hp1 | a0010 | c0014 | t0001 | g0243 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00639 | hp2 | a0002 | c0003 | t0003 | g0231 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00642 | hp1 | a0004 | c0004 | t0002 | g0241 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00642 | hp2 | a0003 | c0018 | t0002 | g0144 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00673 | hp1 | a0002 | c0003 | t0003 | g0046 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00673 | hp2 | a0001 | c0055 | t0001 | g0038 | EAS | CHS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00733 | hp1 | a0021 | c0094 | t0002 | g0147 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00733 | hp2 | a0004 | c0004 | t0002 | g0093 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00735 | hp1 | a0004 | c0004 | t0002 | g0158 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00738 | hp1 | a0004 | c0004 | t0002 | g0148 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00738 | hp2 | a0022 | c0034 | t0002 | g0216 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00741 | hp1 | a0003 | c0002 | t0001 | g0101 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG00741 | hp2 | a0004 | c0035 | t0002 | g0215 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01069 | hp1 | a0006 | c0006 | t0002 | g0153 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01069 | hp2 | a0005 | c0005 | t0008 | g0296 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01070 | hp1 | a0002 | c0003 | t0010 | g0211 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01070 | hp2 | a0003 | c0002 | t0001 | g0002 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01071 | hp1 | a0003 | c0002 | t0001 | g0002 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01071 | hp2 | a0006 | c0006 | t0002 | g0154 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01074 | hp1 | a0004 | c0011 | t0002 | g0163 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01074 | hp2 | a0006 | c0020 | t0002 | g0325 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01106 | hp1 | a0004 | c0004 | t0002 | g0092 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01106 | hp2 | a0011 | c0017 | t0001 | g0228 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01109 | hp1 | a0023 | c0078 | t0003 | g0192 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01109 | hp2 | a0003 | c0002 | t0001 | g0100 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01167 | hp1 | a0004 | c0004 | t0002 | g0240 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01167 | hp2 | a0003 | c0002 | t0004 | g0170 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01168 | hp1 | a0004 | c0004 | t0002 | g0010 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01168 | hp2 | a0010 | c0014 | t0001 | g0001 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01169 | hp1 | a0010 | c0014 | t0001 | g0001 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01169 | hp2 | a0003 | c0002 | t0004 | g0171 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01175 | hp1 | a0002 | c0003 | t0003 | g0233 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01175 | hp2 | a0024 | c0082 | t0001 | g0099 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01192 | hp1 | a0004 | c0004 | t0002 | g0167 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01192 | hp2 | a0008 | c0013 | t0006 | g0072 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01243 | hp1 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01243 | hp2 | a0007 | c0007 | t0001 | g0309 | AMR | PUR | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01255 | hp1 | a0004 | c0004 | t0002 | g0266 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01255 | hp2 | a0002 | c0008 | t0004 | g0117 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01261 | hp1 | a0002 | c0008 | t0006 | g0134 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01261 | hp2 | a0002 | c0008 | t0025 | g0253 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01346 | hp1 | a0011 | c0017 | t0001 | g0180 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01346 | hp2 | a0002 | c0012 | t0002 | g0159 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01358 | hp1 | a0001 | c0001 | t0031 | g0196 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01358 | hp2 | a0006 | c0006 | t0001 | g0150 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01361 | hp1 | a0003 | c0018 | t0002 | g0210 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01433 | hp1 | a0003 | c0002 | t0001 | g0098 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01433 | hp2 | a0025 | c0066 | t0001 | g0305 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01496 | hp1 | a0002 | c0021 | t0002 | g0114 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01515 | hp1 | a0002 | c0003 | t0003 | g0186 | EUR | IBS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01515 | hp2 | a0026 | c0041 | t0019 | g0013 | EUR | IBS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01516 | hp1 | a0027 | c0079 | t0004 | g0128 | EUR | IBS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01516 | hp2 | a0002 | c0003 | t0003 | g0184 | EUR | IBS | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01884 | hp2 | a0028 | c0044 | t0001 | g0249 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01891 | hp1 | a0007 | c0007 | t0001 | g0021 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01891 | hp2 | a0004 | c0004 | t0002 | g0270 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01928 | hp1 | a0003 | c0002 | t0001 | g0106 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01928 | hp2 | a0008 | c0086 | t0002 | g0091 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01934 | hp1 | a0005 | c0005 | t0008 | g0297 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01934 | hp2 | a0004 | c0004 | t0002 | g0218 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01943 | hp1 | a0002 | c0091 | t0004 | g0227 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01943 | hp2 | a0002 | c0003 | t0003 | g0067 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01952 | hp1 | a0003 | c0002 | t0001 | g0107 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01975 | hp1 | a0011 | c0017 | t0001 | g0299 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01975 | hp2 | a0029 | c0076 | t0001 | g0094 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01978 | hp1 | a0006 | c0006 | t0002 | g0155 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01978 | hp2 | a0002 | c0009 | t0004 | g0121 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01981 | hp1 | a0002 | c0032 | t0003 | g0232 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01981 | hp2 | a0003 | c0002 | t0001 | g0074 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02004 | hp1 | a0002 | c0009 | t0004 | g0301 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02004 | hp2 | a0003 | c0002 | t0001 | g0111 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02015 | hp1 | a0002 | c0009 | t0001 | g0079 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02015 | hp2 | a0002 | c0025 | t0003 | g0212 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02027 | hp2 | a0003 | c0002 | t0001 | g0057 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02055 | hp1 | a0002 | c0008 | t0030 | g0264 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02055 | hp2 | a0004 | c0037 | t0014 | g0256 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02056 | hp2 | a0030 | c0048 | t0003 | g0076 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02071 | hp2 | a0003 | c0002 | t0001 | g0183 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02074 | hp1 | a0003 | c0002 | t0001 | g0103 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02074 | hp2 | a0002 | c0099 | t0003 | g0051 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02080 | hp1 | a0002 | c0003 | t0003 | g0050 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02080 | hp2 | a0003 | c0002 | t0001 | g0213 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02083 | hp1 | a0002 | c0050 | t0001 | g0288 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02083 | hp2 | a0005 | c0028 | t0001 | g0073 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02129 | hp2 | a0001 | c0016 | t0001 | g0316 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02132 | hp1 | a0002 | c0003 | t0003 | g0302 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02132 | hp2 | a0003 | c0002 | t0035 | g0197 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02135 | hp1 | a0001 | c0016 | t0001 | g0181 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02155 | hp1 | a0001 | c0001 | t0018 | g0040 | EAS | CDX | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02155 | hp2 | a0002 | c0003 | t0003 | g0047 | EAS | CDX | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02165 | hp1 | a0009 | c0029 | t0005 | g0066 | EAS | CDX | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02257 | hp2 | a0003 | c0002 | t0013 | g0173 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02258 | hp1 | a0032 | c0040 | t0002 | g0268 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02258 | hp2 | a0012 | c0102 | t0004 | g0017 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02273 | hp1 | a0003 | c0002 | t0028 | g0298 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02273 | hp2 | a0006 | c0006 | t0001 | g0151 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02280 | hp2 | a0004 | c0004 | t0002 | g0003 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0149 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02300 | hp2 | a0033 | c0088 | t0001 | g0261 | AMR | PEL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02451 | hp1 | a0002 | c0068 | t0007 | g0254 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02451 | hp2 | a0002 | c0012 | t0002 | g0058 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02523 | hp1 | a0034 | c0069 | t0003 | g0116 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02523 | hp2 | a0035 | c0033 | t0001 | g0179 | EAS | KHV | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02615 | hp1 | a0002 | c0103 | t0026 | g0245 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02615 | hp2 | a0013 | c0096 | t0001 | g0235 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02622 | hp1 | a0002 | c0009 | t0009 | g0185 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02630 | hp2 | a0002 | c0010 | t0016 | g0161 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02647 | hp1 | a0013 | c0027 | t0001 | g0024 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02647 | hp2 | a0014 | c0022 | t0011 | g0322 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02683 | hp1 | a0009 | c0072 | t0002 | g0193 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02698 | hp1 | a0001 | c0080 | t0001 | g0043 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02698 | hp2 | a0004 | c0004 | t0002 | g0127 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02717 | hp1 | a0036 | c0045 | t0004 | g0273 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02717 | hp2 | a0017 | c0023 | t0015 | g0277 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02723 | hp1 | a0014 | c0022 | t0011 | g0323 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02735 | hp1 | a0015 | c0015 | t0001 | g0118 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02735 | hp2 | a0004 | c0011 | t0002 | g0120 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02738 | hp1 | a0003 | c0002 | t0004 | g0194 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02738 | hp2 | a0004 | c0011 | t0023 | g0041 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02809 | hp1 | a0001 | c0062 | t0020 | g0252 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02809 | hp2 | a0007 | c0007 | t0001 | g0312 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02818 | hp1 | a0018 | c0036 | t0001 | g0019 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02818 | hp2 | a0002 | c0010 | t0033 | g0135 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02886 | hp2 | a0003 | c0002 | t0013 | g0168 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02895 | hp1 | a0003 | c0002 | t0004 | g0172 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02895 | hp2 | a0012 | c0031 | t0004 | g0016 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02922 | hp2 | a0007 | c0047 | t0002 | g0308 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02965 | hp2 | a0007 | c0007 | t0001 | g0257 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02976 | hp2 | a0017 | c0023 | t0038 | g0027 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0090 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03098 | hp1 | a0002 | c0021 | t0002 | g0262 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03098 | hp2 | a0004 | c0004 | t0002 | g0272 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03130 | hp1 | a0002 | c0010 | t0009 | g0260 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03130 | hp2 | a0004 | c0011 | t0002 | g0023 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03139 | hp2 | a0019 | c0030 | t0007 | g0032 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03195 | hp1 | a0007 | c0007 | t0001 | g0005 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03195 | hp2 | a0004 | c0004 | t0022 | g0139 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03209 | hp1 | a0037 | c0089 | t0002 | g0265 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03209 | hp2 | a0004 | c0004 | t0002 | g0269 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03239 | hp2 | a0005 | c0005 | t0012 | g0204 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03453 | hp1 | a0009 | c0029 | t0021 | g0311 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03453 | hp2 | a0004 | c0004 | t0002 | g0222 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03486 | hp1 | a0002 | c0010 | t0009 | g0014 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03486 | hp2 | a0003 | c0002 | t0004 | g0310 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03490 | hp1 | a0008 | c0013 | t0006 | g0029 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03490 | hp2 | a0038 | c0083 | t0003 | g0129 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03491 | hp1 | a0005 | c0005 | t0012 | g0206 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03491 | hp2 | a0039 | c0087 | t0004 | g0165 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03492 | hp1 | a0005 | c0005 | t0012 | g0207 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03492 | hp2 | a0008 | c0013 | t0006 | g0140 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03516 | hp1 | a0040 | c0046 | t0027 | g0263 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03516 | hp2 | a0003 | c0002 | t0013 | g0025 | AFR | ESN | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03540 | hp1 | a0006 | c0020 | t0002 | g0022 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03540 | hp2 | a0002 | c0101 | t0010 | g0020 | AFR | GWD | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03579 | hp1 | a0002 | c0093 | t0009 | g0015 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03579 | hp2 | a0041 | c0107 | t0002 | g0251 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0064 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03654 | hp2 | a0042 | c0058 | t0002 | g0008 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03669 | hp1 | a0008 | c0013 | t0006 | g0162 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03669 | hp2 | a0015 | c0015 | t0001 | g0119 | SAS | PJL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03831 | hp2 | a0009 | c0024 | t0001 | g0175 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03834 | hp1 | a0004 | c0011 | t0004 | g0071 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03834 | hp2 | a0043 | c0053 | t0001 | g0126 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03927 | hp1 | a0044 | c0081 | t0001 | g0236 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03927 | hp2 | a0004 | c0004 | t0002 | g0061 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03942 | hp1 | a0003 | c0002 | t0004 | g0205 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03942 | hp2 | a0005 | c0065 | t0034 | g0313 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG04115 | hp1 | a0002 | c0012 | t0002 | g0112 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0145 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG04184 | hp1 | a0003 | c0002 | t0004 | g0182 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG04184 | hp2 | a0002 | c0012 | t0002 | g0133 | SAS | BEB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG04199 | hp1 | a0045 | c0057 | t0017 | g0191 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG04199 | hp2 | a0046 | c0052 | t0001 | g0195 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG04204 | hp1 | a0047 | c0077 | t0005 | g0063 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG04204 | hp2 | a0009 | c0024 | t0001 | g0306 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG04228 | hp1 | a0003 | c0002 | t0004 | g0229 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG04228 | hp2 | a0001 | c0061 | t0007 | g0152 | SAS | STU | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18612 | hp1 | a0003 | c0002 | t0004 | g0280 | EAS | CHB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18612 | hp2 | a0048 | c0090 | t0001 | g0042 | EAS | CHB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18747 | hp2 | a0002 | c0003 | t0003 | g0080 | EAS | CHB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18906 | hp1 | a0004 | c0004 | t0002 | g0156 | AFR | YRI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18942 | hp1 | a0003 | c0002 | t0004 | g0295 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18942 | hp2 | a0002 | c0085 | t0003 | g0031 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18944 | hp1 | a0003 | c0002 | t0001 | g0062 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18944 | hp2 | a0005 | c0028 | t0001 | g0226 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18947 | hp1 | a0002 | c0003 | t0003 | g0110 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18948 | hp1 | a0003 | c0002 | t0001 | g0096 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18948 | hp2 | a0005 | c0005 | t0008 | g0085 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18950 | hp1 | a0002 | c0026 | t0003 | g0247 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18951 | hp1 | a0005 | c0064 | t0005 | g0178 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18951 | hp2 | a0002 | c0003 | t0003 | g0053 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18952 | hp2 | a0002 | c0003 | t0003 | g0300 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18962 | hp1 | a0002 | c0003 | t0003 | g0259 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18962 | hp2 | a0001 | c0075 | t0001 | g0303 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18963 | hp1 | a0002 | c0003 | t0003 | g0290 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18963 | hp2 | a0005 | c0095 | t0005 | g0199 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18964 | hp2 | a0049 | c0042 | t0004 | g0060 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18966 | hp1 | a0003 | c0063 | t0005 | g0198 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18966 | hp2 | a0003 | c0002 | t0001 | g0095 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18967 | hp1 | a0002 | c0026 | t0003 | g0246 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18967 | hp2 | a0003 | c0002 | t0001 | g0104 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18969 | hp1 | a0050 | c0059 | t0032 | g0125 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18969 | hp2 | a0051 | c0100 | t0001 | g0237 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18970 | hp1 | a0052 | c0074 | t0001 | g0082 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18970 | hp2 | a0002 | c0019 | t0003 | g0294 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18971 | hp1 | a0002 | c0009 | t0001 | g0034 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18975 | hp2 | a0002 | c0003 | t0003 | g0230 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18977 | hp1 | a0002 | c0003 | t0003 | g0258 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18977 | hp2 | a0002 | c0009 | t0001 | g0255 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18980 | hp1 | a0053 | c0070 | t0003 | g0006 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18980 | hp2 | a0003 | c0018 | t0001 | g0307 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18981 | hp2 | a0054 | c0049 | t0001 | g0102 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18983 | hp1 | a0002 | c0019 | t0003 | g0315 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18983 | hp2 | a0002 | c0019 | t0003 | g0200 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18984 | hp1 | a0003 | c0002 | t0001 | g0209 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18984 | hp2 | a0002 | c0003 | t0003 | g0059 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18986 | hp2 | a0055 | c0060 | t0003 | g0189 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18990 | hp1 | a0002 | c0067 | t0008 | g0069 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA18990 | hp2 | a0003 | c0002 | t0001 | g0039 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19002 | hp1 | a0002 | c0003 | t0003 | g0208 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19005 | hp1 | a0003 | c0002 | t0001 | g0056 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19007 | hp1 | a0002 | c0003 | t0003 | g0044 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19007 | hp2 | a0003 | c0002 | t0004 | g0122 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19009 | hp2 | a0001 | c0054 | t0005 | g0283 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19010 | hp1 | a0002 | c0003 | t0003 | g0314 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19010 | hp2 | a0001 | c0071 | t0001 | g0077 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19011 | hp1 | a0005 | c0005 | t0008 | g0087 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19011 | hp2 | a0003 | c0002 | t0001 | g0105 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19012 | hp2 | a0001 | c0056 | t0003 | g0284 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19030 | hp1 | a0019 | c0030 | t0007 | g0239 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19030 | hp2 | a0004 | c0004 | t0002 | g0221 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19043 | hp1 | a0007 | c0007 | t0004 | g0317 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19043 | hp2 | a0002 | c0010 | t0015 | g0275 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19060 | hp1 | a0002 | c0003 | t0003 | g0289 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19060 | hp2 | a0002 | c0025 | t0003 | g0065 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19066 | hp2 | a0005 | c0005 | t0005 | g0202 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19080 | hp1 | a0002 | c0084 | t0001 | g0070 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19080 | hp2 | a0002 | c0003 | t0003 | g0048 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19082 | hp1 | a0001 | c0016 | t0001 | g0052 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19082 | hp2 | a0001 | c0051 | t0001 | g0045 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19083 | hp2 | a0002 | c0003 | t0003 | g0286 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19085 | hp1 | a0003 | c0002 | t0001 | g0049 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19240 | hp1 | a0016 | c0039 | t0011 | g0271 | AFR | YRI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA19240 | hp2 | a0004 | c0004 | t0002 | g0138 | AFR | YRI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA20129 | hp1 | a0014 | c0022 | t0036 | g0318 | AFR | ASW | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ASW | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA20805 | hp1 | a0004 | c0004 | t0002 | g0214 | EUR | TSI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA20805 | hp2 | a0006 | c0006 | t0001 | g0201 | EUR | TSI | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA20905 | hp1 | a0015 | c0015 | t0001 | g0166 | SAS | GIH | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA20905 | hp2 | a0003 | c0002 | t0004 | g0115 | SAS | GIH | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01123 | hp1 | a0002 | c0012 | t0002 | g0137 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG01123 | hp2 | a0006 | c0006 | t0001 | g0009 | AMR | CLM | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02109 | hp1 | a0002 | c0010 | t0016 | g0234 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02109 | hp2 | a0031 | c0098 | t0002 | g0267 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02486 | hp1 | a0016 | c0106 | t0010 | g0328 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02486 | hp2 | a0004 | c0004 | t0002 | g0217 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02559 | hp1 | a0006 | c0020 | t0002 | g0238 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG02559 | hp2 | a0013 | c0027 | t0001 | g0026 | AFR | ACB | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03471 | hp1 | a0002 | c0008 | t0037 | g0319 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG03471 | hp2 | a0004 | c0004 | t0029 | g0220 | AFR | MSL | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG06807 | hp1 | a0002 | c0092 | t0001 | g0146 | AFR | USA | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| HG06807 | hp2 | a0002 | c0008 | t0024 | g0248 | AFR | USA | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA20300 | hp1 | a0018 | c0105 | t0001 | g0250 | AFR | USA | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA20300 | hp2 | a0003 | c0002 | t0001 | g0097 | AFR | USA | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA21309 | hp1 | a0012 | c0031 | t0004 | g0018 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| NA21309 | hp2 | a0056 | c0104 | t0010 | g0160 | AFR | LWK | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| homoSapiens | chm13v2 | a0057 | c0097 | t0002 | g0007 | REF | REF | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0011 | REF | REF | BAHCC1_chr17_81390457_81471331 | BAHCC1 | chr17 | 81390457 | 81471331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81399839 | G | GGGCCCGC others(5): Show |
1 | a0056 | 1 | NA21309.hp2 | disruptive_inframe_insertion | MODERATE | c.101_112dupGGCCCGCC others(4): Show |
p.Ala37_Gln38insArgP others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/28 | 498/10726 | 113/7827 | 38/2608 | INFO_REALIGN_3_PRIME | chr17 | 81399839 | ||
| chr17:81441921 | A | C | 1 | a0051 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.572A>C | p.His191Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 957/10726 | 572/7827 | 191/2608 | chr17 | 81441921 | |||
| chr17:81441922 | C | A | 1 | a0051 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.573C>A | p.His191Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 958/10726 | 573/7827 | 191/2608 | chr17 | 81441922 | |||
| chr17:81442163 | G | A | 8 | a0004 a0010 a0016 others(5): Show |
45 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(42): Show |
missense_variant | MODERATE | c.814G>A | p.Ala272Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1199/10726 | 814/7827 | 272/2608 | chr17 | 81442163 | |||
| chr17:81442301 | G | A | 1 | a0049 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.952G>A | p.Gly318Arg | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1337/10726 | 952/7827 | 318/2608 | chr17 | 81442301 | |||
| chr17:81442391 | G | A | 2 | a0014 a0031 |
4 | HG02109.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
missense_variant | MODERATE | c.1042G>A | p.Ala348Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1427/10726 | 1042/7827 | 348/2608 | chr17 | 81442391 | |||
| chr17:81442400 | G | A | 1 | a0022 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.1051G>A | p.Ala351Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1436/10726 | 1051/7827 | 351/2608 | chr17 | 81442400 | |||
| chr17:81442403 | G | A | 3 | a0028 a0036 a0040 |
3 | HG01884.hp2 HG02717.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.1054G>A | p.Gly352Arg | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1439/10726 | 1054/7827 | 352/2608 | chr17 | 81442403 | |||
| chr17:81442580 | G | A | 1 | a0007 | 7 | HG01243.hp2 HG01891.hp1 HG02809.hp2 others(4): Show |
missense_variant | MODERATE | c.1231G>A | p.Ala411Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1616/10726 | 1231/7827 | 411/2608 | chr17 | 81442580 | |||
| chr17:81442616 | C | T | 1 | a0027 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1267C>T | p.Arg423Trp | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1652/10726 | 1267/7827 | 423/2608 | chr17 | 81442616 | |||
| chr17:81442617 | G | A | 1 | a0030 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.1268G>A | p.Arg423Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1653/10726 | 1268/7827 | 423/2608 | chr17 | 81442617 | |||
| chr17:81443549 | G | A | 1 | a0054 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.2200G>A | p.Ala734Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 2585/10726 | 2200/7827 | 734/2608 | chr17 | 81443549 | |||
| chr17:81443902 | G | T | 1 | a0023 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.2309G>T | p.Arg770Leu | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/28 | 2694/10726 | 2309/7827 | 770/2608 | chr17 | 81443902 | |||
| chr17:81444486 | C | A | 2 | a0008 a0013 |
8 | HG01192.hp2 HG01928.hp2 HG02559.hp2 others(5): Show |
missense_variant | MODERATE | c.2430C>A | p.Asp810Glu | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 7/28 | 2815/10726 | 2430/7827 | 810/2608 | chr17 | 81444486 | |||
| chr17:81444552 | G | T | 1 | a0047 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.2496G>T | p.Met832Ile | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 7/28 | 2881/10726 | 2496/7827 | 832/2608 | chr17 | 81444552 | |||
| chr17:81444796 | C | T | 1 | a0029 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.2641C>T | p.Pro881Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 8/28 | 3026/10726 | 2641/7827 | 881/2608 | chr17 | 81444796 | |||
| chr17:81445060 | G | T | 1 | a0052 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.2717G>T | p.Gly906Val | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 9/28 | 3102/10726 | 2717/7827 | 906/2608 | chr17 | 81445060 | |||
| chr17:81445439 | C | A | 2 | a0006 a0031 |
11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
missense_variant | MODERATE | c.2921C>A | p.Thr974Asn | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3306/10726 | 2921/7827 | 974/2608 | chr17 | 81445439 | |||
| chr17:81445525 | G | A | 1 | a0046 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.3007G>A | p.Ala1003Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3392/10726 | 3007/7827 | 1003/2608 | chr17 | 81445525 | |||
| chr17:81447057 | G | A | 1 | a0056 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.3185G>A | p.Arg1062His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 3570/10726 | 3185/7827 | 1062/2608 | chr17 | 81447057 | |||
| chr17:81447281 | A | G | 35 | a0002 a0003 a0004 others(32): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
missense_variant | MODERATE | c.3409A>G | p.Thr1137Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 3794/10726 | 3409/7827 | 1137/2608 | chr17 | 81447281 | |||
| chr17:81447417 | G | A | 1 | a0015 | 3 | HG02735.hp1 HG03669.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.3545G>A | p.Arg1182Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 3930/10726 | 3545/7827 | 1182/2608 | chr17 | 81447417 | |||
| chr17:81447608 | G | A | 2 | a0006 a0031 |
11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
missense_variant | MODERATE | c.3736G>A | p.Gly1246Arg | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 4121/10726 | 3736/7827 | 1246/2608 | chr17 | 81447608 | |||
| chr17:81447639 | C | T | 1 | a0021 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.3767C>T | p.Ala1256Val | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 4152/10726 | 3767/7827 | 1256/2608 | chr17 | 81447639 | |||
| chr17:81447737 | C | A | 1 | a0043 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.3865C>A | p.Pro1289Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 4250/10726 | 3865/7827 | 1289/2608 | chr17 | 81447737 | |||
| chr17:81451999 | G | A | 11 | a0003 a0004 a0016 others(8): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
missense_variant | MODERATE | c.4208G>A | p.Arg1403Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/28 | 4593/10726 | 4208/7827 | 1403/2608 | chr17 | 81451999 | |||
| chr17:81452835 | G | A | 1 | a0028 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.4429G>A | p.Asp1477Asn | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/28 | 4814/10726 | 4429/7827 | 1477/2608 | chr17 | 81452835 | |||
| chr17:81455361 | G | A | 2 | a0005 a0033 |
15 | HG00438.hp2 HG01069.hp2 HG01934.hp1 others(12): Show |
missense_variant | MODERATE | c.4540G>A | p.Val1514Ile | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/28 | 4925/10726 | 4540/7827 | 1514/2608 | chr17 | 81455361 | |||
| chr17:81455365 | A | G | 1 | a0034 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.4544A>G | p.Tyr1515Cys | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/28 | 4929/10726 | 4544/7827 | 1515/2608 | chr17 | 81455365 | |||
| chr17:81455368 | C | T | 1 | a0035 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.4547C>T | p.Ala1516Val | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/28 | 4932/10726 | 4547/7827 | 1516/2608 | chr17 | 81455368 | |||
| chr17:81456347 | CGTGGCCC others(5): Show |
C | 1 | a0032 | 1 | HG02258.hp1 | disruptive_inframe_deletion | MODERATE | c.4629_4640delCAGGGT others(6): Show |
p.His1543_Ala1546del | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/28 | 5014/10726 | 4629/7827 | 1543/2608 | INFO_REALIGN_3_PRIME | chr17 | 81456347 | ||
| chr17:81456525 | G | A | 1 | a0051 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.4798G>A | p.Gly1600Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/28 | 5183/10726 | 4798/7827 | 1600/2608 | chr17 | 81456525 | |||
| chr17:81457490 | A | G | 34 | a0002 a0003 a0004 others(31): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
missense_variant | MODERATE | c.4939A>G | p.Thr1647Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/28 | 5324/10726 | 4939/7827 | 1647/2608 | chr17 | 81457490 | |||
| chr17:81458372 | G | A | 1 | a0012 | 3 | HG02258.hp2 HG02895.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.5249G>A | p.Arg1750Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/28 | 5634/10726 | 5249/7827 | 1750/2608 | chr17 | 81458372 | |||
| chr17:81458411 | G | A | 1 | a0050 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.5288G>A | p.Ser1763Asn | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/28 | 5673/10726 | 5288/7827 | 1763/2608 | chr17 | 81458411 | |||
| chr17:81458443 | A | C | 1 | a0038 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.5320A>C | p.Thr1774Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/28 | 5705/10726 | 5320/7827 | 1774/2608 | chr17 | 81458443 | |||
| chr17:81458645 | A | G | 2 | a0012 a0019 |
5 | HG02258.hp2 HG02895.hp2 HG03139.hp2 others(2): Show |
missense_variant | MODERATE | c.5368A>G | p.Thr1790Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 19/28 | 5753/10726 | 5368/7827 | 1790/2608 | chr17 | 81458645 | |||
| chr17:81459285 | A | G | 1 | a0024 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.5753A>G | p.Asn1918Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/28 | 6138/10726 | 5753/7827 | 1918/2608 | chr17 | 81459285 | |||
| chr17:81460363 | G | A | 2 | a0037 a0042 |
2 | HG03209.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.5992G>A | p.Val1998Ile | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 24/28 | 6377/10726 | 5992/7827 | 1998/2608 | chr17 | 81460363 | |||
| chr17:81460920 | A | G | 2 | a0016 a0017 |
4 | HG02486.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.6257A>G | p.His2086Arg | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6642/10726 | 6257/7827 | 2086/2608 | chr17 | 81460920 | |||
| chr17:81460932 | G | A | 1 | a0044 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.6269G>A | p.Arg2090His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6654/10726 | 6269/7827 | 2090/2608 | chr17 | 81460932 | |||
| chr17:81460935 | G | A | 2 | a0041 a0048 |
2 | HG03579.hp2 NA18612.hp2 |
missense_variant | MODERATE | c.6272G>A | p.Arg2091His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6657/10726 | 6272/7827 | 2091/2608 | chr17 | 81460935 | |||
| chr17:81460961 | G | A | 1 | a0025 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.6298G>A | p.Ala2100Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6683/10726 | 6298/7827 | 2100/2608 | chr17 | 81460961 | |||
| chr17:81461093 | G | A | 1 | a0053 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.6430G>A | p.Val2144Met | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6815/10726 | 6430/7827 | 2144/2608 | chr17 | 81461093 | |||
| chr17:81461336 | G | T | 1 | a0045 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.6673G>T | p.Ala2225Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 7058/10726 | 6673/7827 | 2225/2608 | chr17 | 81461336 | |||
| chr17:81461793 | G | A | 1 | a0040 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.7130G>A | p.Arg2377His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 7515/10726 | 7130/7827 | 2377/2608 | chr17 | 81461793 | |||
| chr17:81462870 | G | A | 1 | a0020 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.7514G>A | p.Arg2505His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/28 | 7899/10726 | 7514/7827 | 2505/2608 | chr17 | 81462870 | |||
| chr17:81463711 | G | A | 4 | a0011 a0029 a0033 others(1): Show |
6 | HG01106.hp2 HG01346.hp1 HG01975.hp1 others(3): Show |
missense_variant | MODERATE | c.7721G>A | p.Arg2574Gln | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 8106/10726 | 7721/7827 | 2574/2608 | chr17 | 81463711 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81399811 | C | T | 3 | a0016c0106 a0018c0105 a0041c0107 |
3 | HG02486.hp1 HG03579.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.72C>T | p.Ala24Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/28 | 457/10726 | 72/7827 | 24/2608 | chr17 | 81399811 | |||
| chr17:81399895 | G | A | 1 | a0002c0032 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.156G>A | p.Pro52Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/28 | 541/10726 | 156/7827 | 52/2608 | chr17 | 81399895 | |||
| chr17:81426873 | G | A | 1 | a0035c0033 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.252G>A | p.Ser84Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/28 | 637/10726 | 252/7827 | 84/2608 | chr17 | 81426873 | |||
| chr17:81426891 | C | G | 1 | a0002c0103 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.270C>G | p.Pro90Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/28 | 655/10726 | 270/7827 | 90/2608 | chr17 | 81426891 | |||
| chr17:81441898 | C | T | 3 | a0002c0101 a0012c0031 a0012c0102 |
4 | HG02258.hp2 HG02895.hp2 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.549C>T | p.Ser183Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 934/10726 | 549/7827 | 183/2608 | chr17 | 81441898 | |||
| chr17:81441994 | C | T | 1 | a0002c0099 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.645C>T | p.Phe215Phe | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1030/10726 | 645/7827 | 215/2608 | chr17 | 81441994 | |||
| chr17:81442264 | C | T | 2 | a0014c0022 a0031c0098 |
4 | HG02109.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
synonymous_variant | LOW | c.915C>T | p.Gly305Gly | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1300/10726 | 915/7827 | 305/2608 | chr17 | 81442264 | |||
| chr17:81442345 | G | A | 1 | a0001c0043 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.996G>A | p.Pro332Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1381/10726 | 996/7827 | 332/2608 | chr17 | 81442345 | |||
| chr17:81442348 | C | T | 1 | a0013c0096 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.999C>T | p.Ala333Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1384/10726 | 999/7827 | 333/2608 | chr17 | 81442348 | |||
| chr17:81442408 | A | C | 1 | a0004c0035 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.1059A>C | p.Pro353Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1444/10726 | 1059/7827 | 353/2608 | chr17 | 81442408 | |||
| chr17:81442408 | A | G | 50 | a0002c0010 a0002c0021 a0002c0025 others(47): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
synonymous_variant | LOW | c.1059A>G | p.Pro353Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1444/10726 | 1059/7827 | 353/2608 | chr17 | 81442408 | |||
| chr17:81442502 | C | A | 1 | a0017c0023 | 2 | HG02717.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.1153C>A | p.Arg385Arg | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1538/10726 | 1153/7827 | 385/2608 | chr17 | 81442502 | |||
| chr17:81442588 | C | T | 1 | a0001c0080 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1239C>T | p.Ala413Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1624/10726 | 1239/7827 | 413/2608 | chr17 | 81442588 | |||
| chr17:81442684 | G | A | 12 | a0004c0004 a0004c0035 a0004c0037 others(9): Show |
40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
synonymous_variant | LOW | c.1335G>A | p.Lys445Lys | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 1720/10726 | 1335/7827 | 445/2608 | chr17 | 81442684 | |||
| chr17:81443164 | C | T | 1 | a0026c0041 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.1815C>T | p.Tyr605Tyr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 2200/10726 | 1815/7827 | 605/2608 | chr17 | 81443164 | |||
| chr17:81443230 | G | A | 10 | a0002c0025 a0002c0026 a0002c0084 others(7): Show |
54 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(51): Show |
synonymous_variant | LOW | c.1881G>A | p.Pro627Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 2266/10726 | 1881/7827 | 627/2608 | chr17 | 81443230 | |||
| chr17:81443518 | C | T | 1 | a0012c0102 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.2169C>T | p.Tyr723Tyr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/28 | 2554/10726 | 2169/7827 | 723/2608 | chr17 | 81443518 | |||
| chr17:81444798 | C | G | 1 | a0001c0075 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.2643C>G | p.Pro881Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 8/28 | 3028/10726 | 2643/7827 | 881/2608 | chr17 | 81444798 | |||
| chr17:81445091 | G | A | 1 | a0002c0050 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.2748G>A | p.Pro916Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 9/28 | 3133/10726 | 2748/7827 | 916/2608 | chr17 | 81445091 | |||
| chr17:81445380 | T | C | 1 | a0001c0051 | 1 | NA19082.hp2 | synonymous_variant | LOW | c.2862T>C | p.Asp954Asp | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3247/10726 | 2862/7827 | 954/2608 | chr17 | 81445380 | |||
| chr17:81445392 | C | T | 1 | a0001c0073 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.2874C>T | p.Pro958Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3259/10726 | 2874/7827 | 958/2608 | chr17 | 81445392 | |||
| chr17:81445440 | C | T | 1 | a0009c0072 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.2922C>T | p.Thr974Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3307/10726 | 2922/7827 | 974/2608 | chr17 | 81445440 | |||
| chr17:81445452 | G | A | 2 | a0013c0027 a0013c0096 |
3 | HG02559.hp2 HG02615.hp2 HG02647.hp1 |
synonymous_variant | LOW | c.2934G>A | p.Pro978Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3319/10726 | 2934/7827 | 978/2608 | chr17 | 81445452 | |||
| chr17:81445461 | C | T | 1 | a0005c0095 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.2943C>T | p.Pro981Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3328/10726 | 2943/7827 | 981/2608 | chr17 | 81445461 | |||
| chr17:81445524 | C | T | 1 | a0001c0071 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.3006C>T | p.Pro1002Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3391/10726 | 3006/7827 | 1002/2608 | chr17 | 81445524 | |||
| chr17:81445536 | C | G | 2 | a0002c0019 a0053c0070 |
4 | NA18970.hp2 NA18980.hp1 NA18983.hp1 others(1): Show |
synonymous_variant | LOW | c.3018C>G | p.Pro1006Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3403/10726 | 3018/7827 | 1006/2608 | chr17 | 81445536 | |||
| chr17:81445563 | G | A | 1 | a0051c0100 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.3045G>A | p.Pro1015Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3430/10726 | 3045/7827 | 1015/2608 | chr17 | 81445563 | |||
| chr17:81445596 | C | T | 1 | a0002c0026 | 2 | NA18950.hp1 NA18967.hp1 |
synonymous_variant | LOW | c.3078C>T | p.Pro1026Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/28 | 3463/10726 | 3078/7827 | 1026/2608 | chr17 | 81445596 | |||
| chr17:81447295 | C | T | 3 | a0001c0062 a0018c0105 a0056c0104 |
3 | HG02809.hp1 NA20300.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.3423C>T | p.Pro1141Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 3808/10726 | 3423/7827 | 1141/2608 | chr17 | 81447295 | |||
| chr17:81447769 | A | G | 1 | a0002c0093 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.3897A>G | p.Ser1299Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 4282/10726 | 3897/7827 | 1299/2608 | chr17 | 81447769 | |||
| chr17:81447778 | T | C | 3 | a0006c0006 a0006c0020 a0031c0098 |
11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
synonymous_variant | LOW | c.3906T>C | p.His1302His | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/28 | 4291/10726 | 3906/7827 | 1302/2608 | chr17 | 81447778 | |||
| chr17:81451726 | C | T | 1 | a0001c0061 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.4035C>T | p.Ala1345Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 12/28 | 4420/10726 | 4035/7827 | 1345/2608 | chr17 | 81451726 | |||
| chr17:81451744 | C | T | 25 | a0002c0003 a0002c0009 a0002c0019 others(22): Show |
61 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(58): Show |
synonymous_variant | LOW | c.4053C>T | p.Ala1351Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 12/28 | 4438/10726 | 4053/7827 | 1351/2608 | chr17 | 81451744 | |||
| chr17:81457462 | A | G | 1 | a0002c0092 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.4911A>G | p.Pro1637Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/28 | 5296/10726 | 4911/7827 | 1637/2608 | chr17 | 81457462 | |||
| chr17:81457492 | C | T | 1 | a0005c0028 | 2 | HG02083.hp2 NA18944.hp2 |
synonymous_variant | LOW | c.4941C>T | p.Thr1647Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/28 | 5326/10726 | 4941/7827 | 1647/2608 | chr17 | 81457492 | |||
| chr17:81457511 | C | T | 19 | a0002c0084 a0003c0002 a0003c0018 others(16): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
synonymous_variant | LOW | c.4960C>T | p.Leu1654Leu | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/28 | 5345/10726 | 4960/7827 | 1654/2608 | chr17 | 81457511 | |||
| chr17:81457564 | G | A | 1 | a0004c0037 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.5013G>A | p.Lys1671Lys | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/28 | 5398/10726 | 5013/7827 | 1671/2608 | chr17 | 81457564 | |||
| chr17:81458295 | C | T | 2 | a0002c0019 a0053c0070 |
4 | NA18970.hp2 NA18980.hp1 NA18983.hp1 others(1): Show |
synonymous_variant | LOW | c.5172C>T | p.Ala1724Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/28 | 5557/10726 | 5172/7827 | 1724/2608 | chr17 | 81458295 | |||
| chr17:81458959 | C | T | 1 | a0042c0058 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.5595C>T | p.Ser1865Ser | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 20/28 | 5980/10726 | 5595/7827 | 1865/2608 | chr17 | 81458959 | |||
| chr17:81459154 | G | T | 1 | a0002c0085 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.5706G>T | p.Leu1902Leu | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 21/28 | 6091/10726 | 5706/7827 | 1902/2608 | chr17 | 81459154 | |||
| chr17:81460329 | C | T | 1 | a0002c0068 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.5958C>T | p.Asp1986Asp | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 24/28 | 6343/10726 | 5958/7827 | 1986/2608 | chr17 | 81460329 | |||
| chr17:81460341 | A | C | 2 | a0012c0031 a0012c0102 |
3 | HG02258.hp2 HG02895.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.5970A>C | p.Thr1990Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 24/28 | 6355/10726 | 5970/7827 | 1990/2608 | chr17 | 81460341 | |||
| chr17:81460906 | G | A | 1 | a0001c0016 | 3 | HG02129.hp2 HG02135.hp1 NA19082.hp1 |
synonymous_variant | LOW | c.6243G>A | p.Thr2081Thr | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 6628/10726 | 6243/7827 | 2081/2608 | chr17 | 81460906 | |||
| chr17:81461389 | C | T | 1 | a0002c0092 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.6726C>T | p.Pro2242Pro | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 7111/10726 | 6726/7827 | 2242/2608 | chr17 | 81461389 | |||
| chr17:81461572 | G | A | 6 | a0001c0054 a0002c0067 a0003c0063 others(3): Show |
14 | HG00438.hp2 HG01069.hp2 HG01934.hp1 others(11): Show |
synonymous_variant | LOW | c.6909G>A | p.Ala2303Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 7294/10726 | 6909/7827 | 2303/2608 | chr17 | 81461572 | |||
| chr17:81461575 | C | T | 9 | a0002c0012 a0002c0021 a0006c0020 others(6): Show |
19 | HG00099.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
synonymous_variant | LOW | c.6912C>T | p.Ala2304Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/28 | 7297/10726 | 6912/7827 | 2304/2608 | chr17 | 81461575 | |||
| chr17:81462769 | G | A | 1 | a0001c0055 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.7413G>A | p.Lys2471Lys | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/28 | 7798/10726 | 7413/7827 | 2471/2608 | chr17 | 81462769 | |||
| chr17:81462826 | C | T | 19 | a0001c0056 a0002c0003 a0002c0019 others(16): Show |
50 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
synonymous_variant | LOW | c.7470C>T | p.Ala2490Ala | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/28 | 7855/10726 | 7470/7827 | 2490/2608 | chr17 | 81462826 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81399639 | C | T | 1 | a0017c0023t0038 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/28 | 101 | chr17 | 81399639 | ||||||
| chr17:81399674 | A | G | 2 | a0002c0008t0037 a0014c0022t0036 |
2 | HG03471.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-66A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/28 | 66 | chr17 | 81399674 | ||||||
| chr17:81463822 | C | A | 1 | a0045c0057t0017 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 5 | chr17 | 81463822 | ||||||
| chr17:81463852 | G | A | 3 | a0002c0009t0009 a0002c0010t0009 a0002c0093t0009 |
4 | HG02622.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*35G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 35 | chr17 | 81463852 | ||||||
| chr17:81463865 | G | A | 1 | a0001c0001t0018 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*48G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 48 | chr17 | 81463865 | ||||||
| chr17:81464292 | G | A | 6 | a0001c0001t0006 a0001c0062t0020 a0002c0008t0006 others(3): Show |
9 | HG01192.hp2 HG01261.hp1 HG01515.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*475G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 475 | chr17 | 81464292 | ||||||
| chr17:81464405 | C | T | 1 | a0003c0002t0013 | 3 | HG02257.hp2 HG02886.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*588C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 588 | chr17 | 81464405 | ||||||
| chr17:81464733 | A | G | 1 | a0003c0002t0035 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*916A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 916 | chr17 | 81464733 | ||||||
| chr17:81464817 | G | A | 30 | a0001c0001t0002 a0001c0001t0007 a0001c0061t0007 others(27): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1000G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1000 | chr17 | 81464817 | ||||||
| chr17:81464817 | G | C | 1 | a0004c0011t0023 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1000G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1000 | chr17 | 81464817 | ||||||
| chr17:81464977 | G | A | 7 | a0001c0001t0006 a0001c0062t0020 a0002c0008t0006 others(4): Show |
10 | HG01192.hp2 HG01261.hp1 HG01261.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1160G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1160 | chr17 | 81464977 | ||||||
| chr17:81465013 | C | T | 1 | a0004c0004t0022 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1196C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1196 | chr17 | 81465013 | ||||||
| chr17:81465074 | C | T | 1 | a0005c0065t0034 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1257C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1257 | chr17 | 81465074 | ||||||
| chr17:81465176 | T | C | 59 | a0001c0001t0002 a0001c0001t0006 a0001c0062t0020 others(56): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1359T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1359 | chr17 | 81465176 | ||||||
| chr17:81465237 | A | C | 3 | a0002c0009t0009 a0002c0010t0009 a0002c0093t0009 |
4 | HG02622.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1420A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1420 | chr17 | 81465237 | ||||||
| chr17:81465325 | C | T | 15 | a0001c0001t0005 a0001c0054t0005 a0002c0008t0025 others(12): Show |
22 | HG00438.hp2 HG01069.hp2 HG01261.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1508C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1508 | chr17 | 81465325 | ||||||
| chr17:81465370 | C | T | 2 | a0002c0067t0008 a0005c0005t0008 |
6 | HG00438.hp2 HG01069.hp2 HG01934.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1553C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1553 | chr17 | 81465370 | ||||||
| chr17:81465375 | C | T | 19 | a0002c0008t0004 a0002c0008t0030 a0002c0008t0037 others(16): Show |
36 | HG00544.hp2 HG01167.hp2 HG01169.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1558C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1558 | chr17 | 81465375 | ||||||
| chr17:81465403 | G | A | 54 | a0001c0001t0002 a0001c0001t0006 a0002c0008t0004 others(51): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1586G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1586 | chr17 | 81465403 | ||||||
| chr17:81465569 | G | T | 2 | a0002c0008t0030 a0002c0008t0037 |
2 | HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1752G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1752 | chr17 | 81465569 | ||||||
| chr17:81465645 | T | C | 116 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(113): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*1828T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1828 | chr17 | 81465645 | ||||||
| chr17:81465671 | C | A | 1 | a0001c0001t0031 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1854C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1854 | chr17 | 81465671 | ||||||
| chr17:81465810 | G | A | 1 | a0009c0029t0021 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1993G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 1993 | chr17 | 81465810 | ||||||
| chr17:81466037 | C | A | 1 | a0002c0103t0026 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2220C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 2220 | chr17 | 81466037 | ||||||
| chr17:81466055 | C | T | 1 | a0002c0010t0033 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2238C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 2238 | chr17 | 81466055 | ||||||
| chr17:81466080 | C | T | 120 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(117): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*2263C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 2263 | chr17 | 81466080 | ||||||
| chr17:81466103 | G | A | 1 | a0026c0041t0019 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2286G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 2286 | chr17 | 81466103 | ||||||
| chr17:81466134 | G | A | 2 | a0040c0046t0027 a0045c0057t0017 |
2 | HG03516.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2317G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 28/28 | 2317 | chr17 | 81466134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81395658 | A | AT | 202 | a0001c0001t0001g0004 a0001c0001t0001g0131 a0001c0001t0001g0136 others(199): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-207+33dupT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81395658 | ||||||
| chr17:81395807 | C | CT | 91 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0035 others(88): Show |
91 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-207+182dupT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81395807 | ||||||
| chr17:81395807 | C | CTT | 179 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0075 others(176): Show |
182 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-207+181_-207+182d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81395807 | ||||||
| chr17:81395996 | C | G | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-207+361C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81395996 | |||||||
| chr17:81396027 | A | C | 304 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(301): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-207+392A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396027 | |||||||
| chr17:81396110 | C | G | 1 | a0027c0079t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-207+475C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396110 | |||||||
| chr17:81396200 | T | G | 1 | a0001c0055t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-207+565T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396200 | |||||||
| chr17:81396293 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-207+658T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396293 | |||||||
| chr17:81396457 | C | G | 32 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(29): Show |
32 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.-207+822C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396457 | |||||||
| chr17:81396532 | G | A | 1 | a0007c0007t0001g0005 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-207+897G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396532 | |||||||
| chr17:81396615 | C | T | 1 | a0004c0004t0002g0127 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-207+980C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396615 | |||||||
| chr17:81396707 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-207+1072A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396707 | |||||||
| chr17:81396722 | C | G | 1 | a0027c0079t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-207+1087C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396722 | |||||||
| chr17:81396854 | C | A | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-207+1219C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396854 | |||||||
| chr17:81396861 | C | G | 1 | a0016c0106t0010g0328 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-207+1226C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396861 | |||||||
| chr17:81396868 | C | T | 1 | a0056c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-207+1233C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396868 | |||||||
| chr17:81396894 | C | T | 6 | a0001c0001t0001g0324 a0001c0001t0001g0326 a0001c0001t0001g0327 others(3): Show |
6 | HG01074.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-207+1259C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396894 | |||||||
| chr17:81396900 | C | G | 319 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(316): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-207+1265C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396900 | |||||||
| chr17:81396952 | C | A | 1 | a0002c0010t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-207+1317C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81396952 | |||||||
| chr17:81397039 | G | A | 2 | a0002c0026t0003g0246 a0002c0026t0003g0247 |
2 | NA18950.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-207+1404G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397039 | |||||||
| chr17:81397090 | C | T | 1 | a0027c0079t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-207+1455C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397090 | |||||||
| chr17:81397275 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-207+1640C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397275 | |||||||
| chr17:81397296 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-207+1661G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397296 | |||||||
| chr17:81397393 | G | A | 8 | a0001c0062t0020g0252 a0002c0008t0024g0248 a0002c0008t0025g0253 others(5): Show |
8 | HG01261.hp2 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-207+1758G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397393 | |||||||
| chr17:81397395 | G | A | 8 | a0001c0062t0020g0252 a0002c0008t0024g0248 a0002c0008t0025g0253 others(5): Show |
8 | HG01261.hp2 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-207+1760G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397395 | |||||||
| chr17:81397395 | G | GA | 28 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-207+1777dupA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81397395 | ||||||
| chr17:81397407 | A | C | 1 | a0001c0001t0001g0321 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-207+1772A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397407 | |||||||
| chr17:81397410 | A | AC | 19 | a0001c0001t0001g0030 a0001c0043t0001g0164 a0001c0062t0020g0252 others(16): Show |
19 | HG00609.hp2 HG01074.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-207+1775_-207+177 others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397410 | |||||||
| chr17:81397410 | A | C | 254 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0033 others(251): Show |
257 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.-207+1775A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397410 | |||||||
| chr17:81397414 | A | C | 4 | a0004c0004t0002g0167 a0004c0004t0002g0240 a0004c0004t0002g0241 others(1): Show |
4 | HG00642.hp1 HG01167.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-207+1779A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397414 | |||||||
| chr17:81397430 | C | T | 5 | a0001c0001t0001g0030 a0001c0043t0001g0164 a0002c0085t0003g0031 others(2): Show |
5 | HG00609.hp2 HG03491.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-207+1795C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397430 | |||||||
| chr17:81397525 | T | A | 1 | a0003c0002t0001g0039 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-207+1890T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397525 | |||||||
| chr17:81397537 | A | T | 1 | a0050c0059t0032g0125 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-207+1902A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397537 | |||||||
| chr17:81397623 | G | A | 31 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-206-1911G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397623 | |||||||
| chr17:81397638 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-206-1896C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397638 | |||||||
| chr17:81397912 | G | A | 1 | a0002c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-206-1622G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81397912 | |||||||
| chr17:81398035 | A | T | 1 | a0004c0004t0002g0156 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-206-1499A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398035 | |||||||
| chr17:81398208 | T | G | 1 | a0001c0001t0018g0040 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-206-1326T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398208 | |||||||
| chr17:81398486 | GCCGCCCG others(3): Show |
G | 11 | a0001c0001t0001g0320 a0001c0062t0020g0252 a0002c0008t0024g0248 others(8): Show |
11 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-206-1046_-206-103 others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81398486 | ||||||
| chr17:81398525 | C | T | 1 | a0002c0010t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-206-1009C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398525 | |||||||
| chr17:81398606 | AC | A | 170 | a0001c0001t0001g0030 a0001c0001t0001g0131 a0001c0001t0001g0136 others(167): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-206-920delC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81398606 | ||||||
| chr17:81398613 | C | A | 6 | a0001c0001t0001g0169 a0003c0002t0004g0170 a0003c0002t0004g0171 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-206-921C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398613 | |||||||
| chr17:81398613 | C | G | 3 | a0003c0002t0001g0124 a0003c0002t0004g0122 a0003c0002t0004g0123 |
3 | HG00423.hp2 HG00544.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-206-921C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398613 | |||||||
| chr17:81398614 | CA | C | 3 | a0007c0007t0001g0257 a0007c0007t0004g0317 a0019c0030t0007g0239 |
3 | HG02965.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-206-919delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398614 | |||||||
| chr17:81398689 | C | T | 30 | a0001c0001t0001g0136 a0001c0001t0001g0142 a0001c0001t0001g0157 others(27): Show |
30 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-206-845C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398689 | |||||||
| chr17:81398772 | CGGGCCTC others(2): Show |
C | 172 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0033 others(169): Show |
175 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.-206-757_-206-749d others(11): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81398772 | ||||||
| chr17:81398819 | C | G | 1 | a0002c0009t0004g0121 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-206-715C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398819 | |||||||
| chr17:81398825 | A | G | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-206-709A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398825 | |||||||
| chr17:81398933 | T | TA | 16 | a0001c0001t0001g0174 a0002c0008t0030g0264 a0002c0010t0016g0161 others(13): Show |
17 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-206-587dupA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81398933 | ||||||
| chr17:81398974 | C | G | 1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-206-560C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81398974 | |||||||
| chr17:81399011 | G | T | 1 | a0001c0016t0001g0316 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-206-523G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399011 | |||||||
| chr17:81399110 | G | A | 3 | a0004c0004t0002g0167 a0004c0004t0002g0240 a0004c0004t0002g0241 |
3 | HG00642.hp1 HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-206-424G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399110 | |||||||
| chr17:81399128 | A | AGT | 25 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0281 others(22): Show |
25 | HG00609.hp2 HG00741.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-206-382_-206-381d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | ||||||
| chr17:81399128 | A | AGTGT | 146 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-206-384_-206-381d others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | ||||||
| chr17:81399128 | A | AGTGTGT | 25 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(22): Show |
25 | HG00423.hp2 HG00639.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-206-386_-206-381d others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | ||||||
| chr17:81399128 | A | AGTGTGTG others(1): Show |
10 | a0004c0004t0002g0003 a0004c0004t0002g0269 a0004c0004t0002g0270 others(7): Show |
11 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-206-388_-206-381d others(10): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | ||||||
| chr17:81399128 | A | AGTGTGTG others(3): Show |
1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-206-390_-206-381d others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | ||||||
| chr17:81399128 | A | AGTGTGTG others(5): Show |
2 | a0001c0001t0001g0276 a0017c0023t0015g0277 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-206-392_-206-381d others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | ||||||
| chr17:81399128 | AGTGT | A | 5 | a0003c0002t0004g0205 a0005c0005t0012g0204 a0005c0005t0012g0206 others(2): Show |
5 | HG03239.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-206-384_-206-381d others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | ||||||
| chr17:81399128 | AGTGTGT | A | 42 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0001t0001g0176 others(39): Show |
42 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.-206-386_-206-381d others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399128 | ||||||
| chr17:81399152 | T | C | 2 | a0001c0001t0002g0132 a0002c0008t0024g0248 |
2 | HG03017.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-206-382T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399152 | |||||||
| chr17:81399152 | T | TGC | 41 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(38): Show |
41 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-206-380_-206-379d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr17 | 81399152 | ||||||
| chr17:81399220 | C | A | 1 | a0001c0001t0001g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-206-314C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399220 | |||||||
| chr17:81399241 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-206-293A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399241 | |||||||
| chr17:81399244 | C | T | 1 | a0005c0065t0034g0313 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-206-290C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399244 | |||||||
| chr17:81399289 | C | T | 2 | a0007c0007t0001g0257 a0007c0007t0004g0317 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-206-245C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399289 | |||||||
| chr17:81399297 | C | A | 1 | a0001c0001t0002g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-206-237C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399297 | |||||||
| chr17:81399315 | C | T | 1 | a0002c0003t0010g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-206-219C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399315 | |||||||
| chr17:81399342 | C | A | 40 | a0001c0001t0001g0244 a0001c0001t0001g0278 a0001c0001t0001g0279 others(37): Show |
40 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.-206-192C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399342 | |||||||
| chr17:81399371 | G | A | 1 | a0002c0003t0003g0044 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-206-163G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399371 | |||||||
| chr17:81399403 | C | A | 222 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(219): Show |
225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-206-131C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399403 | |||||||
| chr17:81399441 | G | A | 1 | a0002c0099t0003g0051 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-206-93G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 1/27 | chr17 | 81399441 | |||||||
| chr17:81399985 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.178+68C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81399985 | |||||||
| chr17:81399991 | C | T | 7 | a0001c0001t0001g0131 a0001c0061t0007g0152 a0006c0006t0001g0150 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+74C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81399991 | |||||||
| chr17:81400083 | A | G | 11 | a0001c0001t0001g0320 a0001c0062t0020g0252 a0002c0008t0024g0248 others(8): Show |
11 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+166A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400083 | |||||||
| chr17:81400162 | G | A | 171 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0033 others(168): Show |
174 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.178+245G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400162 | |||||||
| chr17:81400181 | C | G | 1 | a0056c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.178+264C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400181 | |||||||
| chr17:81400218 | C | A | 1 | a0002c0012t0002g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.178+301C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400218 | |||||||
| chr17:81400385 | C | A | 2 | a0001c0001t0001g0276 a0017c0023t0015g0277 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.178+468C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400385 | |||||||
| chr17:81400407 | G | A | 5 | a0002c0093t0009g0015 a0012c0031t0004g0016 a0012c0031t0004g0018 others(2): Show |
5 | HG02258.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+490G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400407 | |||||||
| chr17:81400412 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG00438.hp1 NA18747.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.178+495A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400412 | |||||||
| chr17:81400444 | T | TA | 19 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(16): Show |
19 | HG00639.hp2 HG00738.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.178+530dupA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81400444 | ||||||
| chr17:81400479 | C | T | 1 | a0004c0011t0002g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.178+562C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400479 | |||||||
| chr17:81400541 | G | A | 11 | a0001c0001t0001g0244 a0001c0001t0001g0278 a0001c0001t0001g0287 others(8): Show |
11 | HG02083.hp1 NA18963.hp1 NA18975.hp1 others(8): Show |
intron_variant | MODIFIER | c.178+624G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400541 | |||||||
| chr17:81400566 | G | A | 2 | a0004c0004t0002g0214 a0004c0004t0002g0217 |
2 | HG02486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.178+649G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400566 | |||||||
| chr17:81400570 | A | T | 1 | a0019c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178+653A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400570 | |||||||
| chr17:81400581 | G | A | 1 | a0001c0016t0001g0052 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.178+664G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400581 | |||||||
| chr17:81400589 | G | A | 1 | a0006c0006t0001g0009 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.178+672G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400589 | |||||||
| chr17:81400594 | G | A | 3 | a0001c0001t0001g0054 a0001c0073t0001g0055 a0002c0003t0003g0053 |
3 | HG00423.hp1 NA18951.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.178+677G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400594 | |||||||
| chr17:81400729 | C | T | 1 | a0028c0044t0001g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.178+812C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81400729 | |||||||
| chr17:81401308 | G | C | 2 | a0003c0002t0001g0056 a0003c0002t0001g0057 |
2 | HG02027.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.178+1391G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401308 | |||||||
| chr17:81401337 | T | C | 1 | a0001c0001t0002g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.178+1420T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401337 | |||||||
| chr17:81401391 | C | T | 1 | a0004c0004t0002g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.178+1474C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401391 | |||||||
| chr17:81401515 | C | T | 32 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(29): Show |
32 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.178+1598C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401515 | |||||||
| chr17:81401560 | G | A | 172 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0033 others(169): Show |
175 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.178+1643G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401560 | |||||||
| chr17:81401724 | A | G | 1 | a0002c0009t0001g0034 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.178+1807A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401724 | |||||||
| chr17:81401741 | T | G | 1 | a0002c0008t0006g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.178+1824T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401741 | |||||||
| chr17:81401746 | C | A | 1 | a0002c0012t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.178+1829C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401746 | |||||||
| chr17:81401825 | A | ACT | 123 | a0001c0001t0001g0030 a0001c0001t0001g0131 a0001c0001t0001g0136 others(120): Show |
123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.178+1912_178+1913d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81401825 | ||||||
| chr17:81401887 | C | T | 33 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.178+1970C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81401887 | |||||||
| chr17:81402131 | C | T | 2 | a0005c0005t0005g0202 a0017c0023t0038g0027 |
2 | HG02976.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.178+2214C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402131 | |||||||
| chr17:81402198 | C | A | 31 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.178+2281C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402198 | |||||||
| chr17:81402226 | C | T | 1 | a0002c0003t0003g0304 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.178+2309C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402226 | |||||||
| chr17:81402300 | G | A | 1 | a0002c0003t0003g0059 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.178+2383G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402300 | |||||||
| chr17:81402322 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.178+2405G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402322 | |||||||
| chr17:81402483 | C | T | 1 | a0002c0012t0002g0159 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.178+2566C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402483 | |||||||
| chr17:81402568 | G | C | 1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.178+2651G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402568 | |||||||
| chr17:81402623 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0291 |
2 | NA19009.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.178+2706G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402623 | |||||||
| chr17:81402787 | C | T | 1 | a0015c0015t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.178+2870C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402787 | |||||||
| chr17:81402820 | G | A | 11 | a0001c0001t0001g0320 a0001c0062t0020g0252 a0002c0008t0024g0248 others(8): Show |
11 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+2903G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402820 | |||||||
| chr17:81402902 | G | C | 1 | a0001c0001t0001g0279 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.178+2985G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81402902 | |||||||
| chr17:81403072 | A | C | 8 | a0001c0001t0001g0004 a0002c0021t0002g0114 a0003c0002t0004g0310 others(5): Show |
9 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.178+3155A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403072 | |||||||
| chr17:81403148 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.178+3231G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403148 | |||||||
| chr17:81403156 | G | A | 1 | a0009c0024t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.178+3239G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403156 | |||||||
| chr17:81403196 | C | G | 2 | a0001c0001t0001g0326 a0001c0001t0001g0327 |
2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.178+3279C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403196 | |||||||
| chr17:81403196 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.178+3279C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403196 | |||||||
| chr17:81403197 | G | A | 3 | a0002c0008t0030g0264 a0002c0021t0002g0262 a0040c0046t0027g0263 |
3 | HG02055.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178+3280G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403197 | |||||||
| chr17:81403219 | G | C | 1 | a0001c0001t0001g0176 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.178+3302G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403219 | |||||||
| chr17:81403246 | C | T | 31 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.178+3329C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403246 | |||||||
| chr17:81403401 | A | T | 174 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0033 others(171): Show |
177 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.178+3484A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403401 | |||||||
| chr17:81403456 | A | G | 31 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.178+3539A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403456 | |||||||
| chr17:81403481 | CA | C | 253 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0033 others(250): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.178+3577delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81403481 | ||||||
| chr17:81403481 | CAA | C | 40 | a0001c0001t0001g0030 a0001c0001t0001g0223 a0001c0001t0001g0224 others(37): Show |
40 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.178+3576_178+3577d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81403481 | ||||||
| chr17:81403501 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.178+3584G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403501 | |||||||
| chr17:81403546 | A | G | 1 | a0003c0002t0013g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.178+3629A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403546 | |||||||
| chr17:81403671 | C | T | 2 | a0005c0005t0012g0206 a0005c0005t0012g0207 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.178+3754C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403671 | |||||||
| chr17:81403736 | C | T | 1 | a0003c0002t0004g0205 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.178+3819C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403736 | |||||||
| chr17:81403743 | C | T | 1 | a0043c0053t0001g0126 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.178+3826C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403743 | |||||||
| chr17:81403744 | G | A | 1 | a0003c0002t0001g0039 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.178+3827G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403744 | |||||||
| chr17:81403786 | C | G | 91 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0035 others(88): Show |
92 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.178+3869C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403786 | |||||||
| chr17:81403786 | C | T | 46 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0001t0001g0176 others(43): Show |
46 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.178+3869C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403786 | |||||||
| chr17:81403947 | C | T | 1 | a0002c0003t0010g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.178+4030C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403947 | |||||||
| chr17:81403967 | A | G | 1 | a0002c0068t0007g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.178+4050A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81403967 | |||||||
| chr17:81404038 | C | T | 4 | a0001c0001t0001g0131 a0006c0006t0002g0153 a0006c0006t0002g0154 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+4121C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404038 | |||||||
| chr17:81404410 | T | C | 1 | a0019c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178+4493T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404410 | |||||||
| chr17:81404424 | C | T | 31 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.178+4507C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404424 | |||||||
| chr17:81404751 | C | G | 174 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0033 others(171): Show |
177 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.178+4834C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404751 | |||||||
| chr17:81404792 | C | T | 1 | a0002c0003t0003g0044 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.178+4875C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404792 | |||||||
| chr17:81404793 | G | A | 31 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0142 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.178+4876G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81404793 | |||||||
| chr17:81405065 | T | C | 1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.178+5148T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405065 | |||||||
| chr17:81405104 | G | A | 1 | a0004c0004t0002g0061 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.178+5187G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405104 | |||||||
| chr17:81405380 | A | T | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.178+5463A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405380 | |||||||
| chr17:81405589 | C | T | 2 | a0003c0002t0004g0205 a0038c0083t0003g0129 |
2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.178+5672C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405589 | |||||||
| chr17:81405739 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.178+5822C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405739 | |||||||
| chr17:81405944 | T | C | 1 | a0011c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.178+6027T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405944 | |||||||
| chr17:81405955 | C | G | 2 | a0007c0007t0001g0257 a0007c0007t0004g0317 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+6038C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81405955 | |||||||
| chr17:81406149 | C | G | 1 | a0006c0006t0001g0201 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.178+6232C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406149 | |||||||
| chr17:81406219 | G | A | 1 | a0003c0002t0001g0062 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.178+6302G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406219 | |||||||
| chr17:81406229 | GCTCCTGG others(24): Show |
G | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178+6317_178+6347d others(33): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81406229 | ||||||
| chr17:81406340 | G | A | 3 | a0003c0002t0013g0025 a0013c0027t0001g0024 a0013c0027t0001g0026 |
3 | HG02559.hp2 HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.178+6423G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406340 | |||||||
| chr17:81406375 | G | A | 2 | a0004c0004t0002g0214 a0004c0004t0002g0217 |
2 | HG02486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.178+6458G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406375 | |||||||
| chr17:81406453 | G | A | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.178+6536G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406453 | |||||||
| chr17:81406490 | C | T | 3 | a0002c0010t0016g0161 a0002c0103t0026g0245 a0036c0045t0004g0273 |
3 | HG02615.hp1 HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.178+6573C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406490 | |||||||
| chr17:81406620 | C | G | 1 | a0019c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178+6703C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406620 | |||||||
| chr17:81406633 | G | A | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.178+6716G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406633 | |||||||
| chr17:81406703 | G | C | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+6786G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406703 | |||||||
| chr17:81406747 | T | C | 182 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(179): Show |
185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.178+6830T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406747 | |||||||
| chr17:81406750 | G | A | 1 | a0003c0063t0005g0198 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.178+6833G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406750 | |||||||
| chr17:81406814 | C | T | 92 | a0001c0001t0001g0037 a0001c0001t0001g0244 a0001c0001t0001g0274 others(89): Show |
93 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.178+6897C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81406814 | |||||||
| chr17:81407361 | G | T | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+7444G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81407361 | |||||||
| chr17:81407640 | G | A | 1 | a0002c0003t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.178+7723G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81407640 | |||||||
| chr17:81407867 | A | ACAACTGG others(8): Show |
1 | a0001c0001t0001g0224 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.178+7951_178+7965d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81407867 | ||||||
| chr17:81407935 | G | A | 16 | a0001c0001t0001g0274 a0002c0008t0030g0264 a0002c0010t0033g0135 others(13): Show |
17 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+8018G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81407935 | |||||||
| chr17:81407955 | C | T | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.178+8038C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81407955 | |||||||
| chr17:81408016 | G | A | 1 | a0002c0003t0003g0286 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.178+8099G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408016 | |||||||
| chr17:81408029 | C | T | 1 | a0002c0008t0006g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.178+8112C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408029 | |||||||
| chr17:81408042 | C | T | 3 | a0004c0004t0002g0167 a0004c0004t0002g0240 a0004c0004t0002g0241 |
3 | HG00642.hp1 HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.178+8125C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408042 | |||||||
| chr17:81408074 | C | A | 1 | a0012c0031t0004g0016 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.178+8157C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408074 | |||||||
| chr17:81408117 | G | C | 321 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(318): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.178+8200G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408117 | |||||||
| chr17:81408210 | G | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0136 a0001c0001t0001g0169 others(64): Show |
69 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.178+8293G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408210 | |||||||
| chr17:81408215 | G | A | 3 | a0002c0008t0024g0248 a0002c0010t0015g0275 a0028c0044t0001g0249 |
3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.178+8298G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408215 | |||||||
| chr17:81408298 | G | T | 14 | a0001c0001t0001g0274 a0002c0008t0030g0264 a0002c0021t0002g0262 others(11): Show |
15 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+8381G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408298 | |||||||
| chr17:81408486 | C | T | 18 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0002c0003t0003g0110 others(15): Show |
19 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.178+8569C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408486 | |||||||
| chr17:81408563 | G | A | 3 | a0004c0004t0002g0138 a0004c0004t0002g0156 a0004c0004t0022g0139 |
3 | HG03195.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.178+8646G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408563 | |||||||
| chr17:81408616 | C | T | 87 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0035 others(84): Show |
88 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.178+8699C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408616 | |||||||
| chr17:81408746 | G | A | 1 | a0002c0003t0003g0059 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.178+8829G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408746 | |||||||
| chr17:81408773 | C | A | 1 | a0001c0016t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.178+8856C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408773 | |||||||
| chr17:81408971 | C | T | 3 | a0003c0002t0001g0039 a0003c0002t0001g0095 a0003c0002t0001g0096 |
3 | NA18948.hp1 NA18966.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.178+9054C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81408971 | |||||||
| chr17:81409038 | C | T | 1 | a0002c0003t0010g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.178+9121C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409038 | |||||||
| chr17:81409079 | G | A | 14 | a0001c0001t0001g0274 a0002c0008t0030g0264 a0002c0021t0002g0262 others(11): Show |
15 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+9162G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409079 | |||||||
| chr17:81409159 | A | G | 1 | a0002c0010t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178+9242A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409159 | |||||||
| chr17:81409345 | TG | T | 131 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0035 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.178+9433delG | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81409345 | ||||||
| chr17:81409399 | G | A | 1 | a0013c0096t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.178+9482G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409399 | |||||||
| chr17:81409406 | G | C | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.178+9489G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409406 | |||||||
| chr17:81409427 | A | G | 4 | a0010c0014t0001g0243 a0016c0106t0010g0328 a0018c0105t0001g0250 others(1): Show |
4 | HG00639.hp1 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+9510A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409427 | |||||||
| chr17:81409434 | C | T | 66 | a0001c0001t0001g0244 a0001c0001t0001g0281 a0001c0001t0001g0282 others(63): Show |
67 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.178+9517C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409434 | |||||||
| chr17:81409509 | G | C | 3 | a0016c0106t0010g0328 a0018c0105t0001g0250 a0041c0107t0002g0251 |
3 | HG02486.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.178+9592G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409509 | |||||||
| chr17:81409539 | C | T | 2 | a0001c0001t0001g0113 a0002c0009t0004g0121 |
2 | HG01952.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.178+9622C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409539 | |||||||
| chr17:81409551 | C | T | 6 | a0001c0001t0001g0274 a0001c0001t0001g0320 a0002c0008t0025g0253 others(3): Show |
6 | HG01261.hp2 HG01884.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+9634C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409551 | |||||||
| chr17:81409611 | A | G | 11 | a0001c0001t0006g0149 a0001c0061t0007g0152 a0002c0003t0003g0231 others(8): Show |
11 | HG00639.hp2 HG00738.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+9694A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409611 | |||||||
| chr17:81409650 | C | T | 1 | a0002c0003t0003g0230 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.178+9733C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409650 | |||||||
| chr17:81409793 | C | A | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.178+9876C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409793 | |||||||
| chr17:81409804 | G | T | 2 | a0002c0003t0003g0044 a0003c0002t0004g0295 |
2 | NA18942.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.178+9887G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409804 | |||||||
| chr17:81409814 | G | A | 73 | a0001c0001t0001g0108 a0001c0001t0001g0176 a0001c0001t0001g0225 others(70): Show |
74 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.178+9897G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409814 | |||||||
| chr17:81409814 | G | C | 1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.178+9897G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409814 | |||||||
| chr17:81409896 | G | C | 2 | a0005c0064t0005g0178 a0035c0033t0001g0179 |
2 | HG02523.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.178+9979G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409896 | |||||||
| chr17:81409928 | C | T | 1 | a0028c0044t0001g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.178+10011C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409928 | |||||||
| chr17:81409936 | C | T | 1 | a0009c0024t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.178+10019C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81409936 | |||||||
| chr17:81410178 | C | A | 1 | a0001c0080t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.178+10261C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410178 | |||||||
| chr17:81410193 | G | A | 1 | a0002c0010t0016g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.178+10276G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410193 | |||||||
| chr17:81410221 | C | G | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+10304C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410221 | |||||||
| chr17:81410288 | C | A | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+10371C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410288 | |||||||
| chr17:81410288 | C | G | 20 | a0001c0001t0002g0132 a0001c0001t0006g0149 a0001c0001t0007g0145 others(17): Show |
20 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.178+10371C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410288 | |||||||
| chr17:81410384 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+10467G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410384 | |||||||
| chr17:81410423 | G | A | 1 | a0019c0030t0007g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.178+10506G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410423 | |||||||
| chr17:81410461 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.178+10544T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410461 | |||||||
| chr17:81410531 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+10614G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410531 | |||||||
| chr17:81410535 | C | T | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+10618C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410535 | |||||||
| chr17:81410536 | G | A | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178+10619G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410536 | |||||||
| chr17:81410539 | G | A | 1 | a0019c0030t0007g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.178+10622G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410539 | |||||||
| chr17:81410590 | G | C | 2 | a0001c0001t0001g0225 a0005c0028t0001g0226 |
2 | NA18944.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.178+10673G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410590 | |||||||
| chr17:81410591 | A | T | 2 | a0001c0001t0001g0225 a0005c0028t0001g0226 |
2 | NA18944.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.178+10674A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410591 | |||||||
| chr17:81410591 | AGGCACCA others(8): Show |
A | 3 | a0002c0019t0003g0315 a0005c0005t0005g0202 a0007c0007t0004g0317 |
3 | NA18983.hp1 NA19043.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.178+10701_178+1071 others(19): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81410591 | ||||||
| chr17:81410605 | C | G | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+10688C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410605 | |||||||
| chr17:81410606 | T | A | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+10689T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410606 | |||||||
| chr17:81410614 | C | T | 2 | a0001c0001t0031g0196 a0002c0012t0002g0058 |
2 | HG01358.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.178+10697C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410614 | |||||||
| chr17:81410729 | C | G | 28 | a0001c0062t0020g0252 a0002c0008t0025g0253 a0002c0008t0037g0319 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.178+10812C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410729 | |||||||
| chr17:81410824 | C | G | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+10907C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81410824 | |||||||
| chr17:81411019 | A | G | 91 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(88): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.178+11102A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411019 | |||||||
| chr17:81411236 | G | A | 2 | a0010c0014t0001g0243 a0019c0030t0007g0239 |
2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.178+11319G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411236 | |||||||
| chr17:81411244 | C | T | 81 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0035 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.178+11327C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411244 | |||||||
| chr17:81411310 | C | T | 4 | a0002c0008t0030g0264 a0002c0021t0002g0262 a0040c0046t0027g0263 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+11393C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411310 | |||||||
| chr17:81411346 | A | G | 312 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(309): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.178+11429A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411346 | |||||||
| chr17:81411351 | C | T | 1 | a0002c0008t0025g0253 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.178+11434C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411351 | |||||||
| chr17:81411474 | C | CCCTG | 47 | a0001c0001t0001g0131 a0001c0001t0001g0174 a0001c0001t0001g0225 others(44): Show |
47 | HG00544.hp1 HG00735.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.178+11597_178+1160 others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | ||||||
| chr17:81411474 | C | CCCTGCCT others(1): Show |
49 | a0001c0001t0001g0037 a0001c0001t0001g0169 a0001c0001t0001g0244 others(46): Show |
50 | HG00438.hp1 HG00642.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.178+11593_178+1160 others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | ||||||
| chr17:81411474 | C | CCCTGCCT others(5): Show |
13 | a0001c0001t0001g0176 a0001c0001t0001g0279 a0001c0001t0001g0281 others(10): Show |
13 | HG02027.hp1 HG02071.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+11589_178+1160 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | ||||||
| chr17:81411474 | C | CCCTGCCT others(9): Show |
2 | a0002c0003t0003g0293 a0003c0002t0004g0194 |
2 | HG00408.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.178+11585_178+1160 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | ||||||
| chr17:81411474 | C | CCCTGCCT others(13): Show |
1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+11581_178+1160 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | ||||||
| chr17:81411474 | C | CCCTGCCT others(17): Show |
1 | a0003c0002t0013g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178+11577_178+1160 others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | ||||||
| chr17:81411474 | CCCTG | C | 5 | a0002c0008t0030g0264 a0002c0008t0037g0319 a0002c0021t0002g0262 others(2): Show |
5 | HG02055.hp1 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+11597_178+1160 others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | ||||||
| chr17:81411474 | CCCTGCCT others(1): Show |
C | 9 | a0004c0004t0002g0003 a0004c0004t0002g0266 a0004c0004t0002g0269 others(6): Show |
10 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.178+11593_178+1160 others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | ||||||
| chr17:81411474 | CCCTGCCT others(5): Show |
C | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+11589_178+1160 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411474 | ||||||
| chr17:81411490 | GCCTGCCT others(33): Show |
G | 1 | a0013c0096t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.178+11577_178+1161 others(44): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411490 | ||||||
| chr17:81411490 | GCCTGCCT others(37): Show |
G | 2 | a0002c0010t0009g0260 a0017c0023t0015g0277 |
2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.178+11577_178+1162 others(48): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411490 | ||||||
| chr17:81411494 | G | T | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+11577G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411494 | |||||||
| chr17:81411494 | GCCTGCCT others(29): Show |
G | 1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.178+11581_178+1161 others(40): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411494 | ||||||
| chr17:81411494 | GCCTGCCT others(33): Show |
G | 1 | a0002c0010t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178+11581_178+1162 others(44): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411494 | ||||||
| chr17:81411502 | GCCTGCCT others(9): Show |
G | 1 | a0001c0001t0001g0086 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.178+11589_178+1160 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411502 | ||||||
| chr17:81411502 | GCCTGCCT others(13): Show |
G | 2 | a0002c0010t0016g0234 a0017c0023t0038g0027 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.178+11589_178+1160 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411502 | ||||||
| chr17:81411502 | GCCTGCCT others(21): Show |
G | 1 | a0013c0027t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.178+11589_178+1161 others(32): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411502 | ||||||
| chr17:81411506 | GCCTGCCT others(5): Show |
G | 1 | a0020c0038t0002g0143 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178+11593_178+1160 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411506 | ||||||
| chr17:81411506 | GCCTGCCT others(13): Show |
G | 14 | a0001c0062t0020g0252 a0002c0008t0025g0253 a0002c0012t0002g0137 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+11593_178+1161 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411506 | ||||||
| chr17:81411506 | GCCTGCCT others(17): Show |
G | 1 | a0013c0027t0001g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.178+11593_178+1161 others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411506 | ||||||
| chr17:81411510 | GCCTGCCT others(5): Show |
G | 2 | a0002c0008t0024g0248 a0007c0007t0001g0257 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.178+11597_178+1160 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411510 | ||||||
| chr17:81411510 | GCCTGCCT others(9): Show |
G | 3 | a0002c0003t0003g0233 a0003c0018t0002g0144 a0056c0104t0010g0160 |
3 | HG00642.hp2 HG01175.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.178+11597_178+1161 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411510 | ||||||
| chr17:81411514 | G | GCCTGCCT others(13): Show |
2 | a0002c0092t0001g0146 a0021c0094t0002g0147 |
2 | HG00733.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178+11600_178+1160 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | G | GCCTGCCT others(9): Show |
1 | a0034c0069t0003g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.178+11600_178+1160 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | G | GCCTGCCT others(5): Show |
3 | a0002c0003t0003g0059 a0002c0091t0004g0227 a0005c0095t0005g0199 |
3 | HG01943.hp1 NA18963.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.178+11600_178+1160 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | G | GCCTGCCT others(13): Show |
1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178+11600_178+1160 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | G | GCCTGCCT others(17): Show |
1 | a0035c0033t0001g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.178+11600_178+1160 others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | G | GCCTGCCT others(1): Show |
4 | a0001c0016t0001g0181 a0002c0003t0003g0046 a0006c0006t0001g0201 others(1): Show |
4 | HG00673.hp1 HG01192.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+11600_178+1160 others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | G | GCCTGCCT others(9): Show |
1 | a0002c0003t0003g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.178+11600_178+1160 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | G | GCCTT | 8 | a0001c0001t0001g0279 a0001c0001t0001g0285 a0002c0003t0003g0047 others(5): Show |
8 | HG00544.hp1 HG01516.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+11654_178+1165 others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | G | GCCTTCCT others(1): Show |
3 | a0001c0001t0001g0291 a0001c0001t0002g0177 a0039c0087t0004g0165 |
3 | HG02683.hp2 HG03491.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.178+11650_178+1165 others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | G | GCCTTCCT others(5): Show |
2 | a0003c0002t0004g0280 a0038c0083t0003g0129 |
2 | HG03490.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.178+11646_178+1165 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | G | T | 2 | a0002c0093t0009g0015 a0014c0022t0036g0318 |
2 | HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.178+11597G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411514 | |||||||
| chr17:81411514 | GCCTT | G | 70 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0035 others(67): Show |
70 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.178+11654_178+1165 others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | GCCTTCCT others(1): Show |
G | 29 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0223 others(26): Show |
32 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.178+11650_178+1165 others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | GCCTTCCT others(5): Show |
G | 20 | a0001c0001t0001g0108 a0001c0001t0001g0276 a0001c0001t0001g0326 others(17): Show |
20 | HG00609.hp2 HG00639.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.178+11646_178+1165 others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | GCCTTCCT others(9): Show |
G | 15 | a0001c0001t0001g0321 a0001c0075t0001g0303 a0002c0003t0003g0302 others(12): Show |
15 | HG01243.hp2 HG02055.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.178+11642_178+1165 others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411514 | GCCTTCCT others(13): Show |
G | 3 | a0001c0001t0001g0320 a0006c0020t0002g0325 a0007c0007t0004g0317 |
3 | HG01074.hp2 HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.178+11638_178+1165 others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81411514 | ||||||
| chr17:81411518 | T | G | 70 | a0001c0001t0001g0030 a0001c0001t0001g0131 a0001c0001t0001g0169 others(67): Show |
70 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.178+11601T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411518 | |||||||
| chr17:81411522 | T | G | 46 | a0001c0001t0001g0142 a0001c0001t0001g0174 a0001c0001t0002g0084 others(43): Show |
46 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.178+11605T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411522 | |||||||
| chr17:81411526 | T | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0006g0149 others(19): Show |
24 | HG00544.hp2 HG01168.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.178+11609T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411526 | |||||||
| chr17:81411530 | T | G | 23 | a0001c0001t0001g0109 a0001c0001t0001g0276 a0001c0043t0001g0164 others(20): Show |
24 | HG00609.hp2 HG00639.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.178+11613T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411530 | |||||||
| chr17:81411534 | T | G | 1 | a0028c0044t0001g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.178+11617T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411534 | |||||||
| chr17:81411566 | T | C | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178+11649T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411566 | |||||||
| chr17:81411577 | G | C | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178+11660G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411577 | |||||||
| chr17:81411952 | C | T | 2 | a0001c0001t0001g0276 a0019c0030t0007g0032 |
2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.178+12035C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411952 | |||||||
| chr17:81411966 | G | A | 1 | a0003c0002t0001g0074 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.178+12049G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81411966 | |||||||
| chr17:81412074 | G | A | 1 | a0002c0010t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178+12157G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412074 | |||||||
| chr17:81412151 | C | T | 2 | a0001c0001t0001g0274 a0019c0030t0007g0239 |
2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.178+12234C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412151 | |||||||
| chr17:81412169 | C | T | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178+12252C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412169 | |||||||
| chr17:81412187 | C | T | 1 | a0006c0006t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.178+12270C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412187 | |||||||
| chr17:81412305 | T | C | 28 | a0001c0062t0020g0252 a0002c0008t0025g0253 a0002c0008t0037g0319 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.178+12388T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412305 | |||||||
| chr17:81412491 | T | G | 1 | a0002c0084t0001g0070 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.178+12574T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412491 | |||||||
| chr17:81412494 | G | A | 6 | a0001c0001t0001g0176 a0003c0002t0004g0182 a0003c0002t0004g0194 others(3): Show |
6 | HG02738.hp1 HG03491.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+12577G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412494 | |||||||
| chr17:81412628 | C | T | 1 | a0007c0007t0001g0005 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.178+12711C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412628 | |||||||
| chr17:81412662 | G | A | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178+12745G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412662 | |||||||
| chr17:81412698 | C | T | 1 | a0002c0008t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.178+12781C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412698 | |||||||
| chr17:81412789 | T | C | 1 | a0018c0105t0001g0250 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.178+12872T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412789 | |||||||
| chr17:81412793 | A | T | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.178+12876A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412793 | |||||||
| chr17:81412854 | T | C | 1 | a0044c0081t0001g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.178+12937T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412854 | |||||||
| chr17:81412953 | A | C | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.178+13036A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412953 | |||||||
| chr17:81412956 | G | A | 1 | a0002c0099t0003g0051 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.178+13039G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412956 | |||||||
| chr17:81412962 | C | T | 3 | a0001c0062t0020g0252 a0002c0008t0025g0253 a0002c0068t0007g0254 |
3 | HG01261.hp2 HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.178+13045C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412962 | |||||||
| chr17:81412981 | C | T | 1 | a0003c0002t0035g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.178+13064C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81412981 | |||||||
| chr17:81413059 | C | T | 44 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(41): Show |
45 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.178+13142C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413059 | |||||||
| chr17:81413144 | G | A | 1 | a0037c0089t0002g0265 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.178+13227G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413144 | |||||||
| chr17:81413152 | A | G | 28 | a0001c0062t0020g0252 a0002c0003t0003g0184 a0002c0008t0025g0253 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.178+13235A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413152 | |||||||
| chr17:81413214 | G | C | 4 | a0001c0001t0001g0030 a0001c0001t0002g0177 a0001c0001t0005g0064 others(1): Show |
4 | HG02683.hp2 HG03654.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+13297G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413214 | |||||||
| chr17:81413258 | G | A | 1 | a0011c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.178+13341G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413258 | |||||||
| chr17:81413329 | G | T | 1 | a0002c0008t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.178+13412G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413329 | |||||||
| chr17:81413400 | C | T | 1 | a0044c0081t0001g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.179-13400C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413400 | |||||||
| chr17:81413413 | G | C | 2 | a0001c0001t0001g0274 a0019c0030t0007g0239 |
2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.179-13387G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413413 | |||||||
| chr17:81413493 | C | T | 1 | a0004c0004t0002g0127 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.179-13307C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413493 | |||||||
| chr17:81413571 | G | A | 5 | a0002c0010t0009g0260 a0013c0096t0001g0235 a0017c0023t0015g0277 others(2): Show |
5 | HG00099.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-13229G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413571 | |||||||
| chr17:81413603 | C | A | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-13197C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413603 | |||||||
| chr17:81413651 | C | T | 50 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0225 others(47): Show |
51 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.179-13149C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413651 | |||||||
| chr17:81413683 | G | A | 1 | a0001c0061t0007g0152 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.179-13117G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413683 | |||||||
| chr17:81413692 | C | G | 316 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(313): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.179-13108C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413692 | |||||||
| chr17:81413695 | G | T | 4 | a0001c0001t0031g0196 a0002c0012t0002g0058 a0002c0012t0002g0159 others(1): Show |
4 | HG01346.hp2 HG01358.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-13105G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413695 | |||||||
| chr17:81413736 | C | G | 216 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(213): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.179-13064C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413736 | |||||||
| chr17:81413744 | G | A | 4 | a0002c0003t0003g0067 a0004c0004t0002g0167 a0004c0004t0002g0240 others(1): Show |
4 | HG00642.hp1 HG01167.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-13056G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413744 | |||||||
| chr17:81413750 | G | A | 29 | a0001c0062t0020g0252 a0002c0003t0003g0184 a0002c0008t0025g0253 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.179-13050G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413750 | |||||||
| chr17:81413842 | G | A | 6 | a0001c0001t0001g0274 a0002c0010t0009g0260 a0007c0007t0004g0317 others(3): Show |
6 | HG02615.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-12958G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413842 | |||||||
| chr17:81413853 | C | T | 2 | a0002c0010t0016g0234 a0017c0023t0038g0027 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.179-12947C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413853 | |||||||
| chr17:81413933 | C | T | 1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.179-12867C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413933 | |||||||
| chr17:81413934 | G | A | 1 | a0002c0008t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-12866G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413934 | |||||||
| chr17:81413977 | C | G | 1 | a0002c0008t0004g0117 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.179-12823C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81413977 | |||||||
| chr17:81414069 | C | T | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-12731C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414069 | |||||||
| chr17:81414084 | G | T | 2 | a0002c0010t0009g0260 a0017c0023t0015g0277 |
2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-12716G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414084 | |||||||
| chr17:81414232 | G | A | 12 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0002c0009t0009g0185 others(9): Show |
12 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-12568G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414232 | |||||||
| chr17:81414582 | C | T | 1 | a0028c0044t0001g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.179-12218C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414582 | |||||||
| chr17:81414678 | G | C | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-12122G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414678 | |||||||
| chr17:81414717 | G | A | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-12083G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414717 | |||||||
| chr17:81414722 | G | A | 3 | a0001c0001t0001g0276 a0002c0010t0015g0275 a0019c0030t0007g0032 |
3 | HG02723.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.179-12078G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414722 | |||||||
| chr17:81414890 | C | T | 1 | a0002c0008t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-11910C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414890 | |||||||
| chr17:81414949 | C | T | 44 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(41): Show |
45 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.179-11851C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414949 | |||||||
| chr17:81414992 | G | T | 1 | a0019c0030t0007g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.179-11808G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81414992 | |||||||
| chr17:81415004 | C | T | 3 | a0001c0001t0001g0274 a0002c0025t0003g0212 a0019c0030t0007g0239 |
3 | HG02015.hp2 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.179-11796C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415004 | |||||||
| chr17:81415015 | G | A | 1 | a0046c0052t0001g0195 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.179-11785G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415015 | |||||||
| chr17:81415070 | CG | C | 32 | a0001c0062t0020g0252 a0002c0008t0025g0253 a0002c0008t0037g0319 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.179-11728delG | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81415070 | ||||||
| chr17:81415123 | G | A | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-11677G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415123 | |||||||
| chr17:81415310 | C | G | 1 | a0004c0011t0004g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.179-11490C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415310 | |||||||
| chr17:81415359 | G | A | 1 | a0002c0003t0003g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.179-11441G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415359 | |||||||
| chr17:81415371 | G | A | 4 | a0002c0009t0009g0185 a0012c0031t0004g0018 a0012c0102t0004g0017 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-11429G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415371 | |||||||
| chr17:81415446 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.179-11354G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415446 | |||||||
| chr17:81415451 | C | T | 298 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(295): Show |
301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.179-11349C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415451 | |||||||
| chr17:81415611 | C | T | 12 | a0002c0012t0002g0137 a0003c0018t0002g0144 a0004c0004t0002g0092 others(9): Show |
12 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-11189C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415611 | |||||||
| chr17:81415667 | G | T | 2 | a0002c0010t0009g0260 a0017c0023t0015g0277 |
2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-11133G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415667 | |||||||
| chr17:81415686 | G | A | 224 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(221): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.179-11114G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415686 | |||||||
| chr17:81415692 | G | A | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-11108G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415692 | |||||||
| chr17:81415749 | G | A | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-11051G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415749 | |||||||
| chr17:81415861 | C | T | 2 | a0002c0019t0003g0315 a0005c0005t0005g0202 |
2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-10939C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415861 | |||||||
| chr17:81415879 | C | T | 12 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0001t0001g0276 others(9): Show |
12 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-10921C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415879 | |||||||
| chr17:81415935 | C | G | 1 | a0004c0004t0002g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.179-10865C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415935 | |||||||
| chr17:81415944 | A | G | 5 | a0001c0001t0001g0276 a0002c0010t0015g0275 a0002c0068t0007g0254 others(2): Show |
5 | HG00639.hp1 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-10856A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81415944 | |||||||
| chr17:81416007 | CGT | C | 5 | a0002c0010t0009g0260 a0004c0011t0002g0163 a0008c0013t0006g0162 others(2): Show |
5 | HG01074.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-10782_179-1078 others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416007 | ||||||
| chr17:81416009 | T | C | 2 | a0002c0019t0003g0315 a0005c0005t0005g0202 |
2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-10791T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416009 | |||||||
| chr17:81416011 | T | C | 2 | a0005c0005t0008g0296 a0005c0005t0008g0297 |
2 | HG01069.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.179-10789T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416011 | |||||||
| chr17:81416011 | TGTGTGTG others(31): Show |
T | 3 | a0001c0001t0001g0274 a0019c0030t0007g0032 a0019c0030t0007g0239 |
3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-10761_179-1072 others(42): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416011 | ||||||
| chr17:81416051 | T | C | 3 | a0001c0001t0001g0274 a0019c0030t0007g0032 a0019c0030t0007g0239 |
3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-10749T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416051 | |||||||
| chr17:81416065 | G | A | 42 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(39): Show |
43 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.179-10735G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416065 | |||||||
| chr17:81416074 | A | G | 1 | a0003c0002t0004g0205 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.179-10726A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416074 | |||||||
| chr17:81416087 | C | T | 1 | a0002c0012t0002g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.179-10713C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416087 | |||||||
| chr17:81416107 | GGTGT | G | 42 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(39): Show |
43 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.179-10684_179-1068 others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416107 | ||||||
| chr17:81416248 | G | A | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-10552G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416248 | |||||||
| chr17:81416253 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.179-10547C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416253 | |||||||
| chr17:81416317 | C | T | 2 | a0013c0027t0001g0024 a0013c0027t0001g0026 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.179-10483C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416317 | |||||||
| chr17:81416397 | C | T | 5 | a0001c0001t0001g0327 a0002c0009t0009g0185 a0012c0031t0004g0018 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-10403C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416397 | |||||||
| chr17:81416439 | CGT | C | 9 | a0001c0001t0006g0149 a0001c0001t0007g0145 a0001c0061t0007g0152 others(6): Show |
9 | HG00738.hp1 HG02300.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-10350_179-1034 others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416439 | ||||||
| chr17:81416460 | G | GGT | 5 | a0002c0010t0016g0234 a0002c0093t0009g0015 a0004c0011t0002g0023 others(2): Show |
5 | HG02109.hp1 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-10321_179-1032 others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416460 | ||||||
| chr17:81416477 | G | GTATGTGT others(63): Show |
1 | a0001c0001t0002g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.179-10322_179-1032 others(74): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTCCATGA others(57): Show |
4 | a0016c0106t0010g0328 a0018c0105t0001g0250 a0028c0044t0001g0249 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-10322_179-1032 others(68): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTCC others(71): Show |
1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-10320_179-1031 others(82): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTCC others(69): Show |
6 | a0001c0001t0001g0324 a0001c0001t0001g0326 a0002c0101t0010g0020 others(3): Show |
6 | HG01074.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(80): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTCC others(61): Show |
6 | a0001c0001t0007g0145 a0001c0016t0001g0052 a0001c0061t0007g0152 others(3): Show |
6 | HG00738.hp1 HG01978.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(72): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTCC others(71): Show |
72 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0276 others(69): Show |
74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(82): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTGT others(63): Show |
1 | a0056c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.179-10320_179-1031 others(74): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTGT others(61): Show |
1 | a0042c0058t0002g0008 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.179-10320_179-1031 others(72): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTGT others(63): Show |
195 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0033 others(192): Show |
195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(74): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTGT others(73): Show |
4 | a0002c0010t0009g0260 a0003c0002t0013g0025 a0013c0096t0001g0235 others(1): Show |
4 | HG02615.hp2 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(84): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTGT others(63): Show |
2 | a0002c0003t0003g0230 a0051c0100t0001g0237 |
2 | NA18969.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.179-10320_179-1031 others(74): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTGT others(65): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0089 a0001c0001t0007g0090 others(8): Show |
13 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-10320_179-1031 others(76): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416477 | G | GTGTGTGT others(77): Show |
1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-10320_179-1031 others(88): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416477 | ||||||
| chr17:81416498 | T | TGC | 304 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(301): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.179-10301_179-1030 others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416498 | ||||||
| chr17:81416498 | T | TGCGTGTG others(69): Show |
1 | a0001c0001t0001g0327 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.179-10300_179-1029 others(80): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416498 | ||||||
| chr17:81416498 | T | TGCGTGTG others(69): Show |
2 | a0002c0019t0003g0315 a0005c0005t0005g0202 |
2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-10300_179-1029 others(80): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416498 | ||||||
| chr17:81416498 | T | TGCGTGTG others(61): Show |
4 | a0001c0001t0001g0037 a0001c0001t0001g0136 a0002c0099t0003g0051 others(1): Show |
4 | HG00438.hp1 HG02074.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-10300_179-1029 others(72): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416498 | ||||||
| chr17:81416498 | T | TGCGTGTG others(71): Show |
6 | a0002c0008t0024g0248 a0002c0026t0003g0247 a0007c0007t0001g0257 others(3): Show |
6 | HG02559.hp2 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-10300_179-1029 others(82): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416498 | ||||||
| chr17:81416570 | CGT | C | 225 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(222): Show |
227 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.179-10219_179-1021 others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81416570 | ||||||
| chr17:81416601 | C | T | 1 | a0002c0101t0010g0020 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.179-10199C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416601 | |||||||
| chr17:81416604 | G | A | 1 | a0001c0051t0001g0045 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.179-10196G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416604 | |||||||
| chr17:81416605 | T | C | 1 | a0013c0096t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-10195T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416605 | |||||||
| chr17:81416612 | G | A | 1 | a0019c0030t0007g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.179-10188G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416612 | |||||||
| chr17:81416624 | A | C | 1 | a0013c0096t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-10176A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416624 | |||||||
| chr17:81416708 | C | T | 31 | a0001c0062t0020g0252 a0002c0008t0025g0253 a0002c0008t0037g0319 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.179-10092C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416708 | |||||||
| chr17:81416726 | C | T | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-10074C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416726 | |||||||
| chr17:81416926 | C | T | 1 | a0002c0003t0003g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.179-9874C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81416926 | |||||||
| chr17:81417122 | G | C | 4 | a0002c0009t0009g0185 a0012c0031t0004g0018 a0012c0102t0004g0017 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-9678G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417122 | |||||||
| chr17:81417153 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0203 others(2): Show |
5 | HG00408.hp2 HG02886.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-9647G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417153 | |||||||
| chr17:81417164 | C | T | 1 | a0002c0003t0003g0300 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.179-9636C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417164 | |||||||
| chr17:81417179 | G | A | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-9621G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417179 | |||||||
| chr17:81417195 | C | T | 1 | a0002c0003t0003g0046 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.179-9605C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417195 | |||||||
| chr17:81417268 | G | A | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-9532G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417268 | |||||||
| chr17:81417274 | C | T | 3 | a0002c0010t0009g0260 a0013c0096t0001g0235 a0017c0023t0015g0277 |
3 | HG02615.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-9526C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417274 | |||||||
| chr17:81417300 | T | TGGTTGCA others(7): Show |
1 | a0003c0002t0004g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.179-9498_179-9485d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417300 | ||||||
| chr17:81417398 | G | A | 1 | a0003c0002t0001g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.179-9402G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417398 | |||||||
| chr17:81417423 | A | G | 2 | a0007c0007t0004g0317 a0036c0045t0004g0273 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.179-9377A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417423 | |||||||
| chr17:81417514 | G | A | 2 | a0002c0019t0003g0315 a0005c0005t0005g0202 |
2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-9286G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417514 | |||||||
| chr17:81417555 | A | AC | 32 | a0001c0001t0001g0157 a0001c0001t0001g0276 a0001c0062t0020g0252 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.179-9235dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417555 | ||||||
| chr17:81417555 | A | ACC | 36 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(33): Show |
37 | HG00609.hp2 HG01168.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.179-9236_179-9235d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417555 | ||||||
| chr17:81417555 | A | ACCG | 93 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.179-9243_179-9242i others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417555 | ||||||
| chr17:81417555 | A | ACCGC | 25 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0136 others(22): Show |
25 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.179-9243_179-9242i others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417555 | ||||||
| chr17:81417560 | C | CCCG | 103 | a0001c0001t0001g0131 a0001c0001t0001g0169 a0001c0001t0001g0174 others(100): Show |
104 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.179-9238_179-9237i others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81417560 | ||||||
| chr17:81417686 | G | C | 318 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(315): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.179-9114G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417686 | |||||||
| chr17:81417945 | C | T | 2 | a0007c0007t0004g0317 a0036c0045t0004g0273 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.179-8855C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81417945 | |||||||
| chr17:81418125 | C | T | 2 | a0002c0019t0003g0315 a0005c0005t0005g0202 |
2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-8675C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418125 | |||||||
| chr17:81418170 | C | T | 2 | a0001c0001t0001g0276 a0002c0068t0007g0254 |
2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.179-8630C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418170 | |||||||
| chr17:81418199 | C | T | 1 | a0002c0003t0003g0067 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.179-8601C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418199 | |||||||
| chr17:81418265 | G | A | 3 | a0002c0008t0024g0248 a0002c0010t0009g0014 a0002c0010t0016g0161 |
3 | HG02630.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.179-8535G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418265 | |||||||
| chr17:81418289 | T | C | 27 | a0001c0062t0020g0252 a0002c0008t0025g0253 a0002c0008t0037g0319 others(24): Show |
28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-8511T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418289 | |||||||
| chr17:81418533 | C | T | 1 | a0002c0008t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-8267C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418533 | |||||||
| chr17:81418538 | C | T | 11 | a0002c0012t0002g0137 a0004c0004t0002g0092 a0004c0004t0002g0093 others(8): Show |
11 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.179-8262C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418538 | |||||||
| chr17:81418568 | C | T | 3 | a0002c0010t0009g0260 a0013c0096t0001g0235 a0017c0023t0015g0277 |
3 | HG02615.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-8232C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418568 | |||||||
| chr17:81418617 | G | C | 4 | a0016c0106t0010g0328 a0018c0105t0001g0250 a0028c0044t0001g0249 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-8183G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418617 | |||||||
| chr17:81418632 | A | G | 2 | a0007c0007t0004g0317 a0036c0045t0004g0273 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.179-8168A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418632 | |||||||
| chr17:81418688 | C | T | 1 | a0011c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.179-8112C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418688 | |||||||
| chr17:81418697 | C | T | 1 | a0003c0002t0004g0194 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.179-8103C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418697 | |||||||
| chr17:81418766 | C | CGT | 33 | a0001c0001t0001g0037 a0001c0001t0001g0274 a0001c0062t0020g0252 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.179-8027_179-8026d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418766 | ||||||
| chr17:81418774 | T | C | 1 | a0027c0079t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.179-8026T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418774 | |||||||
| chr17:81418775 | A | G | 1 | a0027c0079t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.179-8025A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418775 | |||||||
| chr17:81418776 | C | CGTGTGTG others(3): Show |
1 | a0008c0013t0006g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.179-8017_179-8016i others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418776 | ||||||
| chr17:81418776 | C | T | 1 | a0027c0079t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.179-8024C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418776 | |||||||
| chr17:81418776 | CGT | C | 3 | a0002c0010t0033g0135 a0002c0025t0003g0212 a0004c0037t0014g0256 |
3 | HG02015.hp2 HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.179-8015_179-8014d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418776 | ||||||
| chr17:81418777 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.179-8023G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418777 | |||||||
| chr17:81418782 | T | TGC | 29 | a0001c0001t0001g0037 a0001c0062t0020g0252 a0002c0008t0025g0253 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.179-8017_179-8016i others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418782 | ||||||
| chr17:81418784 | T | C | 3 | a0001c0001t0001g0274 a0019c0030t0007g0032 a0019c0030t0007g0239 |
3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-8016T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418784 | |||||||
| chr17:81418787 | A | G | 35 | a0001c0001t0001g0037 a0001c0001t0001g0274 a0001c0062t0020g0252 others(32): Show |
36 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.179-8013A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418787 | |||||||
| chr17:81418788 | C | T | 32 | a0001c0001t0001g0037 a0001c0001t0001g0274 a0001c0062t0020g0252 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.179-8012C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418788 | |||||||
| chr17:81418794 | T | C | 3 | a0001c0001t0001g0274 a0019c0030t0007g0032 a0019c0030t0007g0239 |
3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-8006T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418794 | |||||||
| chr17:81418795 | G | GTGTGCGC others(3): Show |
1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-8005_179-8004i others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418795 | |||||||
| chr17:81418795 | GCGTGTGT others(7): Show |
G | 3 | a0002c0010t0009g0014 a0002c0010t0016g0161 a0010c0014t0001g0243 |
3 | HG00639.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.179-7991_179-7978d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418795 | ||||||
| chr17:81418796 | C | CGCGCAT | 27 | a0001c0001t0001g0037 a0001c0062t0020g0252 a0002c0008t0025g0253 others(24): Show |
28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-8003_179-8002i others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | ||||||
| chr17:81418796 | C | CGCGCATG others(17): Show |
1 | a0001c0073t0001g0055 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.179-8003_179-8002i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | ||||||
| chr17:81418796 | C | CGTGCAT | 3 | a0001c0001t0001g0274 a0019c0030t0007g0032 a0019c0030t0007g0239 |
3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-8001_179-8000i others(8): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | ||||||
| chr17:81418796 | C | CGTGTGCG others(5): Show |
1 | a0002c0021t0002g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.179-7999_179-7998i others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | ||||||
| chr17:81418796 | C | CGTGTGTG others(11): Show |
4 | a0002c0009t0009g0185 a0012c0031t0004g0018 a0012c0102t0004g0017 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-7993_179-7992i others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | ||||||
| chr17:81418796 | C | CGTGTGTG others(13): Show |
16 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0002c0008t0004g0117 others(13): Show |
16 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.179-7992_179-7991i others(22): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418796 | ||||||
| chr17:81418796 | C | T | 3 | a0002c0103t0026g0245 a0008c0013t0006g0162 a0027c0079t0004g0128 |
3 | HG01516.hp1 HG02615.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.179-8004C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418796 | |||||||
| chr17:81418797 | G | GTGTGTGT others(9): Show |
1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-7993_179-7992i others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418797 | ||||||
| chr17:81418797 | G | GTGTGTGT others(11): Show |
6 | a0002c0008t0024g0248 a0003c0002t0004g0310 a0007c0007t0001g0309 others(3): Show |
6 | HG01243.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-7992_179-7991i others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418797 | ||||||
| chr17:81418799 | G | A | 1 | a0004c0011t0002g0120 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.179-8001G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418799 | |||||||
| chr17:81418804 | T | TGTGCGCG others(17): Show |
2 | a0002c0021t0002g0088 a0002c0021t0002g0114 |
2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.179-7993_179-7992i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418804 | ||||||
| chr17:81418804 | T | TGTGTGTG others(19): Show |
1 | a0002c0010t0033g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.179-7992_179-7991i others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418804 | ||||||
| chr17:81418804 | T | TGTGTGTG others(21): Show |
1 | a0035c0033t0001g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.179-7992_179-7991i others(30): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418804 | ||||||
| chr17:81418806 | T | TGTGTGCG others(17): Show |
3 | a0002c0092t0001g0146 a0021c0094t0002g0147 a0022c0034t0002g0216 |
3 | HG00733.hp1 HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.179-7992_179-7991i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418806 | ||||||
| chr17:81418808 | T | C | 3 | a0002c0010t0009g0260 a0013c0096t0001g0235 a0017c0023t0015g0277 |
3 | HG02615.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-7992T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418808 | |||||||
| chr17:81418809 | A | G | 252 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(249): Show |
255 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.179-7991A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418809 | |||||||
| chr17:81418810 | C | CGCATGTG others(17): Show |
1 | a0015c0015t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.179-7989_179-7988i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(5): Show |
1 | a0001c0001t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.179-7989_179-7988i others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(11): Show |
2 | a0002c0019t0003g0315 a0005c0005t0005g0202 |
2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-7989_179-7988i others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(13): Show |
1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-7989_179-7988i others(22): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(15): Show |
7 | a0001c0001t0001g0321 a0001c0075t0001g0303 a0002c0003t0003g0110 others(4): Show |
7 | HG02083.hp1 HG02132.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(17): Show |
28 | a0001c0001t0001g0109 a0001c0043t0001g0164 a0002c0003t0003g0050 others(25): Show |
29 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(19): Show |
1 | a0001c0001t0001g0244 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.179-7989_179-7988i others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(15): Show |
12 | a0001c0001t0031g0196 a0001c0071t0001g0077 a0002c0003t0003g0314 others(9): Show |
12 | HG01167.hp2 HG01169.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(17): Show |
23 | a0001c0001t0001g0242 a0001c0001t0001g0281 a0001c0001t0001g0282 others(20): Show |
23 | HG00738.hp1 HG01070.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(19): Show |
146 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(143): Show |
148 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(28): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(21): Show |
10 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0002c0012t0002g0058 others(7): Show |
10 | HG01346.hp2 HG01952.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(30): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCATG others(23): Show |
1 | a0003c0018t0002g0210 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.179-7989_179-7988i others(32): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCGTG others(13): Show |
1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.179-7989_179-7988i others(22): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCGTG others(11): Show |
1 | a0002c0101t0010g0020 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.179-7989_179-7988i others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGCGCGTG others(15): Show |
5 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0006c0020t0002g0325 others(2): Show |
5 | HG01074.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-7989_179-7988i others(24): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGT | 3 | a0002c0103t0026g0245 a0017c0023t0038g0027 a0036c0045t0004g0273 |
3 | HG02615.hp1 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.179-7969_179-7968d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGTGT | 4 | a0002c0009t0009g0185 a0012c0031t0004g0018 a0012c0102t0004g0017 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-7971_179-7968d others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGTGTGTG others(3): Show |
11 | a0002c0008t0025g0253 a0003c0002t0013g0025 a0003c0018t0002g0144 others(8): Show |
12 | HG00140.hp2 HG00642.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-7977_179-7968d others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGTGTGTG others(5): Show |
6 | a0002c0008t0037g0319 a0002c0012t0002g0137 a0004c0004t0002g0218 others(3): Show |
6 | HG00099.hp1 HG01074.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-7979_179-7968d others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | CGTGTGTG others(7): Show |
6 | a0004c0004t0002g0092 a0004c0004t0002g0093 a0004c0004t0014g0190 others(3): Show |
6 | HG00323.hp2 HG00733.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-7981_179-7968d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418810 | C | T | 9 | a0002c0010t0033g0135 a0002c0021t0002g0088 a0002c0021t0002g0114 others(6): Show |
9 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-7990C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418810 | |||||||
| chr17:81418810 | CGT | C | 3 | a0001c0001t0001g0274 a0002c0021t0002g0262 a0002c0093t0009g0015 |
3 | HG02886.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.179-7969_179-7968d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418810 | ||||||
| chr17:81418811 | G | GCATGTGT others(9): Show |
3 | a0002c0010t0009g0260 a0013c0096t0001g0235 a0017c0023t0015g0277 |
3 | HG02615.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-7989_179-7988i others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418811 | |||||||
| chr17:81418812 | T | C | 3 | a0002c0010t0009g0260 a0013c0096t0001g0235 a0017c0023t0015g0277 |
3 | HG02615.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.179-7988T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418812 | |||||||
| chr17:81418834 | G | T | 4 | a0003c0002t0001g0039 a0003c0002t0001g0095 a0003c0002t0001g0096 others(1): Show |
4 | NA18948.hp1 NA18966.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-7966G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418834 | |||||||
| chr17:81418882 | A | G | 3 | a0001c0001t0001g0274 a0019c0030t0007g0032 a0019c0030t0007g0239 |
3 | HG02886.hp1 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-7918A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81418882 | |||||||
| chr17:81418958 | C | CTGTGCAA others(9): Show |
1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-7811_179-7796d others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81418958 | ||||||
| chr17:81419399 | G | GAATGTGG others(54): Show |
1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-7400_179-7340d others(63): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81419399 | ||||||
| chr17:81419421 | G | T | 43 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(40): Show |
44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.179-7379G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419421 | |||||||
| chr17:81419516 | C | T | 1 | a0019c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-7284C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419516 | |||||||
| chr17:81419566 | C | T | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-7234C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419566 | |||||||
| chr17:81419567 | G | A | 1 | a0056c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.179-7233G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419567 | |||||||
| chr17:81419788 | C | CT | 73 | a0001c0001t0001g0108 a0001c0001t0001g0136 a0001c0001t0001g0187 others(70): Show |
74 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.179-7012_179-7011i others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419788 | |||||||
| chr17:81419788 | C | CTT | 3 | a0002c0003t0003g0067 a0025c0066t0001g0305 a0038c0083t0003g0129 |
3 | HG01433.hp2 HG01943.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.179-7012_179-7011i others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419788 | |||||||
| chr17:81419788 | CG | C | 7 | a0001c0001t0001g0035 a0002c0008t0004g0117 a0007c0047t0002g0308 others(4): Show |
7 | HG01255.hp2 HG01516.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-7011delG | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419788 | |||||||
| chr17:81419789 | G | T | 315 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(312): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.179-7011G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419789 | |||||||
| chr17:81419835 | A | G | 8 | a0004c0004t0002g0003 a0004c0004t0002g0266 a0004c0004t0002g0269 others(5): Show |
9 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-6965A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419835 | |||||||
| chr17:81419882 | C | T | 2 | a0004c0004t0002g0221 a0004c0004t0002g0222 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.179-6918C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419882 | |||||||
| chr17:81419924 | C | T | 4 | a0016c0106t0010g0328 a0018c0105t0001g0250 a0028c0044t0001g0249 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-6876C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419924 | |||||||
| chr17:81419963 | A | G | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-6837A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81419963 | |||||||
| chr17:81420069 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.179-6731C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420069 | |||||||
| chr17:81420221 | C | T | 27 | a0001c0062t0020g0252 a0002c0008t0025g0253 a0002c0008t0037g0319 others(24): Show |
28 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-6579C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420221 | |||||||
| chr17:81420319 | A | C | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-6481A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420319 | |||||||
| chr17:81420410 | C | A | 1 | a0002c0012t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.179-6390C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420410 | |||||||
| chr17:81420412 | C | T | 1 | a0043c0053t0001g0126 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.179-6388C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420412 | |||||||
| chr17:81420488 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.179-6312T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420488 | |||||||
| chr17:81420496 | C | T | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-6304C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420496 | |||||||
| chr17:81420673 | A | G | 1 | a0002c0008t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-6127A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420673 | |||||||
| chr17:81420710 | G | T | 2 | a0002c0008t0024g0248 a0036c0045t0004g0273 |
2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.179-6090G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420710 | |||||||
| chr17:81420736 | A | G | 281 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(278): Show |
284 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.179-6064A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420736 | |||||||
| chr17:81420760 | C | T | 4 | a0002c0009t0009g0185 a0012c0031t0004g0018 a0012c0102t0004g0017 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-6040C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420760 | |||||||
| chr17:81420778 | C | T | 2 | a0001c0001t0001g0320 a0014c0022t0036g0318 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.179-6022C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420778 | |||||||
| chr17:81420813 | C | G | 6 | a0001c0043t0001g0164 a0002c0085t0003g0031 a0003c0002t0001g0124 others(3): Show |
6 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-5987C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420813 | |||||||
| chr17:81420828 | C | G | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-5972C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420828 | |||||||
| chr17:81420892 | A | C | 1 | a0003c0002t0004g0280 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.179-5908A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81420892 | |||||||
| chr17:81421018 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0002g0177 a0001c0001t0005g0064 others(1): Show |
4 | HG02683.hp2 HG03654.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-5782C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421018 | |||||||
| chr17:81421252 | A | G | 321 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(318): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.179-5548A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421252 | |||||||
| chr17:81421438 | C | A | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-5362C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421438 | |||||||
| chr17:81421531 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.179-5269G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421531 | |||||||
| chr17:81421554 | C | T | 1 | a0049c0042t0004g0060 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.179-5246C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421554 | |||||||
| chr17:81421695 | C | T | 1 | a0002c0068t0007g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-5105C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421695 | |||||||
| chr17:81421762 | C | T | 219 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(216): Show |
221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.179-5038C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421762 | |||||||
| chr17:81421763 | G | A | 3 | a0002c0093t0009g0015 a0012c0031t0004g0016 a0037c0089t0002g0265 |
3 | HG02895.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.179-5037G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421763 | |||||||
| chr17:81421821 | C | T | 43 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(40): Show |
44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.179-4979C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421821 | |||||||
| chr17:81421889 | G | A | 43 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(40): Show |
44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.179-4911G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421889 | |||||||
| chr17:81421908 | T | C | 2 | a0019c0030t0007g0032 a0019c0030t0007g0239 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-4892T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421908 | |||||||
| chr17:81421967 | C | T | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-4833C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421967 | |||||||
| chr17:81421983 | G | A | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-4817G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81421983 | |||||||
| chr17:81422014 | A | AT | 219 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(216): Show |
221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.179-4775dupT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81422014 | ||||||
| chr17:81422014 | AT | A | 24 | a0001c0062t0020g0252 a0002c0008t0025g0253 a0002c0008t0037g0319 others(21): Show |
25 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.179-4775delT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81422014 | ||||||
| chr17:81422029 | G | T | 1 | a0017c0023t0015g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.179-4771G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422029 | |||||||
| chr17:81422035 | G | A | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-4765G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422035 | |||||||
| chr17:81422041 | G | A | 1 | a0002c0010t0016g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.179-4759G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422041 | |||||||
| chr17:81422124 | G | A | 1 | a0002c0003t0003g0184 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.179-4676G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422124 | |||||||
| chr17:81422159 | G | A | 3 | a0002c0019t0003g0315 a0005c0005t0005g0202 a0005c0095t0005g0199 |
3 | NA18963.hp2 NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-4641G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422159 | |||||||
| chr17:81422509 | C | T | 1 | a0013c0096t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-4291C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422509 | |||||||
| chr17:81422631 | C | T | 2 | a0007c0007t0001g0257 a0017c0023t0038g0027 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.179-4169C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422631 | |||||||
| chr17:81422649 | C | G | 1 | a0006c0006t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.179-4151C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81422649 | |||||||
| chr17:81423001 | C | T | 1 | a0002c0025t0003g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.179-3799C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423001 | |||||||
| chr17:81423082 | C | A | 2 | a0001c0001t0001g0157 a0004c0004t0002g0158 |
2 | HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.179-3718C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423082 | |||||||
| chr17:81423087 | C | A | 1 | a0003c0002t0001g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.179-3713C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423087 | |||||||
| chr17:81423214 | T | G | 3 | a0002c0019t0003g0315 a0005c0005t0005g0202 a0005c0095t0005g0199 |
3 | NA18963.hp2 NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-3586T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423214 | |||||||
| chr17:81423230 | G | A | 1 | a0002c0010t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.179-3570G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423230 | |||||||
| chr17:81423263 | C | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0292 a0001c0001t0002g0177 others(4): Show |
7 | HG00609.hp1 HG02683.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-3537C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423263 | |||||||
| chr17:81423366 | A | G | 2 | a0019c0030t0007g0032 a0019c0030t0007g0239 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-3434A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423366 | |||||||
| chr17:81423568 | CCCCAGGT others(12): Show |
C | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-3225_179-3207d others(21): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81423568 | ||||||
| chr17:81423621 | C | T | 1 | a0005c0065t0034g0313 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.179-3179C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423621 | |||||||
| chr17:81423650 | T | TG | 5 | a0002c0008t0006g0134 a0003c0002t0001g0096 a0004c0004t0002g0266 others(2): Show |
5 | HG01255.hp1 HG01261.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-3145dupG | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81423650 | ||||||
| chr17:81423658 | G | A | 2 | a0002c0003t0003g0080 a0002c0009t0001g0079 |
2 | HG02015.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.179-3142G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423658 | |||||||
| chr17:81423668 | A | G | 1 | a0002c0003t0010g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.179-3132A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423668 | |||||||
| chr17:81423747 | G | A | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-3053G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423747 | |||||||
| chr17:81423755 | T | C | 3 | a0002c0019t0003g0315 a0005c0005t0005g0202 a0005c0095t0005g0199 |
3 | NA18963.hp2 NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-3045T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423755 | |||||||
| chr17:81423811 | T | G | 97 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0276 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.179-2989T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423811 | |||||||
| chr17:81423878 | C | T | 32 | a0001c0001t0002g0132 a0001c0062t0020g0252 a0002c0008t0025g0253 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.179-2922C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423878 | |||||||
| chr17:81423882 | G | A | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-2918G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423882 | |||||||
| chr17:81423950 | G | A | 1 | a0019c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-2850G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423950 | |||||||
| chr17:81423971 | C | T | 31 | a0001c0001t0002g0132 a0001c0062t0020g0252 a0002c0008t0025g0253 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.179-2829C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423971 | |||||||
| chr17:81423973 | C | T | 3 | a0002c0019t0003g0315 a0005c0005t0005g0202 a0005c0095t0005g0199 |
3 | NA18963.hp2 NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-2827C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81423973 | |||||||
| chr17:81424003 | A | G | 102 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0276 others(99): Show |
104 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.179-2797A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424003 | |||||||
| chr17:81424031 | G | A | 8 | a0002c0009t0004g0301 a0002c0067t0008g0069 a0003c0002t0001g0002 others(5): Show |
9 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-2769G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424031 | |||||||
| chr17:81424160 | G | A | 4 | a0002c0010t0009g0260 a0002c0010t0016g0234 a0013c0096t0001g0235 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-2640G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424160 | |||||||
| chr17:81424260 | C | T | 1 | a0016c0039t0011g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.179-2540C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424260 | |||||||
| chr17:81424489 | T | G | 45 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(42): Show |
46 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.179-2311T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424489 | |||||||
| chr17:81424646 | G | A | 18 | a0001c0001t0001g0279 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
19 | HG00408.hp1 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.179-2154G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424646 | |||||||
| chr17:81424784 | G | A | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0054t0005g0283 |
3 | HG02027.hp1 HG02071.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.179-2016G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424784 | |||||||
| chr17:81424884 | TGTG | T | 3 | a0002c0019t0003g0315 a0005c0005t0005g0202 a0005c0095t0005g0199 |
3 | NA18963.hp2 NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.179-1913_179-1911d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81424884 | ||||||
| chr17:81424906 | G | T | 4 | a0003c0002t0001g0039 a0003c0002t0001g0095 a0003c0002t0001g0096 others(1): Show |
4 | NA18948.hp1 NA18966.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-1894G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424906 | |||||||
| chr17:81424917 | G | A | 2 | a0019c0030t0007g0032 a0019c0030t0007g0239 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-1883G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424917 | |||||||
| chr17:81424937 | G | T | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-1863G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424937 | |||||||
| chr17:81424960 | G | T | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-1840G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424960 | |||||||
| chr17:81424966 | TGTG | T | 3 | a0001c0001t0001g0278 a0002c0003t0003g0304 a0002c0009t0001g0255 |
3 | HG00544.hp1 NA18975.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.179-1831_179-1829d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81424966 | ||||||
| chr17:81424970 | G | T | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1830G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424970 | |||||||
| chr17:81424972 | T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1828T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424972 | |||||||
| chr17:81424989 | T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1811T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81424989 | |||||||
| chr17:81425045 | GGGTGATG others(8): Show |
G | 1 | a0001c0016t0001g0316 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.179-1737_179-1723d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425045 | ||||||
| chr17:81425117 | G | A | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-1683G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425117 | |||||||
| chr17:81425143 | T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1657T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425143 | |||||||
| chr17:81425150 | T | G | 41 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(38): Show |
42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.179-1650T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425150 | |||||||
| chr17:81425162 | T | A | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-1638T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425162 | |||||||
| chr17:81425164 | G | T | 1 | a0004c0004t0014g0190 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.179-1636G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425164 | |||||||
| chr17:81425170 | G | A | 1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1630G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425170 | |||||||
| chr17:81425171 | G | C | 1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1629G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425171 | |||||||
| chr17:81425172 | T | A | 1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1628T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425172 | |||||||
| chr17:81425172 | T | G | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-1628T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425172 | |||||||
| chr17:81425173 | G | C | 1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1627G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425173 | |||||||
| chr17:81425174 | G | T | 1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1626G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425174 | |||||||
| chr17:81425175 | T | A | 1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1625T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425175 | |||||||
| chr17:81425179 | A | C | 1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1621A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425179 | |||||||
| chr17:81425181 | T | C | 1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1619T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425181 | |||||||
| chr17:81425182 | GGTGGGTG others(41): Show |
G | 1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1617_179-1570d others(50): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425182 | |||||||
| chr17:81425202 | A | G | 51 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0276 others(48): Show |
52 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.179-1598A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425202 | |||||||
| chr17:81425205 | A | ATAG | 3 | a0001c0001t0001g0276 a0005c0005t0005g0202 a0010c0014t0001g0243 |
3 | HG00639.hp1 HG02723.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.179-1594_179-1593i others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425205 | ||||||
| chr17:81425207 | G | A | 48 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0321 others(45): Show |
49 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.179-1593G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425207 | |||||||
| chr17:81425209 | T | TGCTGGGT others(36): Show |
40 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(37): Show |
41 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.179-1590_179-1589i others(45): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425209 | ||||||
| chr17:81425209 | T | TGGGTGAT others(8): Show |
265 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.179-1590_179-1576d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425209 | ||||||
| chr17:81425209 | T | TGGGTGAT others(333): Show |
1 | a0002c0012t0002g0159 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.179-1576_179-1575i others(342): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425209 | ||||||
| chr17:81425209 | T | TGGTGGGT others(36): Show |
8 | a0001c0001t0001g0274 a0002c0010t0009g0014 a0002c0010t0016g0161 others(5): Show |
8 | HG02451.hp1 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-1589_179-1588i others(45): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425209 | ||||||
| chr17:81425221 | T | TTGGTGAT others(29): Show |
2 | a0001c0001t0001g0276 a0010c0014t0001g0243 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.179-1574_179-1573i others(38): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425221 | ||||||
| chr17:81425225 | T | G | 7 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-1575T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425225 | |||||||
| chr17:81425225 | T | TGATGATG others(3): Show |
1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.179-1574_179-1573i others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425225 | ||||||
| chr17:81425234 | G | T | 1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-1566G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425234 | |||||||
| chr17:81425236 | TTGGGGGT others(5): Show |
T | 7 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-1560_179-1549d others(14): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425236 | ||||||
| chr17:81425247 | A | G | 1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.179-1553A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425247 | |||||||
| chr17:81425248 | G | T | 1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.179-1552G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425248 | |||||||
| chr17:81425254 | A | G | 8 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1546A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425254 | |||||||
| chr17:81425281 | G | A | 8 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1519G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425281 | |||||||
| chr17:81425282 | G | T | 8 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1518G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425282 | |||||||
| chr17:81425283 | T | G | 8 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1517T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425283 | |||||||
| chr17:81425284 | G | A | 8 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1516G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425284 | |||||||
| chr17:81425288 | A | G | 8 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-1512A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425288 | |||||||
| chr17:81425305 | GTGGGTGA others(6): Show |
G | 1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.179-1490_179-1478d others(15): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425305 | ||||||
| chr17:81425311 | GA | G | 8 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-1488delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425311 | |||||||
| chr17:81425316 | G | A | 7 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-1484G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425316 | |||||||
| chr17:81425327 | ATAG | A | 5 | a0002c0009t0009g0185 a0012c0031t0004g0018 a0012c0102t0004g0017 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-1471_179-1469d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425327 | ||||||
| chr17:81425350 | T | G | 1 | a0004c0004t0002g0219 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.179-1450T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425350 | |||||||
| chr17:81425390 | TGGTGATA others(110): Show |
T | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-1380_179-1264d others(2): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425390 | ||||||
| chr17:81425398 | GTGGTGGG others(9): Show |
G | 1 | a0002c0003t0003g0230 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.179-1379_179-1364d others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425398 | ||||||
| chr17:81425404 | G | GGTGATGT others(7): Show |
88 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0276 others(85): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.179-1394_179-1381d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425404 | ||||||
| chr17:81425409 | T | TGTGGGTG others(6): Show |
1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1387_179-1386i others(15): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425409 | ||||||
| chr17:81425418 | TGG | T | 8 | a0002c0010t0009g0014 a0002c0010t0016g0161 a0002c0019t0003g0315 others(5): Show |
8 | HG02630.hp2 HG02965.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-1380_179-1379d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425418 | ||||||
| chr17:81425419 | GGGTGATG others(8): Show |
G | 1 | a0004c0011t0023g0041 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.179-1366_179-1352d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425419 | ||||||
| chr17:81425434 | T | TG | 6 | a0002c0019t0003g0315 a0002c0026t0003g0246 a0005c0005t0005g0202 others(3): Show |
6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1364dupG | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425434 | ||||||
| chr17:81425436 | GTGATGTG others(34): Show |
G | 2 | a0002c0010t0009g0014 a0002c0010t0016g0161 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.179-1363_179-1323d others(43): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425436 | |||||||
| chr17:81425444 | G | C | 2 | a0013c0027t0001g0024 a0013c0027t0001g0026 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.179-1356G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425444 | |||||||
| chr17:81425446 | T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1354T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425446 | |||||||
| chr17:81425449 | G | T | 6 | a0002c0019t0003g0315 a0002c0026t0003g0246 a0005c0005t0005g0202 others(3): Show |
6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1351G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425449 | |||||||
| chr17:81425455 | TA | T | 6 | a0002c0019t0003g0315 a0002c0026t0003g0246 a0005c0005t0005g0202 others(3): Show |
6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1344delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425455 | |||||||
| chr17:81425461 | T | TTGG | 6 | a0002c0019t0003g0315 a0002c0026t0003g0246 a0005c0005t0005g0202 others(3): Show |
6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1339_179-1338i others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425461 | |||||||
| chr17:81425463 | GGTGATGT others(7): Show |
G | 29 | a0001c0001t0002g0132 a0001c0062t0020g0252 a0002c0008t0025g0253 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.179-1321_179-1308d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425463 | ||||||
| chr17:81425468 | T | TA | 6 | a0002c0019t0003g0315 a0002c0026t0003g0246 a0005c0005t0005g0202 others(3): Show |
6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1332_179-1331i others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425468 | |||||||
| chr17:81425473 | TTG | T | 6 | a0002c0019t0003g0315 a0002c0026t0003g0246 a0005c0005t0005g0202 others(3): Show |
6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1326_179-1325d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425473 | |||||||
| chr17:81425477 | T | G | 6 | a0002c0019t0003g0315 a0002c0026t0003g0246 a0005c0005t0005g0202 others(3): Show |
6 | HG02965.hp2 HG03209.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1323T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425477 | |||||||
| chr17:81425477 | TGTGATGT others(9): Show |
T | 40 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(37): Show |
41 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.179-1309_179-1294d others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425477 | ||||||
| chr17:81425481 | A | G | 1 | a0002c0068t0007g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-1319A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425481 | |||||||
| chr17:81425491 | TGG | T | 5 | a0002c0019t0003g0315 a0002c0026t0003g0246 a0005c0005t0005g0202 others(2): Show |
5 | HG02965.hp2 NA18963.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-1307_179-1306d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425491 | ||||||
| chr17:81425531 | T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1269T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425531 | |||||||
| chr17:81425556 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.179-1244T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425556 | |||||||
| chr17:81425565 | TGGTGATG others(21): Show |
T | 1 | a0009c0072t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.179-1192_179-1165d others(30): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425565 | ||||||
| chr17:81425616 | G | C | 1 | a0002c0068t0007g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-1184G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425616 | |||||||
| chr17:81425625 | GATGTGGT others(8): Show |
G | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-1160_179-1146d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425625 | ||||||
| chr17:81425640 | T | G | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-1160T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425640 | |||||||
| chr17:81425640 | TATGTGGT others(8): Show |
T | 1 | a0002c0068t0007g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-1141_179-1127d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425640 | ||||||
| chr17:81425687 | T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1113T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425687 | |||||||
| chr17:81425711 | ATAG | A | 41 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(38): Show |
42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.179-1087_179-1085d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425711 | ||||||
| chr17:81425735 | GGTGATGT others(7): Show |
G | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-1049_179-1036d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425735 | ||||||
| chr17:81425759 | T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-1041T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425759 | |||||||
| chr17:81425765 | GTGATGTG others(8): Show |
G | 2 | a0013c0027t0001g0024 a0013c0027t0001g0026 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.179-1023_179-1009d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425765 | ||||||
| chr17:81425770 | G | C | 7 | a0001c0001t0002g0132 a0002c0093t0009g0015 a0004c0011t0002g0023 others(4): Show |
7 | HG02895.hp2 HG03017.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-1030G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425770 | |||||||
| chr17:81425812 | T | G | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-988T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425812 | |||||||
| chr17:81425882 | TGGTGATG others(9): Show |
T | 2 | a0013c0027t0001g0024 a0013c0027t0001g0026 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.179-909_179-894del others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425882 | ||||||
| chr17:81425905 | G | A | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-895G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425905 | |||||||
| chr17:81425907 | C | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-893C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425907 | |||||||
| chr17:81425908 | A | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-892A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425908 | |||||||
| chr17:81425910 | T | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-890T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425910 | |||||||
| chr17:81425921 | T | TTGGGGGT others(5): Show |
1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-876_179-875ins others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425921 | ||||||
| chr17:81425927 | C | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-873C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425927 | |||||||
| chr17:81425928 | A | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-872A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425928 | |||||||
| chr17:81425936 | A | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-864A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425936 | |||||||
| chr17:81425955 | G | A | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-845G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425955 | |||||||
| chr17:81425993 | T | TGGTGATA others(34): Show |
1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-806_179-805ins others(41): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81425993 | ||||||
| chr17:81425995 | A | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-805A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81425995 | |||||||
| chr17:81426000 | G | T | 41 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(38): Show |
42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.179-800G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426000 | |||||||
| chr17:81426016 | G | A | 1 | a0002c0003t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.179-784G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426016 | |||||||
| chr17:81426033 | T | TGGTGATA others(6): Show |
1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-761_179-760ins others(13): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426033 | ||||||
| chr17:81426044 | C | T | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-756C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426044 | |||||||
| chr17:81426046 | C | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-754C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426046 | |||||||
| chr17:81426048 | T | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-752T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426048 | |||||||
| chr17:81426053 | G | A | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-747G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426053 | |||||||
| chr17:81426055 | G | A | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-745G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426055 | |||||||
| chr17:81426055 | G | GGGGGGGG others(761): Show |
1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-744_179-743ins others(768): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426055 | ||||||
| chr17:81426055 | G | GGTGGTGG others(811): Show |
29 | a0001c0001t0002g0132 a0001c0062t0020g0252 a0002c0008t0025g0253 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(818): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426055 | ||||||
| chr17:81426055 | G | GGTGGTGG others(1771): Show |
1 | a0002c0050t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1778): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426055 | ||||||
| chr17:81426055 | G | GGTGGTGG others(811): Show |
1 | a0037c0089t0002g0265 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(818): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426055 | ||||||
| chr17:81426075 | G | GGGGTGAT others(6): Show |
1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-725_179-724ins others(13): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426075 | |||||||
| chr17:81426076 | T | G | 1 | a0003c0002t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-724T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426076 | |||||||
| chr17:81426076 | T | TGATGATG others(796): Show |
1 | a0001c0001t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.179-723_179-722ins others(803): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATA others(1698): Show |
1 | a0001c0001t0001g0004 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.179-718_179-717ins others(1705): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(796): Show |
1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(803): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(4000): Show |
3 | a0007c0007t0001g0005 a0007c0007t0001g0021 a0010c0014t0001g0001 |
4 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1713): Show |
1 | a0002c0003t0003g0314 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(2321): Show |
1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(2328): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(4081): Show |
1 | a0002c0026t0003g0246 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(4088): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(545): Show |
4 | a0016c0106t0010g0328 a0018c0105t0001g0250 a0028c0044t0001g0249 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(552): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1688): Show |
1 | a0004c0011t0023g0041 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1695): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(471): Show |
38 | a0001c0001t0001g0037 a0001c0001t0001g0108 a0001c0001t0001g0176 others(35): Show |
38 | HG00438.hp1 HG00741.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(478): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1698): Show |
1 | a0003c0002t0013g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1705): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1713): Show |
1 | a0056c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(796): Show |
6 | a0001c0001t0001g0320 a0003c0018t0001g0307 a0014c0022t0011g0322 others(3): Show |
6 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(803): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1712): Show |
1 | a0001c0001t0001g0244 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1719): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1670): Show |
1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1677): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(2182): Show |
1 | a0001c0001t0002g0141 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(2189): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1715): Show |
1 | a0002c0003t0003g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1722): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1713): Show |
146 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0035 others(143): Show |
147 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(2182): Show |
5 | a0001c0080t0001g0043 a0002c0008t0006g0134 a0004c0004t0002g0061 others(2): Show |
5 | HG01261.hp1 HG01928.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(2189): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1712): Show |
1 | a0038c0083t0003g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1719): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1710): Show |
4 | a0001c0001t0006g0149 a0001c0001t0007g0145 a0001c0061t0007g0152 others(1): Show |
4 | HG00738.hp1 HG02300.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(1717): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1685): Show |
2 | a0002c0032t0003g0232 a0035c0033t0001g0179 |
2 | HG01981.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.179-702_179-701ins others(1692): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1711): Show |
1 | a0003c0002t0004g0171 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1718): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1712): Show |
1 | a0027c0079t0004g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1719): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1713): Show |
1 | a0034c0069t0003g0116 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1713): Show |
1 | a0006c0006t0001g0151 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1713): Show |
1 | a0001c0001t0001g0223 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1698): Show |
1 | a0002c0012t0002g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1705): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(6192): Show |
1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(6199): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(2306): Show |
4 | a0002c0009t0009g0185 a0012c0031t0004g0018 a0012c0102t0004g0017 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(2313): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(2981): Show |
1 | a0002c0068t0007g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(2988): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(5562): Show |
1 | a0013c0027t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(5569): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(5478): Show |
1 | a0013c0027t0001g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(5485): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(471): Show |
1 | a0001c0043t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(478): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(3629): Show |
1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(3636): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(2704): Show |
1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(2711): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(5055): Show |
1 | a0002c0010t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(5062): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(3321): Show |
1 | a0002c0019t0003g0315 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(3328): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(3533): Show |
1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(3540): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(3321): Show |
1 | a0005c0095t0005g0199 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(3328): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1898): Show |
2 | a0019c0030t0007g0032 a0019c0030t0007g0239 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-702_179-701ins others(1905): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(4000): Show |
1 | a0007c0047t0002g0308 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(4000): Show |
4 | a0003c0002t0004g0310 a0007c0007t0001g0309 a0007c0007t0001g0312 others(1): Show |
4 | HG01243.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(3071): Show |
1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(3078): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1756): Show |
1 | a0005c0028t0001g0073 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(1763): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(2701): Show |
1 | a0009c0024t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(2708): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(4000): Show |
1 | a0004c0037t0014g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(4185): Show |
4 | a0001c0001t0001g0321 a0001c0075t0001g0303 a0002c0003t0003g0110 others(1): Show |
4 | HG02132.hp1 NA18947.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(4192): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(4000): Show |
1 | a0005c0005t0012g0204 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(4000): Show |
15 | a0001c0001t0001g0109 a0001c0001t0001g0324 a0001c0001t0001g0326 others(12): Show |
15 | HG01074.hp2 HG02165.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(4007): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(3997): Show |
4 | a0003c0002t0001g0124 a0003c0002t0001g0213 a0003c0002t0004g0122 others(1): Show |
4 | HG00423.hp2 HG00544.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-702_179-701ins others(4004): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(4241): Show |
1 | a0045c0057t0017g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(4248): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(3959): Show |
1 | a0002c0003t0003g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(3966): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(3999): Show |
1 | a0002c0010t0033g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(4006): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(2516): Show |
1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(2523): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(1534): Show |
1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1541): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(4004): Show |
1 | a0002c0008t0024g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(4011): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426076 | T | TGGTGATG others(2698): Show |
1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-702_179-701ins others(2705): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426076 | ||||||
| chr17:81426081 | A | ATGTGGTT others(1713): Show |
1 | a0001c0001t0001g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.179-702_179-701ins others(1720): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426081 | ||||||
| chr17:81426091 | T | TGGTGATA others(1685): Show |
2 | a0002c0003t0003g0286 a0002c0003t0003g0290 |
2 | NA18963.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.179-702_179-701ins others(1692): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426091 | ||||||
| chr17:81426099 | G | A | 5 | a0002c0003t0003g0289 a0002c0010t0009g0260 a0002c0010t0016g0234 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-701G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426099 | |||||||
| chr17:81426101 | G | T | 5 | a0002c0003t0003g0289 a0002c0010t0009g0260 a0002c0010t0016g0234 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-699G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426101 | |||||||
| chr17:81426105 | G | A | 4 | a0002c0009t0009g0185 a0012c0031t0004g0018 a0012c0102t0004g0017 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-695G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426105 | |||||||
| chr17:81426106 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-694G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426106 | |||||||
| chr17:81426119 | T | G | 5 | a0002c0003t0003g0289 a0002c0010t0009g0260 a0002c0010t0016g0234 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-681T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426119 | |||||||
| chr17:81426125 | TA | T | 321 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(318): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.179-674delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426125 | |||||||
| chr17:81426126 | A | AGTGGTGG others(2432): Show |
1 | a0017c0023t0015g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.179-669_179-668ins others(2439): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426126 | ||||||
| chr17:81426126 | A | AGTGGTGG others(2431): Show |
1 | a0002c0010t0009g0260 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.179-669_179-668ins others(2438): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426126 | ||||||
| chr17:81426126 | A | AGTGGTGG others(2548): Show |
1 | a0013c0096t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-669_179-668ins others(2555): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426126 | ||||||
| chr17:81426126 | A | AGTGGTGG others(2221): Show |
1 | a0002c0010t0016g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.179-669_179-668ins others(2228): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426126 | ||||||
| chr17:81426131 | T | TGGGTGAT others(1682): Show |
1 | a0002c0003t0003g0289 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.179-669_179-668ins others(1689): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426131 | |||||||
| chr17:81426152 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-648G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426152 | |||||||
| chr17:81426180 | A | G | 39 | a0001c0001t0001g0037 a0001c0001t0001g0108 a0001c0001t0001g0176 others(36): Show |
39 | HG00438.hp1 HG00609.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.179-620A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426180 | |||||||
| chr17:81426208 | A | ATGATGTG others(437): Show |
1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.179-548_179-547ins others(444): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426208 | ||||||
| chr17:81426208 | A | ATGATGTG others(438): Show |
30 | a0001c0001t0002g0132 a0001c0062t0020g0252 a0002c0008t0025g0253 others(27): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.179-548_179-547ins others(445): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426208 | ||||||
| chr17:81426253 | A | G | 48 | a0001c0001t0001g0037 a0001c0001t0001g0108 a0001c0001t0001g0176 others(45): Show |
49 | HG00438.hp1 HG00609.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.179-547A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426253 | |||||||
| chr17:81426284 | T | A | 44 | a0001c0001t0001g0037 a0001c0001t0001g0108 a0001c0001t0001g0176 others(41): Show |
44 | HG00438.hp1 HG00609.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.179-516T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426284 | |||||||
| chr17:81426284 | TGTG | T | 5 | a0002c0009t0009g0185 a0012c0031t0004g0018 a0012c0102t0004g0017 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-511_179-509del others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426284 | ||||||
| chr17:81426309 | G | T | 31 | a0001c0001t0002g0132 a0001c0062t0020g0252 a0002c0008t0025g0253 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.179-491G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426309 | |||||||
| chr17:81426333 | T | TGGTGATA others(49): Show |
38 | a0001c0001t0001g0037 a0001c0001t0001g0108 a0001c0001t0001g0176 others(35): Show |
38 | HG00438.hp1 HG00741.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.179-412_179-411ins others(56): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426333 | ||||||
| chr17:81426342 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-458T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426342 | |||||||
| chr17:81426344 | G | T | 1 | a0002c0068t0007g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179-456G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426344 | |||||||
| chr17:81426371 | G | GGTGGGTG others(221): Show |
1 | a0001c0043t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-412_179-411ins others(228): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426371 | ||||||
| chr17:81426389 | T | G | 1 | a0001c0043t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-411T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426389 | |||||||
| chr17:81426399 | C | G | 1 | a0001c0043t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-401C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426399 | |||||||
| chr17:81426445 | G | T | 1 | a0001c0043t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-355G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426445 | |||||||
| chr17:81426447 | G | T | 4 | a0002c0010t0009g0260 a0002c0010t0016g0234 a0013c0096t0001g0235 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-353G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426447 | |||||||
| chr17:81426451 | T | TAGCG | 4 | a0016c0106t0010g0328 a0018c0105t0001g0250 a0028c0044t0001g0249 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-349_179-348ins others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426451 | |||||||
| chr17:81426451 | T | TAGTCGTG others(5514): Show |
1 | a0001c0043t0001g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.179-349_179-348ins others(5521): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426451 | |||||||
| chr17:81426451 | T | TAGTG | 94 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0276 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.179-349_179-348ins others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426451 | |||||||
| chr17:81426451 | T | TAGTGGTG others(262): Show |
2 | a0019c0030t0007g0032 a0019c0030t0007g0239 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-349_179-348ins others(269): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426451 | |||||||
| chr17:81426451 | T | TAGTGGTG others(832): Show |
1 | a0002c0050t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-349_179-348ins others(839): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426451 | |||||||
| chr17:81426489 | A | G | 1 | a0002c0050t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-311A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426489 | |||||||
| chr17:81426493 | C | T | 1 | a0002c0050t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-307C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426493 | |||||||
| chr17:81426495 | C | G | 1 | a0002c0050t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-305C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426495 | |||||||
| chr17:81426511 | G | A | 1 | a0002c0050t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-289G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426511 | |||||||
| chr17:81426515 | T | TGTGGTTG others(1565): Show |
1 | a0002c0050t0001g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.179-282_179-281ins others(1572): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | 81426515 | ||||||
| chr17:81426682 | T | C | 184 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0033 others(181): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.179-118T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426682 | |||||||
| chr17:81426683 | G | C | 1 | a0005c0005t0012g0206 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.179-117G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | chr17 | 81426683 | |||||||
| chr17:81427077 | G | A | 3 | a0002c0012t0002g0058 a0002c0012t0002g0159 a0015c0015t0001g0166 |
3 | HG01346.hp2 HG02451.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.358+98G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427077 | |||||||
| chr17:81427089 | C | T | 2 | a0003c0063t0005g0198 a0053c0070t0003g0006 |
2 | NA18966.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.358+110C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427089 | |||||||
| chr17:81427115 | G | A | 2 | a0001c0001t0001g0276 a0010c0014t0001g0243 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.358+136G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427115 | |||||||
| chr17:81427156 | G | A | 5 | a0002c0012t0002g0112 a0005c0005t0012g0204 a0005c0005t0012g0206 others(2): Show |
5 | HG03239.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+177G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427156 | |||||||
| chr17:81427173 | A | G | 1 | a0003c0002t0001g0107 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.358+194A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427173 | |||||||
| chr17:81427186 | C | T | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.358+207C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427186 | |||||||
| chr17:81427236 | CAG | C | 4 | a0002c0009t0009g0185 a0002c0093t0009g0015 a0012c0031t0004g0016 others(1): Show |
4 | HG02622.hp1 HG02895.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+258_358+259del others(2): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427236 | |||||||
| chr17:81427365 | C | G | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.358+386C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427365 | |||||||
| chr17:81427489 | A | G | 108 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0276 others(105): Show |
109 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.358+510A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427489 | |||||||
| chr17:81427507 | G | A | 4 | a0002c0003t0003g0314 a0002c0093t0009g0015 a0012c0031t0004g0016 others(1): Show |
4 | HG02895.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+528G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427507 | |||||||
| chr17:81427553 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.358+574G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427553 | |||||||
| chr17:81427651 | C | T | 1 | a0003c0002t0013g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.358+672C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427651 | |||||||
| chr17:81427697 | A | C | 3 | a0005c0005t0012g0204 a0005c0005t0012g0206 a0005c0005t0012g0207 |
3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.358+718A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427697 | |||||||
| chr17:81427708 | G | A | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.358+729G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427708 | |||||||
| chr17:81427749 | G | A | 4 | a0002c0003t0003g0067 a0004c0004t0002g0167 a0004c0004t0002g0240 others(1): Show |
4 | HG00642.hp1 HG01167.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+770G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427749 | |||||||
| chr17:81427858 | C | T | 1 | a0002c0068t0007g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.358+879C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427858 | |||||||
| chr17:81427860 | C | T | 1 | a0001c0001t0006g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.358+881C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427860 | |||||||
| chr17:81427864 | G | A | 8 | a0001c0001t0001g0242 a0001c0001t0002g0132 a0001c0080t0001g0043 others(5): Show |
8 | HG02280.hp1 HG02698.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+885G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427864 | |||||||
| chr17:81427881 | C | T | 3 | a0001c0001t0001g0276 a0003c0002t0013g0025 a0010c0014t0001g0243 |
3 | HG00639.hp1 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.358+902C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427881 | |||||||
| chr17:81427889 | C | T | 38 | a0001c0001t0001g0109 a0001c0001t0001g0321 a0001c0001t0001g0324 others(35): Show |
39 | HG00423.hp2 HG00544.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.358+910C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427889 | |||||||
| chr17:81427953 | A | G | 15 | a0001c0001t0001g0321 a0001c0043t0001g0164 a0001c0075t0001g0303 others(12): Show |
15 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.358+974A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81427953 | |||||||
| chr17:81428175 | C | T | 125 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0108 others(122): Show |
125 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.358+1196C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428175 | |||||||
| chr17:81428241 | G | A | 2 | a0001c0001t0001g0276 a0010c0014t0001g0243 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.358+1262G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428241 | |||||||
| chr17:81428306 | A | C | 7 | a0001c0001t0001g0224 a0001c0001t0007g0090 a0002c0003t0003g0068 others(4): Show |
7 | HG00323.hp1 HG00639.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1327A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428306 | |||||||
| chr17:81428362 | C | T | 1 | a0002c0068t0007g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.358+1383C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428362 | |||||||
| chr17:81428484 | G | A | 2 | a0001c0001t0001g0276 a0010c0014t0001g0243 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.358+1505G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428484 | |||||||
| chr17:81428522 | C | T | 2 | a0019c0030t0007g0032 a0019c0030t0007g0239 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.358+1543C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428522 | |||||||
| chr17:81428534 | C | G | 22 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0002g0132 others(19): Show |
23 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.358+1555C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428534 | |||||||
| chr17:81428552 | C | G | 7 | a0001c0062t0020g0252 a0002c0008t0024g0248 a0002c0008t0025g0253 others(4): Show |
7 | HG01261.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1573C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428552 | |||||||
| chr17:81428661 | C | A | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.358+1682C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428661 | |||||||
| chr17:81428762 | C | T | 2 | a0001c0043t0001g0164 a0002c0085t0003g0031 |
2 | HG00609.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.358+1783C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428762 | |||||||
| chr17:81428830 | C | T | 9 | a0001c0001t0002g0132 a0002c0068t0007g0254 a0002c0093t0009g0015 others(6): Show |
9 | HG02451.hp1 HG02895.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.358+1851C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428830 | |||||||
| chr17:81428858 | C | T | 16 | a0001c0001t0001g0109 a0002c0009t0001g0034 a0002c0010t0033g0135 others(13): Show |
17 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.358+1879C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428858 | |||||||
| chr17:81428896 | A | G | 18 | a0001c0001t0001g0109 a0002c0009t0001g0034 a0002c0010t0009g0014 others(15): Show |
19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.358+1917A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428896 | |||||||
| chr17:81428915 | G | A | 7 | a0001c0001t0001g0274 a0001c0001t0001g0324 a0001c0001t0001g0326 others(4): Show |
7 | HG01074.hp2 HG02559.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1936G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81428915 | |||||||
| chr17:81429125 | T | G | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358+2146T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429125 | |||||||
| chr17:81429165 | C | T | 1 | a0002c0025t0003g0065 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.358+2186C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429165 | |||||||
| chr17:81429187 | A | G | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358+2208A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429187 | |||||||
| chr17:81429188 | G | T | 18 | a0002c0008t0037g0319 a0002c0010t0009g0260 a0002c0010t0016g0234 others(15): Show |
19 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.358+2209G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429188 | |||||||
| chr17:81429310 | C | G | 7 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+2331C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429310 | |||||||
| chr17:81429338 | C | G | 2 | a0002c0003t0003g0053 a0035c0033t0001g0179 |
2 | HG02523.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.358+2359C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429338 | |||||||
| chr17:81429446 | C | T | 1 | a0001c0055t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.358+2467C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429446 | |||||||
| chr17:81429477 | G | A | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.358+2498G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429477 | |||||||
| chr17:81429518 | T | A | 1 | a0009c0024t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.358+2539T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429518 | |||||||
| chr17:81429552 | C | A | 1 | a0003c0002t0013g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358+2573C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429552 | |||||||
| chr17:81429751 | A | AC | 5 | a0001c0001t0002g0130 a0001c0016t0001g0052 a0001c0051t0001g0045 others(2): Show |
5 | HG01433.hp1 HG02135.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+2777dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81429751 | ||||||
| chr17:81429751 | A | G | 1 | a0002c0012t0002g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.358+2772A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429751 | |||||||
| chr17:81429855 | C | T | 3 | a0002c0010t0009g0014 a0002c0010t0016g0161 a0036c0045t0004g0273 |
3 | HG02630.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.358+2876C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429855 | |||||||
| chr17:81429857 | G | T | 7 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+2878G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429857 | |||||||
| chr17:81429973 | G | A | 1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.358+2994G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429973 | |||||||
| chr17:81429983 | G | A | 1 | a0037c0089t0002g0265 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.358+3004G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81429983 | |||||||
| chr17:81430002 | G | A | 1 | a0041c0107t0002g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.358+3023G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430002 | |||||||
| chr17:81430022 | C | A | 2 | a0019c0030t0007g0032 a0019c0030t0007g0239 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.358+3043C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430022 | |||||||
| chr17:81430027 | T | C | 45 | a0001c0001t0001g0109 a0001c0001t0002g0132 a0001c0062t0020g0252 others(42): Show |
46 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.358+3048T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430027 | |||||||
| chr17:81430030 | C | A | 16 | a0001c0001t0001g0109 a0002c0009t0001g0034 a0002c0010t0033g0135 others(13): Show |
17 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.358+3051C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430030 | |||||||
| chr17:81430219 | C | G | 1 | a0002c0003t0003g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.358+3240C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430219 | |||||||
| chr17:81430341 | C | T | 1 | a0006c0006t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.358+3362C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430341 | |||||||
| chr17:81430394 | G | A | 8 | a0002c0003t0010g0211 a0002c0012t0002g0133 a0002c0021t0002g0088 others(5): Show |
8 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+3415G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430394 | |||||||
| chr17:81430408 | C | T | 4 | a0002c0010t0009g0260 a0002c0010t0016g0161 a0017c0023t0015g0277 others(1): Show |
4 | HG02630.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+3429C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430408 | |||||||
| chr17:81430552 | C | T | 4 | a0004c0037t0014g0256 a0016c0106t0010g0328 a0018c0105t0001g0250 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+3573C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430552 | |||||||
| chr17:81430656 | C | T | 1 | a0009c0072t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.358+3677C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430656 | |||||||
| chr17:81430668 | C | T | 12 | a0002c0003t0003g0186 a0004c0004t0002g0092 a0004c0004t0002g0093 others(9): Show |
12 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.358+3689C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430668 | |||||||
| chr17:81430716 | T | C | 1 | a0002c0084t0001g0070 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.358+3737T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430716 | |||||||
| chr17:81430763 | C | T | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.358+3784C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430763 | |||||||
| chr17:81430802 | G | A | 4 | a0004c0037t0014g0256 a0016c0106t0010g0328 a0028c0044t0001g0249 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+3823G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430802 | |||||||
| chr17:81430839 | C | T | 21 | a0002c0008t0037g0319 a0003c0018t0002g0144 a0004c0004t0002g0003 others(18): Show |
22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.358+3860C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430839 | |||||||
| chr17:81430965 | G | A | 29 | a0002c0008t0037g0319 a0002c0010t0009g0260 a0002c0010t0016g0234 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.358+3986G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81430965 | |||||||
| chr17:81430984 | CCGGCGTG others(27): Show |
C | 10 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0324 others(7): Show |
10 | HG00639.hp1 HG01074.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.358+4039_358+4072d others(36): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81430984 | ||||||
| chr17:81431018 | TCGGCGTG others(27): Show |
T | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.358+4070_358+4103d others(36): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81431018 | ||||||
| chr17:81431090 | C | T | 1 | a0009c0024t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.358+4111C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431090 | |||||||
| chr17:81431091 | G | A | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.358+4112G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431091 | |||||||
| chr17:81431097 | G | A | 8 | a0002c0003t0010g0211 a0002c0012t0002g0133 a0002c0021t0002g0088 others(5): Show |
8 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+4118G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431097 | |||||||
| chr17:81431118 | G | A | 2 | a0005c0005t0005g0202 a0005c0095t0005g0199 |
2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.358+4139G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431118 | |||||||
| chr17:81431185 | C | T | 1 | a0004c0004t0002g0156 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.358+4206C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431185 | |||||||
| chr17:81431186 | G | A | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358+4207G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431186 | |||||||
| chr17:81431265 | T | TGCCA | 4 | a0001c0001t0001g0320 a0014c0022t0011g0322 a0014c0022t0011g0323 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+4288_358+4291d others(6): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81431265 | ||||||
| chr17:81431271 | G | C | 27 | a0001c0001t0001g0109 a0002c0003t0010g0211 a0002c0009t0001g0034 others(24): Show |
28 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.358+4292G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431271 | |||||||
| chr17:81431283 | C | T | 8 | a0001c0001t0002g0132 a0002c0068t0007g0254 a0002c0093t0009g0015 others(5): Show |
8 | HG02451.hp1 HG02895.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.358+4304C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431283 | |||||||
| chr17:81431324 | A | G | 131 | a0001c0001t0001g0109 a0001c0001t0001g0131 a0001c0001t0001g0244 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.358+4345A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431324 | |||||||
| chr17:81431325 | A | G | 4 | a0003c0002t0001g0039 a0003c0002t0001g0095 a0003c0002t0001g0096 others(1): Show |
4 | NA18948.hp1 NA18966.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+4346A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431325 | |||||||
| chr17:81431349 | GCAT | G | 71 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0276 others(68): Show |
73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.358+4371_358+4373d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431349 | |||||||
| chr17:81431545 | T | C | 1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.358+4566T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431545 | |||||||
| chr17:81431560 | C | A | 1 | a0002c0021t0002g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.358+4581C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431560 | |||||||
| chr17:81431607 | A | C | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358+4628A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431607 | |||||||
| chr17:81431623 | T | G | 24 | a0001c0001t0001g0109 a0002c0003t0010g0211 a0002c0009t0001g0034 others(21): Show |
25 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.358+4644T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431623 | |||||||
| chr17:81431702 | C | T | 2 | a0002c0010t0009g0014 a0002c0010t0016g0161 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.358+4723C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431702 | |||||||
| chr17:81431719 | C | T | 2 | a0016c0106t0010g0328 a0018c0105t0001g0250 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.358+4740C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431719 | |||||||
| chr17:81431777 | C | G | 31 | a0002c0008t0037g0319 a0002c0010t0009g0260 a0002c0010t0016g0234 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.358+4798C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431777 | |||||||
| chr17:81431801 | G | C | 27 | a0001c0001t0001g0109 a0002c0003t0010g0211 a0002c0009t0001g0034 others(24): Show |
28 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.358+4822G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431801 | |||||||
| chr17:81431837 | C | T | 1 | a0002c0025t0003g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.358+4858C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431837 | |||||||
| chr17:81431931 | G | A | 11 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0002c0008t0004g0117 others(8): Show |
11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+4952G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431931 | |||||||
| chr17:81431968 | C | T | 24 | a0001c0001t0001g0109 a0002c0003t0010g0211 a0002c0009t0001g0034 others(21): Show |
25 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.358+4989C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431968 | |||||||
| chr17:81431975 | G | A | 4 | a0001c0001t0001g0131 a0002c0003t0003g0067 a0002c0003t0003g0186 others(1): Show |
4 | HG01361.hp1 HG01515.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+4996G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81431975 | |||||||
| chr17:81432210 | G | A | 1 | a0004c0004t0002g0218 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.358+5231G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432210 | |||||||
| chr17:81432260 | G | A | 2 | a0001c0001t0001g0136 a0003c0002t0004g0205 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.358+5281G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432260 | |||||||
| chr17:81432357 | G | A | 1 | a0002c0010t0009g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.358+5378G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432357 | |||||||
| chr17:81432477 | G | A | 2 | a0002c0010t0009g0014 a0002c0010t0016g0161 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.358+5498G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432477 | |||||||
| chr17:81432481 | ACTGTCCA others(28): Show |
A | 1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.358+5503_358+5537d others(37): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432481 | |||||||
| chr17:81432508 | G | A | 1 | a0056c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.358+5529G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432508 | |||||||
| chr17:81432544 | A | ATCAGGCC others(17): Show |
15 | a0001c0001t0001g0109 a0002c0009t0001g0034 a0002c0010t0033g0135 others(12): Show |
16 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.358+5565_358+5566i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432544 | |||||||
| chr17:81432545 | C | T | 1 | a0003c0002t0013g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358+5566C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432545 | |||||||
| chr17:81432547 | A | AGGCCCAC others(17): Show |
54 | a0001c0001t0002g0132 a0002c0003t0010g0211 a0002c0008t0037g0319 others(51): Show |
55 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.358+5582_358+5605d others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432547 | ||||||
| chr17:81432547 | A | AGGCCCAC others(42): Show |
1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.358+5597_358+5598i others(51): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432547 | ||||||
| chr17:81432547 | A | G | 15 | a0001c0001t0001g0109 a0002c0009t0001g0034 a0002c0010t0033g0135 others(12): Show |
16 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.358+5568A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432547 | |||||||
| chr17:81432557 | T | TCCCTCCC others(37): Show |
15 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0285 others(12): Show |
15 | HG01361.hp1 HG02155.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.358+5605_358+5606i others(46): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432557 | ||||||
| chr17:81432557 | T | TCCCTCCC others(61): Show |
26 | a0001c0001t0001g0131 a0001c0001t0001g0244 a0001c0001t0001g0324 others(23): Show |
26 | HG00639.hp1 HG00673.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.358+5605_358+5606i others(70): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432557 | ||||||
| chr17:81432557 | T | TCCCTCCC others(105): Show |
1 | a0001c0062t0020g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.358+5605_358+5606i others(114): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432557 | ||||||
| chr17:81432557 | T | TCCCTCCC others(85): Show |
3 | a0012c0031t0004g0018 a0012c0102t0004g0017 a0018c0036t0001g0019 |
3 | HG02258.hp2 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.358+5605_358+5606i others(94): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432557 | ||||||
| chr17:81432557 | T | TCCCTCCC others(62): Show |
1 | a0002c0003t0003g0289 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.358+5605_358+5606i others(71): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432557 | ||||||
| chr17:81432570 | C | CGGGCCCA others(17): Show |
2 | a0005c0005t0005g0202 a0005c0095t0005g0199 |
2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.358+5605_358+5606i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432570 | ||||||
| chr17:81432697 | G | GCATCCCC others(41): Show |
1 | a0002c0003t0003g0300 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.359-5651_359-5650i others(50): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432697 | ||||||
| chr17:81432697 | G | GCATCCCC others(17): Show |
1 | a0005c0065t0034g0313 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.359-5652_359-5651i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432697 | ||||||
| chr17:81432720 | G | C | 2 | a0002c0003t0003g0300 a0005c0065t0034g0313 |
2 | HG03942.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.359-5650G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432720 | |||||||
| chr17:81432720 | G | GCCATCCC others(17): Show |
297 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(294): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.359-5640_359-5639i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432720 | ||||||
| chr17:81432720 | G | GCCATCCC others(18): Show |
4 | a0003c0002t0001g0105 a0003c0002t0001g0106 a0003c0002t0001g0213 others(1): Show |
4 | HG01928.hp1 HG02080.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-5640_359-5639i others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432720 | ||||||
| chr17:81432720 | G | GCCATCCC others(17): Show |
2 | a0001c0016t0001g0052 a0001c0051t0001g0045 |
2 | NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.359-5640_359-5639i others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432720 | ||||||
| chr17:81432729 | A | AGGCCCAC others(18): Show |
1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-5640_359-5639i others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432729 | ||||||
| chr17:81432731 | A | G | 16 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0002c0003t0003g0286 others(13): Show |
16 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.359-5639A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432731 | |||||||
| chr17:81432736 | C | CCCTCCCC others(16): Show |
1 | a0002c0003t0003g0289 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.359-5625_359-5624i others(25): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432736 | ||||||
| chr17:81432743 | CCCGAGCC others(17): Show |
C | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-5624_359-5601d others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432743 | ||||||
| chr17:81432746 | G | C | 13 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0002c0003t0003g0286 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.359-5624G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432746 | |||||||
| chr17:81432748 | G | T | 13 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0002c0003t0003g0286 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.359-5622G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432748 | |||||||
| chr17:81432766 | C | CCCCGAGC others(66): Show |
7 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0003c0002t0004g0170 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-5604_359-5603i others(75): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432766 | |||||||
| chr17:81432767 | T | C | 13 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0002c0003t0003g0286 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.359-5603T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432767 | |||||||
| chr17:81432770 | C | G | 5 | a0002c0010t0009g0014 a0002c0010t0016g0161 a0003c0002t0013g0025 others(2): Show |
5 | HG02630.hp2 HG03486.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-5600C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432770 | |||||||
| chr17:81432772 | T | G | 6 | a0002c0003t0003g0286 a0002c0010t0009g0014 a0002c0010t0016g0161 others(3): Show |
6 | HG02630.hp2 HG03486.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-5598T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432772 | |||||||
| chr17:81432779 | G | A | 7 | a0002c0003t0003g0286 a0002c0010t0009g0014 a0002c0010t0016g0161 others(4): Show |
7 | HG02630.hp2 HG02976.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-5591G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432779 | |||||||
| chr17:81432791 | C | T | 6 | a0002c0003t0003g0286 a0002c0010t0009g0014 a0002c0010t0016g0161 others(3): Show |
6 | HG02630.hp2 HG03486.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-5579C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432791 | |||||||
| chr17:81432793 | CA | C | 8 | a0002c0003t0003g0286 a0002c0010t0009g0014 a0002c0010t0016g0161 others(5): Show |
8 | HG02630.hp2 HG02976.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.359-5576delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432793 | |||||||
| chr17:81432795 | C | G | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-5575C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432795 | |||||||
| chr17:81432797 | T | G | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-5573T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432797 | |||||||
| chr17:81432804 | G | A | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.359-5566G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432804 | |||||||
| chr17:81432815 | G | C | 37 | a0002c0003t0003g0286 a0002c0008t0037g0319 a0002c0010t0009g0014 others(34): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.359-5555G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432815 | |||||||
| chr17:81432815 | G | GCCCCATC others(65): Show |
11 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0002c0008t0004g0117 others(8): Show |
11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-5543_359-5542i others(74): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432815 | ||||||
| chr17:81432815 | G | GCCCCATC others(18): Show |
1 | a0001c0001t0002g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.359-5533_359-5509d others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432815 | ||||||
| chr17:81432818 | C | CA | 37 | a0002c0003t0003g0286 a0002c0008t0037g0319 a0002c0010t0009g0014 others(34): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.359-5552_359-5551i others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432818 | |||||||
| chr17:81432833 | C | CCCTCCCC others(42): Show |
2 | a0002c0012t0002g0112 a0045c0057t0017g0191 |
2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.359-5492_359-5444d others(51): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432833 | ||||||
| chr17:81432836 | TC | T | 37 | a0002c0003t0003g0286 a0002c0008t0037g0319 a0002c0010t0009g0014 others(34): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.359-5526delC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432836 | ||||||
| chr17:81432840 | C | G | 37 | a0002c0003t0003g0286 a0002c0008t0037g0319 a0002c0010t0009g0014 others(34): Show |
38 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.359-5530C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432840 | |||||||
| chr17:81432842 | C | T | 1 | a0001c0055t0001g0038 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.359-5528C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432842 | |||||||
| chr17:81432843 | C | A | 11 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0002c0008t0004g0117 others(8): Show |
11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-5527C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432843 | |||||||
| chr17:81432857 | A | C | 9 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0324 others(6): Show |
9 | HG01074.hp2 HG02559.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.359-5513A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432857 | |||||||
| chr17:81432861 | T | TC | 43 | a0001c0001t0002g0132 a0002c0008t0037g0319 a0002c0010t0009g0014 others(40): Show |
44 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.359-5509_359-5508i others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432861 | |||||||
| chr17:81432862 | T | C | 56 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0132 others(53): Show |
57 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.359-5508T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432862 | |||||||
| chr17:81432864 | C | G | 11 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0002c0008t0004g0117 others(8): Show |
11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-5506C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432864 | |||||||
| chr17:81432872 | C | T | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.359-5498C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432872 | |||||||
| chr17:81432882 | A | C | 53 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0001c0001t0002g0132 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.359-5488A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432882 | |||||||
| chr17:81432885 | TC | T | 42 | a0001c0001t0002g0132 a0002c0003t0003g0286 a0002c0008t0037g0319 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.359-5477delC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432885 | ||||||
| chr17:81432887 | C | T | 42 | a0001c0001t0002g0132 a0002c0003t0003g0286 a0002c0008t0037g0319 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.359-5483C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432887 | |||||||
| chr17:81432887 | CCCCCCCA others(17): Show |
C | 75 | a0001c0001t0001g0109 a0001c0001t0001g0131 a0001c0001t0001g0244 others(72): Show |
76 | HG00099.hp2 HG00639.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.359-5467_359-5444d others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432887 | ||||||
| chr17:81432888 | CCCCCCAT others(16): Show |
C | 1 | a0008c0013t0006g0072 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.359-5476_359-5454d others(25): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432888 | ||||||
| chr17:81432891 | C | A | 1 | a0011c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.359-5479C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432891 | |||||||
| chr17:81432892 | C | G | 9 | a0001c0001t0001g0136 a0001c0001t0001g0169 a0001c0001t0001g0174 others(6): Show |
9 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.359-5478C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432892 | |||||||
| chr17:81432907 | C | A | 42 | a0001c0001t0002g0132 a0002c0003t0003g0286 a0002c0008t0037g0319 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.359-5463C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432907 | |||||||
| chr17:81432909 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.359-5461C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432909 | |||||||
| chr17:81432910 | T | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(98): Show |
103 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.359-5460T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432910 | |||||||
| chr17:81432910 | T | TC | 40 | a0001c0001t0002g0132 a0002c0003t0003g0286 a0002c0008t0037g0319 others(37): Show |
41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.359-5460_359-5459i others(3): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432910 | |||||||
| chr17:81432911 | T | C | 42 | a0001c0001t0002g0132 a0002c0003t0003g0286 a0002c0008t0037g0319 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.359-5459T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81432911 | |||||||
| chr17:81432911 | T | TCCCCCCA others(18): Show |
10 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0002c0008t0004g0117 others(7): Show |
10 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.359-5444_359-5443i others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432911 | ||||||
| chr17:81432917 | C | CATCCCCA others(18): Show |
1 | a0006c0020t0002g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.359-5444_359-5443i others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81432917 | ||||||
| chr17:81433072 | G | A | 1 | a0002c0003t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.359-5298G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433072 | |||||||
| chr17:81433133 | G | C | 18 | a0001c0001t0001g0109 a0001c0001t0001g0276 a0002c0009t0001g0034 others(15): Show |
19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.359-5237G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433133 | |||||||
| chr17:81433216 | G | C | 36 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0001t0001g0223 others(33): Show |
36 | HG00544.hp2 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.359-5154G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433216 | |||||||
| chr17:81433423 | T | C | 21 | a0001c0001t0001g0279 a0001c0001t0001g0281 a0001c0001t0001g0282 others(18): Show |
22 | HG00408.hp1 HG01069.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.359-4947T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433423 | |||||||
| chr17:81433510 | T | C | 1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4860T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433510 | |||||||
| chr17:81433523 | A | C | 1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4847A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433523 | |||||||
| chr17:81433554 | T | C | 1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-4816T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433554 | |||||||
| chr17:81433562 | T | C | 1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4808T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433562 | |||||||
| chr17:81433563 | T | C | 1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4807T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433563 | |||||||
| chr17:81433564 | A | C | 1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4806A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433564 | |||||||
| chr17:81433576 | A | G | 1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4794A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433576 | |||||||
| chr17:81433595 | C | T | 10 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0002c0008t0004g0117 others(7): Show |
10 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.359-4775C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433595 | |||||||
| chr17:81433671 | G | A | 2 | a0013c0027t0001g0024 a0013c0027t0001g0026 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.359-4699G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433671 | |||||||
| chr17:81433708 | G | A | 1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.359-4662G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433708 | |||||||
| chr17:81433727 | G | A | 6 | a0001c0001t0001g0169 a0003c0002t0004g0170 a0003c0002t0004g0171 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-4643G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433727 | |||||||
| chr17:81433748 | C | T | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-4622C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433748 | |||||||
| chr17:81433757 | C | T | 17 | a0001c0001t0001g0109 a0001c0001t0001g0174 a0002c0009t0001g0034 others(14): Show |
18 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.359-4613C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433757 | |||||||
| chr17:81433869 | A | G | 4 | a0002c0093t0009g0015 a0010c0014t0001g0243 a0019c0030t0007g0032 others(1): Show |
4 | HG00639.hp1 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-4501A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433869 | |||||||
| chr17:81433990 | G | A | 7 | a0002c0003t0010g0211 a0002c0012t0002g0133 a0002c0021t0002g0088 others(4): Show |
7 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-4380G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81433990 | |||||||
| chr17:81434023 | C | T | 3 | a0001c0001t0002g0132 a0008c0013t0006g0029 a0008c0013t0006g0140 |
3 | HG03017.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.359-4347C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434023 | |||||||
| chr17:81434070 | C | T | 2 | a0005c0005t0005g0202 a0005c0095t0005g0199 |
2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.359-4300C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434070 | |||||||
| chr17:81434216 | C | T | 10 | a0002c0003t0010g0211 a0002c0012t0002g0133 a0002c0021t0002g0088 others(7): Show |
10 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.359-4154C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434216 | |||||||
| chr17:81434248 | C | T | 1 | a0006c0020t0002g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.359-4122C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434248 | |||||||
| chr17:81434291 | A | T | 7 | a0002c0003t0010g0211 a0002c0012t0002g0133 a0002c0021t0002g0088 others(4): Show |
7 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-4079A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434291 | |||||||
| chr17:81434313 | C | T | 1 | a0013c0096t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.359-4057C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434313 | |||||||
| chr17:81434355 | G | A | 3 | a0001c0001t0001g0320 a0014c0022t0011g0322 a0014c0022t0011g0323 |
3 | HG01884.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.359-4015G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434355 | |||||||
| chr17:81434365 | C | T | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-4005C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434365 | |||||||
| chr17:81434396 | A | G | 7 | a0002c0003t0010g0211 a0002c0012t0002g0133 a0002c0021t0002g0088 others(4): Show |
7 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-3974A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434396 | |||||||
| chr17:81434413 | G | A | 1 | a0003c0002t0004g0122 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.359-3957G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434413 | |||||||
| chr17:81434447 | G | T | 1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-3923G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434447 | |||||||
| chr17:81434463 | C | T | 1 | a0007c0007t0001g0257 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.359-3907C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434463 | |||||||
| chr17:81434487 | G | A | 1 | a0008c0013t0006g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.359-3883G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434487 | |||||||
| chr17:81434656 | C | T | 3 | a0002c0068t0007g0254 a0012c0031t0004g0016 a0037c0089t0002g0265 |
3 | HG02451.hp1 HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.359-3714C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434656 | |||||||
| chr17:81434739 | C | A | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-3631C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434739 | |||||||
| chr17:81434741 | G | C | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-3629G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434741 | |||||||
| chr17:81434744 | T | G | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-3626T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434744 | |||||||
| chr17:81434906 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.359-3464C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434906 | |||||||
| chr17:81434946 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.359-3424C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81434946 | |||||||
| chr17:81435036 | C | G | 1 | a0056c0104t0010g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.359-3334C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435036 | |||||||
| chr17:81435107 | A | G | 1 | a0005c0005t0008g0297 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.359-3263A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435107 | |||||||
| chr17:81435117 | A | C | 1 | a0004c0004t0002g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.359-3253A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435117 | |||||||
| chr17:81435142 | C | T | 1 | a0001c0016t0001g0316 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.359-3228C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435142 | |||||||
| chr17:81435219 | G | A | 2 | a0002c0010t0009g0014 a0002c0010t0016g0161 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.359-3151G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435219 | |||||||
| chr17:81435347 | G | A | 16 | a0001c0001t0001g0109 a0002c0009t0001g0034 a0002c0010t0033g0135 others(13): Show |
17 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.359-3023G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435347 | |||||||
| chr17:81435389 | A | C | 1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-2981A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435389 | |||||||
| chr17:81435399 | G | A | 1 | a0041c0107t0002g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.359-2971G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435399 | |||||||
| chr17:81435402 | C | T | 2 | a0019c0030t0007g0032 a0019c0030t0007g0239 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.359-2968C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435402 | |||||||
| chr17:81435458 | G | C | 1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-2912G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435458 | |||||||
| chr17:81435488 | C | T | 32 | a0001c0001t0001g0131 a0001c0001t0001g0244 a0001c0001t0001g0285 others(29): Show |
32 | HG00673.hp1 HG01109.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.359-2882C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435488 | |||||||
| chr17:81435577 | C | T | 11 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0002c0008t0004g0117 others(8): Show |
11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-2793C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435577 | |||||||
| chr17:81435672 | G | A | 1 | a0010c0014t0001g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.359-2698G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435672 | |||||||
| chr17:81435756 | A | C | 1 | a0001c0001t0005g0064 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.359-2614A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435756 | |||||||
| chr17:81435923 | C | A | 2 | a0002c0008t0024g0248 a0002c0008t0025g0253 |
2 | HG01261.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.359-2447C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81435923 | |||||||
| chr17:81435937 | CTTTCTCA others(3): Show |
C | 1 | a0011c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.359-2430_359-2421d others(12): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr17 | 81435937 | ||||||
| chr17:81436058 | G | C | 2 | a0002c0103t0026g0245 a0007c0007t0004g0317 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.359-2312G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436058 | |||||||
| chr17:81436135 | T | C | 74 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0276 others(71): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.359-2235T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436135 | |||||||
| chr17:81436179 | C | T | 5 | a0002c0003t0010g0211 a0002c0021t0002g0088 a0002c0021t0002g0114 others(2): Show |
5 | HG00099.hp2 HG00733.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-2191C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436179 | |||||||
| chr17:81436237 | T | C | 39 | a0001c0001t0001g0109 a0001c0001t0001g0274 a0001c0001t0001g0276 others(36): Show |
40 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.359-2133T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436237 | |||||||
| chr17:81436262 | G | A | 1 | a0004c0004t0002g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.359-2108G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436262 | |||||||
| chr17:81436332 | C | T | 1 | a0044c0081t0001g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.359-2038C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436332 | |||||||
| chr17:81436345 | C | T | 1 | a0002c0003t0003g0293 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.359-2025C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436345 | |||||||
| chr17:81436378 | G | C | 120 | a0001c0001t0001g0109 a0001c0001t0001g0131 a0001c0001t0001g0244 others(117): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.359-1992G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436378 | |||||||
| chr17:81436379 | C | A | 1 | a0009c0072t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.359-1991C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436379 | |||||||
| chr17:81436410 | C | G | 3 | a0007c0007t0001g0005 a0007c0007t0001g0021 a0010c0014t0001g0001 |
4 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-1960C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436410 | |||||||
| chr17:81436416 | G | A | 3 | a0007c0007t0001g0005 a0007c0007t0001g0021 a0010c0014t0001g0001 |
4 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-1954G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436416 | |||||||
| chr17:81436437 | T | C | 1 | a0002c0092t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.359-1933T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436437 | |||||||
| chr17:81436497 | G | A | 2 | a0001c0001t0001g0321 a0001c0075t0001g0303 |
2 | NA18962.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.359-1873G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436497 | |||||||
| chr17:81436596 | G | A | 1 | a0002c0093t0009g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.359-1774G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436596 | |||||||
| chr17:81436617 | G | A | 2 | a0008c0013t0006g0029 a0008c0013t0006g0140 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.359-1753G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436617 | |||||||
| chr17:81436638 | A | C | 35 | a0001c0001t0001g0131 a0001c0001t0001g0244 a0001c0001t0001g0285 others(32): Show |
35 | HG00673.hp1 HG01109.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.359-1732A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436638 | |||||||
| chr17:81436707 | G | A | 1 | a0003c0002t0004g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.359-1663G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436707 | |||||||
| chr17:81436733 | G | A | 17 | a0001c0001t0001g0109 a0002c0009t0001g0034 a0002c0010t0033g0135 others(14): Show |
18 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.359-1637G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436733 | |||||||
| chr17:81436896 | A | T | 1 | a0025c0066t0001g0305 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.359-1474A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436896 | |||||||
| chr17:81436906 | C | T | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.359-1464C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436906 | |||||||
| chr17:81436920 | A | G | 35 | a0001c0001t0001g0131 a0001c0001t0001g0244 a0001c0001t0001g0285 others(32): Show |
35 | HG00673.hp1 HG01109.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.359-1450A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436920 | |||||||
| chr17:81436958 | G | A | 1 | a0004c0004t0002g0240 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.359-1412G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81436958 | |||||||
| chr17:81437074 | G | A | 1 | a0004c0004t0002g0127 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.359-1296G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437074 | |||||||
| chr17:81437156 | C | T | 1 | a0002c0003t0003g0050 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.359-1214C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437156 | |||||||
| chr17:81437433 | G | C | 1 | a0012c0031t0004g0016 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.359-937G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437433 | |||||||
| chr17:81437436 | T | C | 1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.359-934T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437436 | |||||||
| chr17:81437513 | C | T | 1 | a0003c0002t0013g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.359-857C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437513 | |||||||
| chr17:81437660 | C | T | 1 | a0003c0002t0035g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.359-710C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437660 | |||||||
| chr17:81437731 | G | A | 1 | a0031c0098t0002g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359-639G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437731 | |||||||
| chr17:81437819 | C | T | 1 | a0002c0003t0003g0302 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.359-551C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437819 | |||||||
| chr17:81437960 | G | C | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.359-410G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81437960 | |||||||
| chr17:81438085 | G | A | 1 | a0031c0098t0002g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359-285G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81438085 | |||||||
| chr17:81438192 | T | G | 1 | a0004c0011t0002g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.359-178T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81438192 | |||||||
| chr17:81438328 | G | A | 1 | a0002c0021t0002g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.359-42G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 3/27 | chr17 | 81438328 | |||||||
| chr17:81438511 | C | T | 8 | a0004c0004t0002g0003 a0004c0004t0002g0266 a0004c0004t0002g0269 others(5): Show |
9 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.481+19C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438511 | |||||||
| chr17:81438658 | G | T | 10 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0002c0008t0004g0117 others(7): Show |
10 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+166G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438658 | |||||||
| chr17:81438683 | A | G | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.481+191A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438683 | |||||||
| chr17:81438692 | C | T | 21 | a0002c0008t0037g0319 a0003c0018t0002g0144 a0004c0004t0002g0003 others(18): Show |
22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.481+200C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438692 | |||||||
| chr17:81438730 | CTCACTGC others(39): Show |
C | 1 | a0001c0001t0001g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.481+239_481+284del others(46): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438730 | |||||||
| chr17:81438793 | G | A | 2 | a0002c0008t0024g0248 a0002c0008t0025g0253 |
2 | HG01261.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.481+301G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438793 | |||||||
| chr17:81438905 | A | G | 2 | a0019c0030t0007g0032 a0019c0030t0007g0239 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.481+413A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81438905 | |||||||
| chr17:81439016 | C | T | 11 | a0001c0001t0002g0012 a0001c0001t0002g0130 a0002c0008t0004g0117 others(8): Show |
11 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.481+524C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439016 | |||||||
| chr17:81439122 | C | A | 31 | a0002c0008t0037g0319 a0002c0010t0009g0260 a0002c0010t0016g0234 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.481+630C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439122 | |||||||
| chr17:81439205 | A | T | 1 | a0002c0003t0003g0289 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.481+713A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439205 | |||||||
| chr17:81439411 | G | A | 9 | a0002c0003t0010g0211 a0002c0021t0002g0088 a0002c0021t0002g0114 others(6): Show |
9 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.481+919G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439411 | |||||||
| chr17:81439431 | G | C | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.481+939G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439431 | |||||||
| chr17:81439507 | G | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0224 a0001c0001t0001g0287 others(6): Show |
9 | HG00639.hp2 HG01175.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+1015G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439507 | |||||||
| chr17:81439530 | G | A | 49 | a0001c0001t0001g0131 a0001c0001t0001g0244 a0001c0001t0001g0285 others(46): Show |
49 | HG00673.hp1 HG00735.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.481+1038G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439530 | |||||||
| chr17:81439586 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0055c0060t0003g0189 |
3 | NA18747.hp1 NA18986.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.481+1094G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439586 | |||||||
| chr17:81439665 | C | G | 2 | a0002c0025t0003g0065 a0002c0025t0003g0212 |
2 | HG02015.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.481+1173C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439665 | |||||||
| chr17:81439674 | C | T | 1 | a0003c0018t0001g0307 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.481+1182C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439674 | |||||||
| chr17:81439757 | G | A | 107 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(104): Show |
109 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.481+1265G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439757 | |||||||
| chr17:81439812 | T | C | 16 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0324 others(13): Show |
16 | HG01074.hp2 HG02451.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.481+1320T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439812 | |||||||
| chr17:81439831 | C | A | 1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.481+1339C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439831 | |||||||
| chr17:81439943 | G | GGCCTGCA others(7): Show |
2 | a0002c0010t0009g0014 a0002c0010t0016g0161 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.481+1459_481+1472d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81439943 | ||||||
| chr17:81439956 | T | A | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.481+1464T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439956 | |||||||
| chr17:81439956 | T | G | 110 | a0001c0001t0001g0109 a0001c0001t0001g0131 a0001c0001t0001g0244 others(107): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.481+1464T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439956 | |||||||
| chr17:81439971 | C | T | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.481+1479C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81439971 | |||||||
| chr17:81440010 | T | A | 131 | a0001c0001t0001g0109 a0001c0001t0001g0131 a0001c0001t0001g0244 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.481+1518T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440010 | |||||||
| chr17:81440136 | G | A | 1 | a0023c0078t0003g0192 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.481+1644G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440136 | |||||||
| chr17:81440713 | C | T | 8 | a0002c0012t0002g0112 a0005c0005t0005g0202 a0005c0005t0012g0204 others(5): Show |
8 | HG02083.hp2 HG03239.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-1118C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440713 | |||||||
| chr17:81440726 | T | C | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.482-1105T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440726 | |||||||
| chr17:81440751 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0187 |
2 | NA18947.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.482-1080A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440751 | |||||||
| chr17:81440948 | C | A | 1 | a0002c0008t0030g0264 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.482-883C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81440948 | |||||||
| chr17:81441066 | G | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(300): Show |
307 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.482-765G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441066 | |||||||
| chr17:81441199 | G | A | 17 | a0002c0009t0009g0185 a0002c0010t0016g0234 a0002c0068t0007g0254 others(14): Show |
17 | HG00140.hp2 HG01928.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.482-632G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441199 | |||||||
| chr17:81441227 | C | T | 24 | a0002c0010t0016g0234 a0003c0002t0004g0295 a0004c0004t0002g0003 others(21): Show |
25 | HG00140.hp2 HG01243.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.482-604C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441227 | |||||||
| chr17:81441233 | G | A | 1 | a0015c0015t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.482-598G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441233 | |||||||
| chr17:81441269 | C | T | 1 | a0009c0029t0021g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.482-562C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441269 | |||||||
| chr17:81441434 | G | A | 3 | a0005c0005t0012g0204 a0005c0005t0012g0206 a0005c0005t0012g0207 |
3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.482-397G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441434 | |||||||
| chr17:81441438 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.482-393G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441438 | |||||||
| chr17:81441445 | G | A | 1 | a0002c0003t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.482-386G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441445 | |||||||
| chr17:81441458 | C | T | 11 | a0002c0003t0010g0211 a0002c0010t0009g0014 a0002c0010t0033g0135 others(8): Show |
11 | HG00099.hp2 HG00733.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.482-373C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441458 | |||||||
| chr17:81441487 | C | T | 4 | a0002c0003t0003g0110 a0002c0003t0003g0259 a0002c0050t0001g0288 others(1): Show |
4 | HG02074.hp2 HG02083.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-344C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441487 | |||||||
| chr17:81441536 | C | T | 2 | a0005c0005t0008g0296 a0005c0005t0008g0297 |
2 | HG01069.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.482-295C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441536 | |||||||
| chr17:81441655 | C | T | 14 | a0002c0091t0004g0227 a0005c0005t0005g0202 a0005c0005t0008g0085 others(11): Show |
14 | HG00438.hp2 HG01069.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.482-176C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441655 | |||||||
| chr17:81441668 | C | CA | 76 | a0001c0001t0001g0030 a0001c0001t0001g0054 a0001c0001t0001g0075 others(73): Show |
76 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.482-141dupA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81441668 | ||||||
| chr17:81441668 | C | CAA | 6 | a0001c0001t0001g0278 a0002c0008t0006g0134 a0002c0009t0001g0255 others(3): Show |
6 | HG01261.hp1 HG01978.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-142_482-141dup others(2): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81441668 | ||||||
| chr17:81441668 | CA | C | 123 | a0002c0010t0009g0260 a0002c0010t0016g0234 a0002c0025t0003g0065 others(120): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.482-141delA | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81441668 | ||||||
| chr17:81441668 | CAA | C | 6 | a0003c0002t0001g0213 a0004c0004t0002g0003 a0004c0004t0002g0269 others(3): Show |
7 | HG01243.hp1 HG01891.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-142_482-141del others(2): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81441668 | ||||||
| chr17:81441681 | AAAAAAAA others(3): Show |
A | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.482-148_482-139del others(10): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr17 | 81441681 | ||||||
| chr17:81441753 | T | A | 1 | a0011c0017t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.482-78T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 4/27 | chr17 | 81441753 | |||||||
| chr17:81443602 | A | T | 2 | a0019c0030t0007g0032 a0019c0030t0007g0239 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2215+38A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/27 | chr17 | 81443602 | |||||||
| chr17:81443785 | G | A | 11 | a0002c0092t0001g0146 a0006c0006t0001g0009 a0006c0006t0001g0150 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.2216-24G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 5/27 | chr17 | 81443785 | |||||||
| chr17:81444019 | A | G | 1 | a0005c0005t0005g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2324+102A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/27 | chr17 | 81444019 | |||||||
| chr17:81444034 | C | G | 1 | a0051c0100t0001g0237 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2324+117C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/27 | chr17 | 81444034 | |||||||
| chr17:81444086 | G | A | 11 | a0002c0091t0004g0227 a0005c0005t0005g0202 a0005c0005t0008g0085 others(8): Show |
11 | HG00438.hp2 HG01069.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.2324+169G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/27 | chr17 | 81444086 | |||||||
| chr17:81444217 | C | T | 77 | a0002c0010t0009g0014 a0002c0010t0033g0135 a0002c0021t0002g0088 others(74): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.2325-164C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/27 | chr17 | 81444217 | |||||||
| chr17:81444324 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2325-57T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 6/27 | chr17 | 81444324 | |||||||
| chr17:81444636 | G | A | 42 | a0003c0018t0002g0144 a0004c0004t0002g0003 a0004c0004t0002g0010 others(39): Show |
43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.2513-32G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 7/27 | chr17 | 81444636 | |||||||
| chr17:81444907 | T | G | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2671+81T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 8/27 | chr17 | 81444907 | |||||||
| chr17:81444942 | A | G | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2672-73A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 8/27 | chr17 | 81444942 | |||||||
| chr17:81445184 | G | A | 1 | a0019c0030t0007g0032 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.2835+6G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 9/27 | chr17 | 81445184 | |||||||
| chr17:81445721 | C | G | 1 | a0002c0003t0003g0080 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3163+40C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445721 | |||||||
| chr17:81445767 | T | A | 1 | a0001c0056t0003g0284 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3163+86T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445767 | |||||||
| chr17:81445859 | T | A | 87 | a0002c0010t0015g0275 a0002c0084t0001g0070 a0003c0002t0001g0002 others(84): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.3163+178T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445859 | |||||||
| chr17:81445917 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3163+236G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445917 | |||||||
| chr17:81445935 | C | T | 2 | a0002c0010t0016g0161 a0002c0103t0026g0245 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3163+254C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445935 | |||||||
| chr17:81445946 | G | A | 1 | a0009c0029t0021g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3163+265G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445946 | |||||||
| chr17:81445968 | G | A | 1 | a0004c0004t0002g0010 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3163+287G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81445968 | |||||||
| chr17:81446031 | T | A | 9 | a0002c0008t0006g0134 a0002c0008t0030g0264 a0002c0008t0037g0319 others(6): Show |
9 | HG01261.hp1 HG01515.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.3163+350T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446031 | |||||||
| chr17:81446039 | A | G | 5 | a0002c0008t0006g0134 a0008c0013t0006g0029 a0008c0013t0006g0140 others(2): Show |
5 | HG01261.hp1 HG01515.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.3163+358A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446039 | |||||||
| chr17:81446086 | C | A | 86 | a0002c0084t0001g0070 a0003c0002t0001g0002 a0003c0002t0001g0039 others(83): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.3163+405C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446086 | |||||||
| chr17:81446096 | G | C | 4 | a0002c0021t0002g0088 a0002c0021t0002g0114 a0008c0013t0006g0072 others(1): Show |
4 | HG00099.hp2 HG00733.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.3163+415G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446096 | |||||||
| chr17:81446128 | C | T | 1 | a0002c0019t0003g0294 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3163+447C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446128 | |||||||
| chr17:81446144 | A | G | 67 | a0001c0001t0001g0157 a0001c0001t0001g0279 a0001c0001t0002g0177 others(64): Show |
67 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.3163+463A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446144 | |||||||
| chr17:81446253 | G | A | 1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3163+572G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446253 | |||||||
| chr17:81446283 | T | A | 1 | a0009c0072t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3163+602T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446283 | |||||||
| chr17:81446410 | T | C | 220 | a0001c0001t0002g0177 a0001c0001t0007g0090 a0001c0001t0007g0145 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.3164-626T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446410 | |||||||
| chr17:81446449 | C | A | 218 | a0001c0001t0002g0177 a0001c0001t0007g0090 a0001c0001t0007g0145 others(215): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.3164-587C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446449 | |||||||
| chr17:81446464 | T | C | 1 | a0002c0093t0009g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3164-572T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446464 | |||||||
| chr17:81446467 | G | A | 2 | a0002c0010t0016g0161 a0002c0103t0026g0245 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3164-569G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446467 | |||||||
| chr17:81446526 | C | CT | 75 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0075 others(72): Show |
78 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.3164-472dupT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | C | CTT | 48 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0136 others(45): Show |
49 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.3164-473_3164-472d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | C | CTTT | 15 | a0001c0001t0001g0030 a0001c0001t0005g0064 a0001c0016t0001g0181 others(12): Show |
15 | HG00733.hp2 HG01074.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3164-474_3164-472d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | C | CTTTTTTT others(9): Show |
1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3164-487_3164-472d others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | CT | C | 14 | a0001c0075t0001g0303 a0002c0012t0002g0058 a0002c0012t0002g0112 others(11): Show |
14 | HG01069.hp1 HG01123.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.3164-472delT | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | CTTTTTTT others(4): Show |
C | 1 | a0002c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3164-482_3164-472d others(13): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | CTTTTTTT others(6): Show |
C | 1 | a0003c0002t0035g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3164-484_3164-472d others(15): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | CTTTTTTT others(7): Show |
C | 5 | a0002c0003t0003g0184 a0002c0003t0003g0230 a0002c0003t0003g0259 others(2): Show |
5 | HG01516.hp2 NA18950.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.3164-485_3164-472d others(16): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | CTTTTTTT others(8): Show |
C | 57 | a0001c0001t0002g0177 a0001c0001t0007g0090 a0001c0001t0007g0145 others(54): Show |
57 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.3164-486_3164-472d others(17): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | CTTTTTTT others(9): Show |
C | 5 | a0002c0003t0003g0068 a0002c0003t0003g0290 a0002c0003t0010g0211 others(2): Show |
5 | HG00323.hp1 HG01070.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.3164-487_3164-472d others(18): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | CTTTTTTT others(10): Show |
C | 1 | a0002c0008t0030g0264 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3164-488_3164-472d others(19): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | CTTTTTTT others(11): Show |
C | 31 | a0002c0008t0006g0134 a0002c0008t0024g0248 a0002c0008t0025g0253 others(28): Show |
31 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.3164-489_3164-472d others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446526 | CTTTTTTT others(16): Show |
C | 1 | a0002c0008t0004g0117 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3164-494_3164-472d others(25): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr17 | 81446526 | ||||||
| chr17:81446655 | C | T | 2 | a0028c0044t0001g0249 a0036c0045t0004g0273 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3164-381C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446655 | |||||||
| chr17:81446699 | C | T | 2 | a0002c0010t0016g0161 a0002c0103t0026g0245 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3164-337C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446699 | |||||||
| chr17:81446898 | T | C | 43 | a0002c0084t0001g0070 a0003c0002t0001g0002 a0003c0002t0001g0039 others(40): Show |
44 | HG00423.hp2 HG00544.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.3164-138T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446898 | |||||||
| chr17:81446928 | C | T | 24 | a0002c0008t0006g0134 a0002c0021t0002g0088 a0002c0021t0002g0114 others(21): Show |
25 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.3164-108C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446928 | |||||||
| chr17:81446933 | G | A | 1 | a0009c0024t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3164-103G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446933 | |||||||
| chr17:81446995 | A | G | 2 | a0002c0010t0016g0161 a0002c0103t0026g0245 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3164-41A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 10/27 | chr17 | 81446995 | |||||||
| chr17:81447870 | A | AC | 7 | a0001c0001t0002g0084 a0002c0003t0003g0208 a0002c0003t0003g0286 others(4): Show |
7 | HG01496.hp2 HG02300.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3976+28dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr17 | 81447870 | ||||||
| chr17:81447871 | C | A | 90 | a0002c0084t0001g0070 a0003c0002t0001g0002 a0003c0002t0001g0039 others(87): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.3976+23C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81447871 | |||||||
| chr17:81447888 | A | G | 218 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(215): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.3976+40A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81447888 | |||||||
| chr17:81447902 | G | A | 1 | a0014c0022t0011g0322 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3976+54G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81447902 | |||||||
| chr17:81447928 | C | T | 6 | a0007c0007t0001g0005 a0007c0007t0001g0021 a0007c0007t0001g0257 others(3): Show |
6 | HG01243.hp2 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3976+80C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81447928 | |||||||
| chr17:81448119 | C | T | 1 | a0003c0002t0001g0111 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3976+271C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448119 | |||||||
| chr17:81448157 | G | A | 1 | a0003c0002t0001g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3976+309G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448157 | |||||||
| chr17:81448201 | T | A | 2 | a0002c0010t0009g0014 a0002c0093t0009g0015 |
2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3976+353T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448201 | |||||||
| chr17:81448229 | C | T | 1 | a0002c0010t0033g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3976+381C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448229 | |||||||
| chr17:81448296 | G | A | 2 | a0014c0022t0011g0322 a0014c0022t0011g0323 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3976+448G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448296 | |||||||
| chr17:81448324 | A | G | 1 | a0002c0025t0003g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3976+476A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448324 | |||||||
| chr17:81448360 | C | T | 173 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(170): Show |
175 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.3976+512C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448360 | |||||||
| chr17:81448369 | C | T | 2 | a0002c0008t0030g0264 a0002c0008t0037g0319 |
2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3976+521C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448369 | |||||||
| chr17:81448388 | C | T | 5 | a0012c0031t0004g0016 a0012c0031t0004g0018 a0012c0102t0004g0017 others(2): Show |
5 | HG02258.hp2 HG02895.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3976+540C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448388 | |||||||
| chr17:81448431 | G | A | 1 | a0003c0002t0001g0103 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3976+583G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448431 | |||||||
| chr17:81448557 | G | T | 1 | a0001c0001t0002g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3976+709G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448557 | |||||||
| chr17:81448569 | C | T | 1 | a0003c0002t0004g0194 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3976+721C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448569 | |||||||
| chr17:81448582 | G | A | 3 | a0001c0062t0020g0252 a0018c0105t0001g0250 a0056c0104t0010g0160 |
3 | HG02809.hp1 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3976+734G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448582 | |||||||
| chr17:81448599 | G | A | 1 | a0001c0056t0003g0284 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3976+751G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448599 | |||||||
| chr17:81448599 | G | T | 1 | a0004c0004t0029g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3976+751G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448599 | |||||||
| chr17:81448626 | G | A | 27 | a0002c0008t0006g0134 a0002c0010t0009g0014 a0002c0021t0002g0088 others(24): Show |
27 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.3976+778G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448626 | |||||||
| chr17:81448740 | G | A | 89 | a0002c0084t0001g0070 a0003c0002t0001g0002 a0003c0002t0001g0039 others(86): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.3976+892G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448740 | |||||||
| chr17:81448838 | G | A | 1 | a0002c0010t0033g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3976+990G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448838 | |||||||
| chr17:81448874 | A | AC | 27 | a0002c0008t0006g0134 a0002c0010t0009g0014 a0002c0021t0002g0088 others(24): Show |
27 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.3976+1032dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr17 | 81448874 | ||||||
| chr17:81448947 | C | G | 91 | a0002c0084t0001g0070 a0003c0002t0001g0002 a0003c0002t0001g0039 others(88): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.3976+1099C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448947 | |||||||
| chr17:81448978 | G | A | 1 | a0002c0003t0003g0047 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3976+1130G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81448978 | |||||||
| chr17:81449055 | C | T | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3976+1207C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449055 | |||||||
| chr17:81449089 | G | C | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3976+1241G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449089 | |||||||
| chr17:81449101 | G | A | 1 | a0002c0009t0004g0121 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3976+1253G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449101 | |||||||
| chr17:81449177 | C | T | 2 | a0002c0008t0030g0264 a0002c0008t0037g0319 |
2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3976+1329C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449177 | |||||||
| chr17:81449187 | C | T | 11 | a0006c0006t0001g0009 a0006c0006t0001g0150 a0006c0006t0001g0151 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.3976+1339C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449187 | |||||||
| chr17:81449207 | A | G | 56 | a0002c0008t0006g0134 a0002c0008t0024g0248 a0002c0008t0025g0253 others(53): Show |
56 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.3976+1359A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449207 | |||||||
| chr17:81449263 | C | T | 9 | a0004c0004t0002g0003 a0004c0004t0002g0266 a0004c0004t0002g0269 others(6): Show |
10 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.3976+1415C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449263 | |||||||
| chr17:81449316 | G | A | 1 | a0001c0073t0001g0055 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3976+1468G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449316 | |||||||
| chr17:81449428 | A | G | 220 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.3976+1580A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449428 | |||||||
| chr17:81449630 | T | C | 91 | a0002c0084t0001g0070 a0003c0002t0001g0002 a0003c0002t0001g0039 others(88): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.3976+1782T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449630 | |||||||
| chr17:81449646 | C | T | 2 | a0028c0044t0001g0249 a0036c0045t0004g0273 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3976+1798C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449646 | |||||||
| chr17:81449681 | C | G | 1 | a0003c0018t0002g0144 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3976+1833C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449681 | |||||||
| chr17:81449686 | G | A | 2 | a0002c0008t0030g0264 a0002c0008t0037g0319 |
2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3976+1838G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449686 | |||||||
| chr17:81449805 | C | T | 1 | a0045c0057t0017g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3977-1863C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449805 | |||||||
| chr17:81449817 | G | A | 1 | a0003c0063t0005g0198 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3977-1851G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449817 | |||||||
| chr17:81449990 | G | A | 1 | a0002c0008t0030g0264 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3977-1678G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81449990 | |||||||
| chr17:81450069 | G | A | 1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3977-1599G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450069 | |||||||
| chr17:81450282 | G | A | 10 | a0002c0008t0004g0117 a0002c0012t0002g0058 a0002c0012t0002g0112 others(7): Show |
10 | HG01123.hp1 HG01255.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.3977-1386G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450282 | |||||||
| chr17:81450374 | G | A | 61 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(58): Show |
61 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.3977-1294G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450374 | |||||||
| chr17:81450378 | C | A | 11 | a0006c0006t0001g0009 a0006c0006t0001g0150 a0006c0006t0001g0151 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.3977-1290C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450378 | |||||||
| chr17:81450387 | C | T | 5 | a0008c0013t0006g0029 a0008c0013t0006g0140 a0013c0027t0001g0024 others(2): Show |
5 | HG02559.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3977-1281C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450387 | |||||||
| chr17:81450406 | A | C | 1 | a0002c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3977-1262A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450406 | |||||||
| chr17:81450457 | G | A | 1 | a0019c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3977-1211G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450457 | |||||||
| chr17:81450502 | T | C | 219 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(216): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.3977-1166T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450502 | |||||||
| chr17:81450502 | T | G | 1 | a0002c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3977-1166T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450502 | |||||||
| chr17:81450503 | G | T | 1 | a0002c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3977-1165G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450503 | |||||||
| chr17:81450504 | T | C | 1 | a0002c0003t0003g0258 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3977-1164T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450504 | |||||||
| chr17:81450607 | G | A | 1 | a0004c0011t0002g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3977-1061G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450607 | |||||||
| chr17:81450755 | C | T | 3 | a0012c0031t0004g0016 a0012c0031t0004g0018 a0012c0102t0004g0017 |
3 | HG02258.hp2 HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3977-913C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450755 | |||||||
| chr17:81450923 | G | A | 17 | a0002c0003t0003g0050 a0002c0003t0003g0110 a0002c0003t0003g0258 others(14): Show |
17 | HG01433.hp2 HG01943.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.3977-745G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450923 | |||||||
| chr17:81450960 | C | A | 1 | a0003c0002t0035g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3977-708C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81450960 | |||||||
| chr17:81451158 | C | T | 1 | a0019c0030t0007g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3977-510C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451158 | |||||||
| chr17:81451230 | G | A | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0054t0005g0283 |
3 | HG02027.hp1 HG02071.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3977-438G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451230 | |||||||
| chr17:81451234 | A | G | 220 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.3977-434A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451234 | |||||||
| chr17:81451311 | C | T | 7 | a0003c0002t0004g0170 a0003c0002t0004g0171 a0003c0002t0004g0172 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.3977-357C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451311 | |||||||
| chr17:81451400 | C | T | 2 | a0009c0024t0001g0175 a0009c0024t0001g0306 |
2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3977-268C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451400 | |||||||
| chr17:81451573 | C | T | 91 | a0002c0084t0001g0070 a0003c0002t0001g0002 a0003c0002t0001g0039 others(88): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.3977-95C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 11/27 | chr17 | 81451573 | |||||||
| chr17:81451899 | C | T | 4 | a0002c0010t0016g0234 a0002c0010t0033g0135 a0028c0044t0001g0249 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4179+29C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 12/27 | chr17 | 81451899 | |||||||
| chr17:81451957 | G | GC | 81 | a0001c0001t0001g0033 a0002c0003t0003g0044 a0002c0003t0003g0046 others(78): Show |
81 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(78): Show |
splice_region_variant&intron_variant | LOW | c.4180-6dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr17 | 81451957 | ||||||
| chr17:81452132 | C | G | 42 | a0002c0008t0006g0134 a0002c0008t0024g0248 a0002c0008t0025g0253 others(39): Show |
42 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.4316+25C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452132 | |||||||
| chr17:81452133 | TGGGAGGG others(19): Show |
T | 97 | a0002c0010t0015g0275 a0002c0010t0016g0234 a0002c0010t0033g0135 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.4316+33_4316+58del others(26): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr17 | 81452133 | ||||||
| chr17:81452292 | C | A | 6 | a0002c0008t0024g0248 a0002c0008t0025g0253 a0002c0008t0030g0264 others(3): Show |
6 | HG01261.hp2 HG02055.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.4316+185C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452292 | |||||||
| chr17:81452292 | C | T | 1 | a0003c0063t0005g0198 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.4316+185C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452292 | |||||||
| chr17:81452392 | G | A | 62 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(59): Show |
62 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.4316+285G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452392 | |||||||
| chr17:81452668 | T | G | 1 | a0004c0004t0002g0010 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4317-55T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452668 | |||||||
| chr17:81452711 | T | C | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4317-12T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 13/27 | chr17 | 81452711 | |||||||
| chr17:81452929 | T | C | 1 | a0046c0052t0001g0195 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4445+78T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81452929 | |||||||
| chr17:81452969 | A | C | 11 | a0006c0006t0001g0009 a0006c0006t0001g0150 a0006c0006t0001g0151 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.4445+118A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81452969 | |||||||
| chr17:81453158 | C | A | 1 | a0017c0023t0038g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4445+307C>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453158 | |||||||
| chr17:81453198 | C | G | 91 | a0002c0008t0004g0117 a0002c0084t0001g0070 a0003c0002t0001g0002 others(88): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.4445+347C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453198 | |||||||
| chr17:81453253 | C | T | 5 | a0001c0001t0001g0033 a0002c0008t0024g0248 a0002c0008t0025g0253 others(2): Show |
5 | HG01261.hp2 HG02056.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.4445+402C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453253 | |||||||
| chr17:81453411 | G | T | 5 | a0012c0031t0004g0016 a0012c0031t0004g0018 a0012c0102t0004g0017 others(2): Show |
5 | HG02258.hp2 HG02895.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4445+560G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453411 | |||||||
| chr17:81453591 | G | GC | 92 | a0002c0008t0025g0253 a0002c0008t0030g0264 a0002c0008t0037g0319 others(89): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.4445+749dupC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr17 | 81453591 | ||||||
| chr17:81453635 | G | T | 1 | a0040c0046t0027g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4445+784G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453635 | |||||||
| chr17:81453676 | C | T | 2 | a0002c0008t0030g0264 a0002c0008t0037g0319 |
2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4445+825C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453676 | |||||||
| chr17:81453730 | GGCA | G | 11 | a0006c0006t0001g0009 a0006c0006t0001g0150 a0006c0006t0001g0151 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.4445+885_4445+887d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr17 | 81453730 | ||||||
| chr17:81453829 | C | T | 1 | a0004c0037t0014g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4445+978C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453829 | |||||||
| chr17:81453894 | C | T | 1 | a0006c0006t0002g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4445+1043C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453894 | |||||||
| chr17:81453912 | T | C | 1 | a0028c0044t0001g0249 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4445+1061T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453912 | |||||||
| chr17:81453976 | G | A | 18 | a0002c0021t0002g0088 a0002c0021t0002g0114 a0005c0005t0005g0202 others(15): Show |
18 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.4445+1125G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81453976 | |||||||
| chr17:81454091 | G | A | 2 | a0006c0020t0002g0238 a0006c0020t0002g0325 |
2 | HG01074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.4446-1176G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454091 | |||||||
| chr17:81454116 | C | T | 1 | a0009c0029t0021g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4446-1151C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454116 | |||||||
| chr17:81454228 | G | T | 127 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(124): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.4446-1039G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454228 | |||||||
| chr17:81454240 | G | A | 1 | a0006c0006t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.4446-1027G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454240 | |||||||
| chr17:81454446 | G | A | 1 | a0002c0025t0003g0065 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4446-821G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454446 | |||||||
| chr17:81454448 | G | A | 4 | a0002c0010t0016g0234 a0002c0010t0033g0135 a0028c0044t0001g0249 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4446-819G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454448 | |||||||
| chr17:81454508 | CAG | C | 4 | a0002c0008t0024g0248 a0002c0008t0025g0253 a0002c0010t0009g0260 others(1): Show |
4 | HG01261.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4446-758_4446-757d others(4): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454508 | |||||||
| chr17:81454539 | C | CCCCCA | 11 | a0006c0006t0001g0009 a0006c0006t0001g0150 a0006c0006t0001g0151 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.4446-714_4446-710d others(7): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr17 | 81454539 | ||||||
| chr17:81454558 | A | G | 216 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.4446-709A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454558 | |||||||
| chr17:81454573 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4446-694C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454573 | |||||||
| chr17:81454600 | G | A | 2 | a0001c0001t0001g0004 a0018c0036t0001g0019 |
3 | HG02622.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4446-667G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454600 | |||||||
| chr17:81454652 | G | A | 1 | a0002c0003t0003g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4446-615G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454652 | |||||||
| chr17:81454779 | G | A | 1 | a0018c0105t0001g0250 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4446-488G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454779 | |||||||
| chr17:81454868 | G | A | 1 | a0009c0024t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4446-399G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454868 | |||||||
| chr17:81454983 | C | T | 3 | a0014c0022t0011g0322 a0014c0022t0011g0323 a0014c0022t0036g0318 |
3 | HG02647.hp2 HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4446-284C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81454983 | |||||||
| chr17:81455016 | G | A | 4 | a0002c0008t0024g0248 a0002c0008t0025g0253 a0002c0010t0009g0260 others(1): Show |
4 | HG01261.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4446-251G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81455016 | |||||||
| chr17:81455087 | CAGA | C | 4 | a0002c0008t0024g0248 a0002c0008t0025g0253 a0002c0010t0009g0260 others(1): Show |
4 | HG01261.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4446-179_4446-177d others(5): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81455087 | |||||||
| chr17:81455154 | G | C | 1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4446-113G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81455154 | |||||||
| chr17:81455226 | G | A | 90 | a0002c0084t0001g0070 a0003c0002t0001g0002 a0003c0002t0001g0039 others(87): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.4446-41G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81455226 | |||||||
| chr17:81455263 | C | T | 90 | a0002c0084t0001g0070 a0003c0002t0001g0002 a0003c0002t0001g0039 others(87): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
splice_region_variant&intron_variant | LOW | c.4446-4C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 14/27 | chr17 | 81455263 | |||||||
| chr17:81455400 | G | A | 1 | a0002c0010t0009g0260 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4569+10G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455400 | |||||||
| chr17:81455457 | T | G | 2 | a0001c0001t0001g0004 a0018c0036t0001g0019 |
3 | HG02622.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4569+67T>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455457 | |||||||
| chr17:81455529 | C | T | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4569+139C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455529 | |||||||
| chr17:81455530 | G | A | 1 | a0014c0022t0011g0322 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4569+140G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455530 | |||||||
| chr17:81455628 | G | A | 3 | a0005c0005t0008g0296 a0005c0005t0008g0297 a0033c0088t0001g0261 |
3 | HG01069.hp2 HG01934.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.4569+238G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455628 | |||||||
| chr17:81455675 | A | G | 2 | a0028c0044t0001g0249 a0036c0045t0004g0273 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.4569+285A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455675 | |||||||
| chr17:81455779 | G | C | 1 | a0005c0005t0008g0297 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4569+389G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455779 | |||||||
| chr17:81455895 | C | T | 1 | a0017c0023t0015g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4570-402C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455895 | |||||||
| chr17:81455986 | T | C | 1 | a0009c0024t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4570-311T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81455986 | |||||||
| chr17:81456033 | A | C | 3 | a0003c0002t0004g0280 a0003c0002t0004g0295 a0003c0063t0005g0198 |
3 | NA18612.hp1 NA18942.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.4570-264A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81456033 | |||||||
| chr17:81456202 | C | T | 2 | a0002c0008t0030g0264 a0002c0008t0037g0319 |
2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4570-95C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 15/27 | chr17 | 81456202 | |||||||
| chr17:81456623 | C | T | 1 | a0002c0010t0016g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4858+38C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81456623 | |||||||
| chr17:81456716 | G | A | 2 | a0002c0008t0030g0264 a0002c0008t0037g0319 |
2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4858+131G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81456716 | |||||||
| chr17:81456799 | C | T | 5 | a0012c0031t0004g0016 a0012c0031t0004g0018 a0012c0102t0004g0017 others(2): Show |
5 | HG02258.hp2 HG02895.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4858+214C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81456799 | |||||||
| chr17:81456945 | AC | A | 202 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(199): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.4858+368delC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr17 | 81456945 | ||||||
| chr17:81457102 | G | A | 90 | a0002c0084t0001g0070 a0003c0002t0001g0002 a0003c0002t0001g0039 others(87): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.4859-308G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81457102 | |||||||
| chr17:81457221 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4859-189C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81457221 | |||||||
| chr17:81457258 | C | T | 2 | a0010c0014t0001g0001 a0010c0014t0001g0243 |
3 | HG00639.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4859-152C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81457258 | |||||||
| chr17:81457369 | C | G | 1 | a0003c0002t0001g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4859-41C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 16/27 | chr17 | 81457369 | |||||||
| chr17:81457577 | A | AGGCAGGG others(23): Show |
1 | a0039c0087t0004g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5028_5041+16dupGCA others(27): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr17 | 81457577 | ||||||
| chr17:81457605 | G | A | 7 | a0006c0006t0001g0009 a0006c0006t0001g0150 a0006c0006t0001g0151 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.5041+13G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81457605 | |||||||
| chr17:81457904 | AGGGAGGG others(52): Show |
A | 4 | a0003c0002t0001g0049 a0003c0002t0004g0280 a0003c0002t0004g0295 others(1): Show |
4 | NA18612.hp1 NA18942.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.5042-204_5042-146d others(61): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr17 | 81457904 | ||||||
| chr17:81457939 | G | C | 1 | a0006c0020t0002g0325 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5042-226G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81457939 | |||||||
| chr17:81457960 | C | T | 1 | a0016c0106t0010g0328 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5042-205C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81457960 | |||||||
| chr17:81457994 | G | C | 3 | a0011c0017t0001g0228 a0011c0017t0001g0299 a0029c0076t0001g0094 |
3 | HG01106.hp2 HG01975.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.5042-171G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81457994 | |||||||
| chr17:81458066 | G | T | 1 | a0048c0090t0001g0042 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5042-99G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81458066 | |||||||
| chr17:81458115 | C | T | 56 | a0002c0003t0003g0044 a0002c0003t0003g0046 a0002c0003t0003g0047 others(53): Show |
56 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.5042-50C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 17/27 | chr17 | 81458115 | |||||||
| chr17:81458482 | G | A | 1 | a0007c0007t0001g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5343+16G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | chr17 | 81458482 | |||||||
| chr17:81458507 | G | A | 2 | a0002c0010t0016g0161 a0002c0103t0026g0245 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.5343+41G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | chr17 | 81458507 | |||||||
| chr17:81458529 | C | T | 3 | a0005c0005t0012g0204 a0005c0005t0012g0206 a0005c0005t0012g0207 |
3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.5343+63C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | chr17 | 81458529 | |||||||
| chr17:81458532 | C | CCTCCCCC others(3): Show |
93 | a0002c0010t0016g0161 a0002c0010t0016g0234 a0002c0010t0033g0135 others(90): Show |
95 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.5343+68_5343+77dup others(10): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr17 | 81458532 | ||||||
| chr17:81458532 | C | CCTCCCCC others(13): Show |
1 | a0003c0002t0001g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.5343+77_5344-77ins others(20): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr17 | 81458532 | ||||||
| chr17:81458583 | C | T | 10 | a0002c0008t0004g0117 a0002c0012t0002g0058 a0002c0012t0002g0112 others(7): Show |
10 | HG01123.hp1 HG01255.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.5344-38C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | chr17 | 81458583 | |||||||
| chr17:81458614 | C | T | 10 | a0002c0008t0004g0117 a0002c0012t0002g0058 a0002c0012t0002g0112 others(7): Show |
10 | HG01123.hp1 HG01255.hp2 HG01346.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.5344-7C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 18/27 | chr17 | 81458614 | |||||||
| chr17:81458995 | GC | G | 40 | a0003c0018t0002g0144 a0003c0018t0002g0210 a0004c0004t0002g0003 others(37): Show |
41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.5605+28delC | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr17 | 81458995 | ||||||
| chr17:81458997 | C | T | 4 | a0002c0009t0009g0185 a0002c0068t0007g0254 a0002c0101t0010g0020 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.5605+28C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 20/27 | chr17 | 81458997 | |||||||
| chr17:81459029 | G | A | 1 | a0036c0045t0004g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5606-25G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 20/27 | chr17 | 81459029 | |||||||
| chr17:81459235 | A | G | 1 | a0004c0004t0029g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5721-18A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 21/27 | chr17 | 81459235 | |||||||
| chr17:81459340 | G | T | 2 | a0010c0014t0001g0001 a0010c0014t0001g0243 |
3 | HG00639.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.5796+12G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/27 | chr17 | 81459340 | |||||||
| chr17:81459342 | C | T | 1 | a0041c0107t0002g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5796+14C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/27 | chr17 | 81459342 | |||||||
| chr17:81459356 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.5796+28G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/27 | chr17 | 81459356 | |||||||
| chr17:81459390 | A | G | 92 | a0002c0012t0002g0058 a0002c0012t0002g0159 a0003c0002t0001g0002 others(89): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.5796+62A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/27 | chr17 | 81459390 | |||||||
| chr17:81459455 | A | G | 205 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0002c0003t0003g0044 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.5797-41A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 22/27 | chr17 | 81459455 | |||||||
| chr17:81459682 | C | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(115): Show |
120 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.5905+78C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459682 | |||||||
| chr17:81459730 | C | T | 82 | a0003c0002t0001g0002 a0003c0002t0001g0039 a0003c0002t0001g0049 others(79): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.5905+126C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459730 | |||||||
| chr17:81459785 | G | C | 1 | a0002c0010t0015g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5905+181G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459785 | |||||||
| chr17:81459800 | C | T | 1 | a0045c0057t0017g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5905+196C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459800 | |||||||
| chr17:81459913 | C | T | 2 | a0002c0010t0016g0234 a0002c0010t0033g0135 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.5905+309C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459913 | |||||||
| chr17:81459980 | C | T | 2 | a0003c0002t0004g0170 a0003c0002t0004g0171 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.5906-297C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459980 | |||||||
| chr17:81459988 | G | T | 1 | a0010c0014t0001g0001 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.5906-289G>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81459988 | |||||||
| chr17:81460028 | G | C | 34 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0086 others(31): Show |
34 | HG00423.hp1 HG00673.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.5906-249G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81460028 | |||||||
| chr17:81460041 | G | A | 1 | a0009c0024t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5906-236G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81460041 | |||||||
| chr17:81460232 | G | A | 68 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0033 others(65): Show |
68 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.5906-45G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 23/27 | chr17 | 81460232 | |||||||
| chr17:81460481 | G | C | 1 | a0005c0005t0008g0087 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.6026-49G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 24/27 | chr17 | 81460481 | |||||||
| chr17:81460501 | C | G | 1 | a0001c0001t0002g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.6026-29C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 24/27 | chr17 | 81460501 | |||||||
| chr17:81460768 | C | G | 51 | a0001c0056t0003g0284 a0002c0003t0003g0044 a0002c0003t0003g0046 others(48): Show |
51 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.6202+62C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 25/27 | chr17 | 81460768 | |||||||
| chr17:81460796 | C | T | 175 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(172): Show |
178 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.6203-70C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 25/27 | chr17 | 81460796 | |||||||
| chr17:81460823 | G | A | 2 | a0002c0008t0030g0264 a0002c0008t0037g0319 |
2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6203-43G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 25/27 | chr17 | 81460823 | |||||||
| chr17:81460859 | C | G | 1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | splice_region_variant&intron_variant | LOW | c.6203-7C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 25/27 | chr17 | 81460859 | |||||||
| chr17:81462054 | C | T | 2 | a0002c0008t0030g0264 a0002c0008t0037g0319 |
2 | HG02055.hp1 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.7383+8C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462054 | |||||||
| chr17:81462202 | A | G | 149 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(146): Show |
152 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.7383+156A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462202 | |||||||
| chr17:81462204 | G | A | 3 | a0003c0002t0004g0170 a0003c0002t0004g0171 a0003c0002t0004g0172 |
3 | HG01167.hp2 HG01169.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.7383+158G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462204 | |||||||
| chr17:81462221 | G | A | 4 | a0008c0013t0006g0029 a0008c0013t0006g0072 a0008c0013t0006g0140 others(1): Show |
4 | HG01192.hp2 HG01516.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.7383+175G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462221 | |||||||
| chr17:81462227 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.7383+181G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462227 | |||||||
| chr17:81462239 | C | T | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.7383+193C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462239 | |||||||
| chr17:81462292 | T | C | 325 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(322): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.7383+246T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462292 | |||||||
| chr17:81462332 | T | C | 278 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(275): Show |
281 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.7383+286T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462332 | |||||||
| chr17:81462382 | C | G | 25 | a0002c0012t0002g0058 a0002c0012t0002g0112 a0002c0012t0002g0133 others(22): Show |
25 | HG00099.hp2 HG00733.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.7383+336C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462382 | |||||||
| chr17:81462423 | T | C | 3 | a0016c0106t0010g0328 a0017c0023t0015g0277 a0017c0023t0038g0027 |
3 | HG02486.hp1 HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.7384-317T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462423 | |||||||
| chr17:81462462 | T | A | 1 | a0001c0001t0001g0109 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.7384-278T>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462462 | |||||||
| chr17:81462463 | G | C | 2 | a0002c0010t0016g0234 a0002c0010t0033g0135 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.7384-277G>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462463 | |||||||
| chr17:81462502 | A | G | 1 | a0002c0103t0026g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.7384-238A>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462502 | |||||||
| chr17:81462512 | C | T | 1 | a0045c0057t0017g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7384-228C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462512 | |||||||
| chr17:81462549 | C | G | 50 | a0001c0056t0003g0284 a0002c0003t0003g0044 a0002c0003t0003g0046 others(47): Show |
50 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.7384-191C>G | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462549 | |||||||
| chr17:81462576 | G | A | 7 | a0001c0001t0006g0149 a0002c0008t0006g0134 a0008c0013t0006g0029 others(4): Show |
7 | HG01192.hp2 HG01261.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.7384-164G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462576 | |||||||
| chr17:81462597 | G | A | 1 | a0045c0057t0017g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7384-143G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462597 | |||||||
| chr17:81462624 | A | T | 3 | a0002c0021t0002g0088 a0002c0021t0002g0114 a0021c0094t0002g0147 |
3 | HG00099.hp2 HG00733.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.7384-116A>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462624 | |||||||
| chr17:81462685 | C | T | 173 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(170): Show |
176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.7384-55C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 26/27 | chr17 | 81462685 | |||||||
| chr17:81463009 | C | T | 25 | a0002c0012t0002g0058 a0002c0012t0002g0112 a0002c0012t0002g0133 others(22): Show |
25 | HG00099.hp2 HG00733.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.7620+33C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463009 | |||||||
| chr17:81463090 | C | T | 3 | a0003c0002t0001g0049 a0009c0024t0001g0175 a0009c0024t0001g0306 |
3 | HG03831.hp2 HG04204.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.7620+114C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463090 | |||||||
| chr17:81463106 | C | T | 1 | a0007c0007t0004g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7620+130C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463106 | |||||||
| chr17:81463132 | A | C | 4 | a0004c0011t0002g0120 a0004c0011t0002g0163 a0004c0011t0004g0071 others(1): Show |
4 | HG01074.hp1 HG02735.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.7620+156A>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463132 | |||||||
| chr17:81463175 | T | C | 3 | a0003c0018t0002g0210 a0004c0004t0002g0092 a0004c0004t0002g0093 |
3 | HG00733.hp2 HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.7620+199T>C | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463175 | |||||||
| chr17:81463230 | G | A | 1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7620+254G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463230 | |||||||
| chr17:81463359 | C | T | 1 | a0002c0003t0003g0048 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.7621-252C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463359 | |||||||
| chr17:81463369 | G | A | 2 | a0002c0010t0016g0234 a0002c0010t0033g0135 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.7621-242G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463369 | |||||||
| chr17:81463529 | G | A | 1 | a0002c0010t0016g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7621-82G>A | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463529 | |||||||
| chr17:81463530 | G | GTGGGCGG others(15): Show |
1 | a0002c0003t0003g0304 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.7621-75_7621-54dup others(22): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr17 | 81463530 | ||||||
| chr17:81463535 | C | T | 1 | a0002c0003t0003g0047 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.7621-76C>T | BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 27/27 | chr17 | 81463535 |