Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 374860 |
|---|---|
| ensemblid | ENSG00000180777.15 |
| hgncid | 24165 |
| symbol | ANKRD30B |
| name | ankyrin repeat domain 30B |
| refseq_nuc | NM_001367607.2 |
| refseq_prot | NP_001354536.1 |
| ensembl_nuc | ENST00000690538.1 |
| ensembl_prot | ENSP00000510074.1 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 14748172 |
| end | 14854667 |
| strand | + |
| ver | v1.2 |
| region | chr18:14748172-14854667 |
| region5000 | chr18:14743172-14859667 |
| regionname0 | ANKRD30B_chr18_14748172_14854667 |
| regionname5000 | ANKRD30B_chr18_14743172_14859667 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1525 | 143 | 31 | 29 | 60 | 4 | 18 | 46 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0002 | 0/0 | 1525 | 89 | 1 | 19 | 55 | 3 | 11 | 40 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0003 | 0/0 | 1525 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0004 | 0/0 | 1525 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0005 | 0/0 | 1525 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0006 | 0/0 | 1525 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0007 | 0/0 | 1525 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0008 | 0/0 | 1525 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0009 | 0/0 | 1406 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0010 | 0/0 | 896 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0011 | 0/0 | 1525 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0012 | 0/0 | 1525 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0013 | 0/0 | 1525 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0014 | 0/0 | 1525 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0015 | 0/0 | 1406 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0016 | 0/0 | 1525 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0017 | 0/0 | 1525 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0018 | 0/0 | 1525 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0019 | 0/0 | 1525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0020 | 0/0 | 1525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0021 | 0/0 | 1525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0022 | 0/0 | 1525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0023 | 0/0 | 1525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0024 | 0/0 | 1525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0025 | 0/0 | 1406 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0026 | 0/0 | 1525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0027 | 0/0 | 1525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0028 | 0/0 | 1525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0029 | 0/0 | 1525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0030 | 0/0 | 1525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0031 | 0/0 | 1406 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0032 | 1/0 | 1525 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0033 | 0/0 | 1525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0034 | 0/0 | 1525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0035 | 0/0 | 1525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0036 | 0/0 | 1525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0037 | 0/0 | 896 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0038 | 0/0 | 1525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0039 | 0/0 | 1525 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0040 | 0/0 | 1525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0041 | 0/0 | 1525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0042 | 0/0 | 1406 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0043 | 0/0 | 1525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0044 | 0/0 | 1525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0045 | 0/0 | 1525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 4578 | 92 | 17 | 13 | 43 | 3 | 15 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0002 | 0/0 | 4578 | 71 | 1 | 16 | 48 | 2 | 4 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0003 | 0/0 | 4578 | 37 | 12 | 12 | 13 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0004 | 0/0 | 4578 | 18 | 0 | 3 | 7 | 1 | 7 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0005 | 0/0 | 4578 | 6 | 6 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0006 | 0/0 | 4578 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0007 | 0/0 | 4578 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0008 | 0/0 | 4578 | 4 | 3 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0009 | 0/0 | 4578 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0010 | 0/0 | 4578 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0011 | 0/0 | 4578 | 4 | 0 | 3 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0012 | 0/0 | 4578 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0013 | 0/0 | 4221 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0014 | 0/0 | 4578 | 3 | 1 | 0 | 2 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0015 | 0/0 | 4578 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0016 | 0/0 | 4578 | 2 | 1 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0017 | 0/0 | 4578 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0018 | 0/0 | 4578 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0019 | 0/0 | 4578 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0020 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0021 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0022 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0023 | 0/0 | 4221 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0024 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0025 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0026 | 0/0 | 15460 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0027 | 0/0 | 15460 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0028 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0029 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0030 | 0/0 | 4221 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0031 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0032 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0033 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0034 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0035 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0036 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0037 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0038 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0039 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0040 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0041 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0042 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0043 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0044 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0045 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0046 | 1/0 | 4578 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0047 | 0/0 | 4221 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0048 | 0/0 | 4221 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0049 | 0/0 | 15460 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0050 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0051 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0052 | 0/0 | 4221 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0053 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0054 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0055 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0056 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0057 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0058 | 0/0 | 15464 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0059 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0060 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0061 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0062 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0063 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0064 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| c0065 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 758 | 178 | 36 | 40 | 78 | 4 | 19 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0002 | 0/0 | 758 | 67 | 3 | 8 | 41 | 4 | 11 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0003 | 0/1 | 758 | 28 | 5 | 5 | 15 | 0 | 2 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0004 | 0/0 | 758 | 15 | 14 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0005 | 0/0 | 758 | 7 | 7 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0006 | 0/0 | 758 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0007 | 0/0 | 758 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0008 | 0/0 | 758 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0009 | 0/0 | 758 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0010 | 0/0 | 758 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0011 | 0/0 | 758 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0012 | 0/0 | 758 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| t0013 | 0/0 | 758 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4578 | 92 | 17 | 13 | 43 | 3 | 15 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0003 | 0/0 | 4578 | 37 | 12 | 12 | 13 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0011 | 0/0 | 4578 | 4 | 0 | 3 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0015 | 0/0 | 4578 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0036 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0037 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0041 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0055 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0059 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0060 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0063 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0002c0002 | 0/0 | 4578 | 71 | 1 | 16 | 48 | 2 | 4 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0002c0004 | 0/0 | 4578 | 18 | 0 | 3 | 7 | 1 | 7 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0003c0006 | 0/0 | 4578 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0003c0019 | 0/0 | 4578 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0003c0021 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0004c0007 | 0/0 | 4578 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0004c0022 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0004c0045 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0005c0005 | 0/0 | 4578 | 6 | 6 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0006c0008 | 0/0 | 4578 | 4 | 3 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0007c0009 | 0/0 | 4578 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0008c0010 | 0/0 | 4578 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0009c0013 | 0/0 | 4221 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0010c0026 | 0/0 | 15460 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0010c0027 | 0/0 | 15460 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0010c0049 | 0/0 | 15460 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0011c0014 | 0/0 | 4578 | 3 | 1 | 0 | 2 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0012c0012 | 0/0 | 4578 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0013c0017 | 0/0 | 4578 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0014c0018 | 0/0 | 4578 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0015c0023 | 0/0 | 4221 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0015c0048 | 0/0 | 4221 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0016c0031 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0016c0050 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0017c0016 | 0/0 | 4578 | 2 | 1 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0018c0032 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0018c0051 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0019c0020 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0020c0040 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0021c0042 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0022c0061 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0023c0043 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0024c0038 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0025c0030 | 0/0 | 4221 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0026c0029 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0027c0028 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0028c0025 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0029c0024 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0030c0062 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0031c0047 | 0/0 | 4221 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0032c0046 | 1/0 | 4578 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0033c0044 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0034c0053 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0035c0054 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0036c0035 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0037c0058 | 0/0 | 15464 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0038c0057 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0039c0056 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0040c0033 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0041c0034 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0042c0052 | 0/0 | 4221 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0043c0039 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0044c0064 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0045c0065 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5335 | 31 | 9 | 9 | 9 | 0 | 4 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0001t0002 | 0/0 | 5335 | 40 | 0 | 2 | 24 | 3 | 11 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0001t0003 | 0/1 | 5335 | 17 | 5 | 2 | 9 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0001t0004 | 0/0 | 5335 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0001t0011 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0001t0013 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0003t0001 | 0/0 | 5335 | 8 | 0 | 6 | 2 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0003t0002 | 0/0 | 5335 | 18 | 3 | 5 | 10 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0003t0003 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0003t0004 | 0/0 | 5335 | 8 | 7 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0003t0009 | 0/0 | 5335 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0011t0003 | 0/0 | 5335 | 4 | 0 | 3 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0015t0001 | 0/0 | 5335 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0036t0002 | 0/0 | 5335 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0037t0003 | 0/0 | 5335 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0041t0001 | 0/0 | 5335 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0055t0001 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0059t0002 | 0/0 | 5335 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0060t0002 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0001c0063t0004 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0002c0002t0001 | 0/0 | 5335 | 70 | 1 | 16 | 47 | 2 | 4 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0002c0002t0012 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0002c0004t0001 | 0/0 | 5335 | 18 | 0 | 3 | 7 | 1 | 7 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0003c0006t0001 | 0/0 | 5335 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0003c0006t0008 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0003c0019t0001 | 0/0 | 5335 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0003c0021t0001 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0004c0007t0001 | 0/0 | 5335 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0004c0022t0001 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0004c0045t0010 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0005c0005t0001 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0005c0005t0006 | 0/0 | 5335 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0006c0008t0001 | 0/0 | 5335 | 4 | 3 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0007c0009t0007 | 0/0 | 5335 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0008c0010t0001 | 0/0 | 5335 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0008c0010t0008 | 0/0 | 5335 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0009c0013t0005 | 0/0 | 4978 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0010c0026t0001 | 0/0 | 16217 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0010c0027t0001 | 0/0 | 16217 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0010c0049t0001 | 0/0 | 16217 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0011c0014t0001 | 0/0 | 5335 | 3 | 1 | 0 | 2 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0012c0012t0002 | 0/0 | 5335 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0013c0017t0001 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0013c0017t0005 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0014c0018t0005 | 0/0 | 5335 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0015c0023t0001 | 0/0 | 4978 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0015c0048t0001 | 0/0 | 4978 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0016c0031t0003 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0016c0050t0003 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0017c0016t0003 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0017c0016t0004 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0018c0032t0002 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0018c0051t0003 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0019c0020t0001 | 0/0 | 5335 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0020c0040t0001 | 0/0 | 5335 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0021c0042t0005 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0022c0061t0002 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0023c0043t0001 | 0/0 | 5335 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0024c0038t0008 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0025c0030t0001 | 0/0 | 4978 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0026c0029t0001 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0027c0028t0001 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0028c0025t0001 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0029c0024t0001 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0030c0062t0001 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0031c0047t0001 | 0/0 | 4978 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0032c0046t0001 | 1/0 | 5335 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0033c0044t0001 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0034c0053t0010 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0035c0054t0001 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0036c0035t0004 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0037c0058t0002 | 0/0 | 16221 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0038c0057t0003 | 0/0 | 5335 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0039c0056t0001 | 0/0 | 5335 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0040c0033t0004 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0041c0034t0004 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0042c0052t0001 | 0/0 | 4978 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0043c0039t0009 | 0/0 | 5335 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0044c0064t0001 | 0/0 | 5335 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| a0045c0065t0001 | 0/0 | 5335 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | copy fasta | chr18 | 14743172 | 14859667 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0011g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0001t0013g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0003t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0011t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0011t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0011t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0011t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0015t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0015t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0015t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0036t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0037t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0041t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0055t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0059t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0060t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0001c0063t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0002t0012g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0002c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0003c0006t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0003c0006t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0003c0006t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0003c0006t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0003c0019t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0003c0019t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0003c0021t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0004c0007t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0004c0007t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0004c0007t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0004c0007t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0004c0022t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0004c0045t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0005c0005t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0005c0005t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0005c0005t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0005c0005t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0005c0005t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0005c0005t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0006c0008t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0006c0008t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0006c0008t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0006c0008t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0007c0009t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0007c0009t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0007c0009t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0007c0009t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0008c0010t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0008c0010t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0008c0010t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0008c0010t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0009c0013t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0009c0013t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0009c0013t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0010c0026t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0010c0027t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0010c0049t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0011c0014t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0011c0014t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0011c0014t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0012c0012t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0012c0012t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0012c0012t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0013c0017t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0013c0017t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0014c0018t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0014c0018t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0015c0023t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0015c0048t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0016c0031t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0016c0050t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0017c0016t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0017c0016t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0018c0032t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0018c0051t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0019c0020t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0020c0040t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0021c0042t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0022c0061t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0023c0043t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0024c0038t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0025c0030t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0026c0029t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0027c0028t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0028c0025t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0029c0024t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0030c0062t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0031c0047t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0032c0046t0001g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0033c0044t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0034c0053t0010g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0035c0054t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0036c0035t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0037c0058t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0038c0057t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0039c0056t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0040c0033t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0041c0034t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0042c0052t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0043c0039t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0044c0064t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| a0045c0065t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0210 | EUR | GBR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00099 | hp2 | a0001 | c0036 | t0002 | g0192 | EUR | GBR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00323 | hp1 | a0002 | c0004 | t0001 | g0278 | EUR | FIN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | FIN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00544 | hp2 | a0035 | c0054 | t0001 | g0258 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00609 | hp1 | a0016 | c0050 | t0003 | g0059 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00609 | hp2 | a0026 | c0029 | t0001 | g0203 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00621 | hp1 | a0001 | c0001 | t0011 | g0022 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0185 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0186 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00673 | hp2 | a0002 | c0004 | t0001 | g0076 | EAS | CHS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00735 | hp1 | a0001 | c0011 | t0003 | g0280 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0168 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0193 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG00738 | hp2 | a0002 | c0004 | t0001 | g0254 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0127 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0112 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01081 | hp1 | a0045 | c0065 | t0001 | g0194 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01167 | hp2 | a0001 | c0003 | t0004 | g0307 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0123 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0125 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01243 | hp1 | a0023 | c0043 | t0001 | g0095 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01243 | hp2 | a0001 | c0059 | t0002 | g0050 | AMR | PUR | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0279 | AMR | CLM | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | CLM | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0217 | AMR | CLM | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0216 | AMR | CLM | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | CLM | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0126 | AMR | CLM | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01515 | hp1 | a0039 | c0056 | t0001 | g0257 | EUR | IBS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0061 | EUR | IBS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0130 | EUR | IBS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01891 | hp1 | a0030 | c0062 | t0001 | g0094 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01891 | hp2 | a0006 | c0008 | t0001 | g0190 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01928 | hp1 | a0025 | c0030 | t0001 | g0114 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01943 | hp1 | a0002 | c0004 | t0001 | g0029 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01952 | hp1 | a0006 | c0008 | t0001 | g0171 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0113 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01978 | hp2 | a0001 | c0011 | t0003 | g0223 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01993 | hp1 | a0019 | c0020 | t0001 | g0234 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02004 | hp1 | a0002 | c0004 | t0001 | g0021 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02004 | hp2 | a0044 | c0064 | t0001 | g0218 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02027 | hp2 | a0001 | c0003 | t0002 | g0205 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02055 | hp1 | a0029 | c0024 | t0001 | g0235 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02055 | hp2 | a0036 | c0035 | t0004 | g0306 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02056 | hp1 | a0001 | c0003 | t0002 | g0155 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02080 | hp1 | a0001 | c0003 | t0002 | g0224 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0151 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02132 | hp2 | a0002 | c0004 | t0001 | g0014 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02135 | hp2 | a0012 | c0012 | t0002 | g0108 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02145 | hp2 | a0011 | c0014 | t0001 | g0086 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0169 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02165 | hp1 | a0016 | c0031 | t0003 | g0124 | EAS | CDX | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | CDX | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02257 | hp1 | a0001 | c0063 | t0004 | g0297 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02258 | hp1 | a0001 | c0003 | t0004 | g0308 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02258 | hp2 | a0007 | c0009 | t0007 | g0227 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02280 | hp1 | a0001 | c0003 | t0004 | g0305 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02280 | hp2 | a0005 | c0005 | t0006 | g0246 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0120 | AMR | PEL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02451 | hp1 | a0001 | c0003 | t0009 | g0228 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02451 | hp2 | a0004 | c0007 | t0001 | g0310 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | KHV | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02572 | hp2 | a0004 | c0022 | t0001 | g0301 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02615 | hp1 | a0008 | c0010 | t0008 | g0007 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02615 | hp2 | a0017 | c0016 | t0004 | g0294 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02622 | hp1 | a0043 | c0039 | t0009 | g0230 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02622 | hp2 | a0005 | c0005 | t0006 | g0245 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02630 | hp1 | a0001 | c0003 | t0004 | g0295 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02630 | hp2 | a0008 | c0010 | t0001 | g0262 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02647 | hp1 | a0009 | c0013 | t0005 | g0104 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02647 | hp2 | a0001 | c0003 | t0004 | g0298 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02683 | hp2 | a0001 | c0037 | t0003 | g0191 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0212 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02698 | hp2 | a0002 | c0004 | t0001 | g0288 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02717 | hp1 | a0008 | c0010 | t0001 | g0261 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02717 | hp2 | a0008 | c0010 | t0008 | g0006 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02723 | hp1 | a0003 | c0019 | t0001 | g0091 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02723 | hp2 | a0005 | c0005 | t0001 | g0302 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02735 | hp2 | a0002 | c0004 | t0001 | g0070 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02738 | hp1 | a0010 | c0026 | t0001 | g0121 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02738 | hp2 | a0001 | c0041 | t0001 | g0249 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02809 | hp1 | a0003 | c0021 | t0001 | g0239 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02818 | hp1 | a0034 | c0053 | t0010 | g0093 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02818 | hp2 | a0014 | c0018 | t0005 | g0103 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02886 | hp1 | a0003 | c0006 | t0001 | g0237 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02895 | hp2 | a0004 | c0007 | t0001 | g0005 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02896 | hp1 | a0003 | c0006 | t0001 | g0240 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02897 | hp2 | a0004 | c0007 | t0001 | g0005 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02922 | hp1 | a0006 | c0008 | t0001 | g0163 | AFR | ESN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02922 | hp2 | a0005 | c0005 | t0006 | g0233 | AFR | ESN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02965 | hp2 | a0003 | c0019 | t0001 | g0090 | AFR | ESN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03041 | hp2 | a0001 | c0003 | t0004 | g0244 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03098 | hp1 | a0009 | c0013 | t0005 | g0105 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03130 | hp1 | a0004 | c0007 | t0001 | g0309 | AFR | ESN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03130 | hp2 | a0024 | c0038 | t0008 | g0238 | AFR | ESN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03139 | hp1 | a0031 | c0047 | t0001 | g0255 | AFR | ESN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03139 | hp2 | a0007 | c0009 | t0007 | g0226 | AFR | ESN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03195 | hp1 | a0005 | c0005 | t0006 | g0232 | AFR | ESN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03195 | hp2 | a0007 | c0009 | t0007 | g0128 | AFR | ESN | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03209 | hp1 | a0003 | c0006 | t0001 | g0003 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03209 | hp2 | a0001 | c0055 | t0001 | g0088 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03225 | hp1 | a0001 | c0003 | t0009 | g0229 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03225 | hp2 | a0003 | c0006 | t0001 | g0003 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03453 | hp1 | a0001 | c0003 | t0002 | g0106 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03453 | hp2 | a0013 | c0017 | t0001 | g0009 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03486 | hp1 | a0040 | c0033 | t0004 | g0304 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03486 | hp2 | a0004 | c0045 | t0010 | g0089 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03491 | hp1 | a0002 | c0004 | t0001 | g0004 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03492 | hp1 | a0001 | c0011 | t0003 | g0270 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03492 | hp2 | a0002 | c0004 | t0001 | g0004 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03540 | hp1 | a0001 | c0003 | t0004 | g0303 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03540 | hp2 | a0014 | c0018 | t0005 | g0102 | AFR | GWD | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0215 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03669 | hp1 | a0002 | c0004 | t0001 | g0267 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03688 | hp1 | a0020 | c0040 | t0001 | g0206 | SAS | STU | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | STU | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03704 | hp1 | a0002 | c0004 | t0001 | g0266 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03831 | hp1 | a0002 | c0004 | t0001 | g0049 | SAS | BEB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | BEB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03927 | hp1 | a0042 | c0052 | t0001 | g0079 | SAS | BEB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | BEB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0183 | SAS | BEB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0189 | SAS | STU | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | STU | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18747 | hp1 | a0012 | c0012 | t0002 | g0153 | EAS | CHB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18747 | hp2 | a0010 | c0027 | t0001 | g0135 | EAS | CHB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0242 | AFR | YRI | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | YRI | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18939 | hp1 | a0001 | c0015 | t0001 | g0064 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18939 | hp2 | a0010 | c0049 | t0001 | g0053 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18944 | hp1 | a0001 | c0015 | t0001 | g0062 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18946 | hp1 | a0001 | c0003 | t0002 | g0097 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18951 | hp2 | a0015 | c0048 | t0001 | g0096 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18956 | hp2 | a0038 | c0057 | t0003 | g0273 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18957 | hp2 | a0017 | c0016 | t0003 | g0148 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18968 | hp1 | a0002 | c0004 | t0001 | g0013 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18971 | hp1 | a0018 | c0051 | t0003 | g0289 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18972 | hp1 | a0011 | c0014 | t0001 | g0264 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18972 | hp2 | a0027 | c0028 | t0001 | g0165 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18974 | hp1 | a0002 | c0004 | t0001 | g0037 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18981 | hp1 | a0001 | c0015 | t0001 | g0063 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18986 | hp2 | a0018 | c0032 | t0002 | g0213 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18988 | hp1 | a0001 | c0003 | t0002 | g0157 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18992 | hp1 | a0002 | c0004 | t0001 | g0284 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18999 | hp1 | a0002 | c0004 | t0001 | g0052 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19001 | hp1 | a0022 | c0061 | t0002 | g0042 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19001 | hp2 | a0002 | c0004 | t0001 | g0047 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19004 | hp1 | a0012 | c0012 | t0002 | g0154 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19010 | hp2 | a0002 | c0002 | t0012 | g0221 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | LWK | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19030 | hp2 | a0041 | c0034 | t0004 | g0300 | AFR | LWK | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19060 | hp1 | a0011 | c0014 | t0001 | g0265 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19064 | hp1 | a0001 | c0003 | t0002 | g0159 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19077 | hp1 | a0001 | c0003 | t0002 | g0188 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19079 | hp2 | a0001 | c0003 | t0002 | g0222 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19081 | hp2 | a0001 | c0003 | t0002 | g0196 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19082 | hp2 | a0037 | c0058 | t0002 | g0044 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19085 | hp1 | a0001 | c0060 | t0002 | g0077 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19085 | hp2 | a0028 | c0025 | t0001 | g0202 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19240 | hp1 | a0006 | c0008 | t0001 | g0219 | AFR | YRI | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA19240 | hp2 | a0009 | c0013 | t0005 | g0100 | AFR | YRI | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | ASW | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA20129 | hp2 | a0033 | c0044 | t0001 | g0268 | AFR | ASW | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | CLM | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG01123 | hp2 | a0001 | c0011 | t0003 | g0274 | AMR | CLM | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02486 | hp1 | a0013 | c0017 | t0005 | g0101 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02486 | hp2 | a0004 | c0007 | t0001 | g0299 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02559 | hp1 | a0001 | c0003 | t0004 | g0296 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG02559 | hp2 | a0003 | c0006 | t0008 | g0236 | AFR | ACB | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0111 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG03471 | hp2 | a0021 | c0042 | t0005 | g0099 | AFR | MSL | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG06807 | hp1 | a0007 | c0009 | t0007 | g0129 | AFR | USA | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| HG06807 | hp2 | a0005 | c0005 | t0006 | g0247 | AFR | USA | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18955 | hp1 | a0001 | c0003 | t0003 | g0214 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA18955 | hp2 | a0015 | c0023 | t0001 | g0134 | EAS | JPT | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA20300 | hp1 | a0001 | c0003 | t0002 | g0131 | AFR | USA | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | USA | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | LWK | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0281 | REF | REF | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| homoSapiens_grch38 | hp1 | a0032 | c0046 | t0001 | g0092 | REF | REF | ANKRD30B_chr18_14743172_14859667 | ANKRD30B | chr18 | 14743172 | 14859667 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:14748428
|
G | T | 2 | a0044a0045 | 2 | HG01081.hp1 HG02004.hp2 |
missense_variant | MODERATE | c.9G>T | p.Arg3Ser | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/44 | 257/5335 | 9/4578 | 3/1525 | chr18 | 14748428 | ||
| chr18:14752855
|
G | A | 1 | a0019 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.353G>A | p.Arg118Lys | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/44 | 601/5335 | 353/4578 | 118/1525 | chr18 | 14752855 | ||
| chr18:14763806
|
C | T | 1 | a0020 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.941C>T | p.Ser314Phe | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/44 | 1189/5335 | 941/4578 | 314/1525 | chr18 | 14763806 | ||
| chr18:14763988
|
G | A | 4 | a0009a0013a0014others(1): Show | 8 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
missense_variant | MODERATE | c.1123G>A | p.Val375Met | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/44 | 1371/5335 | 1123/4578 | 375/1525 | chr18 | 14763988 | ||
| chr18:14764034
|
C | T | 1 | a0022 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.1169C>T | p.Thr390Ile | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/44 | 1417/5335 | 1169/4578 | 390/1525 | chr18 | 14764034 | ||
| chr18:14764088
|
A | G | 1 | a0043 | 1 | HG02622.hp1 | missense_variant&splice_region_variant | MODERATE | c.1223A>G | p.Asn408Ser | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/44 | 1471/5335 | 1223/4578 | 408/1525 | chr18 | 14764088 | ||
| chr18:14769349
|
T | A | 1 | a0023 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1232T>A | p.Val411Glu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/44 | 1480/5335 | 1232/4578 | 411/1525 | chr18 | 14769349 | ||
| chr18:14778016
|
C | G | 1 | a0024 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1361C>G | p.Thr454Arg | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/44 | 1609/5335 | 1361/4578 | 454/1525 | chr18 | 14778016 | ||
| chr18:14779970
|
C | G | 17 | a0001a0012a0016others(14): Show | 164 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(161): Show |
missense_variant | MODERATE | c.1431C>G | p.Phe477Leu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/44 | 1679/5335 | 1431/4578 | 477/1525 | chr18 | 14779970 | ||
| chr18:14784469
|
G | A | 1 | a0016 | 2 | HG00609.hp1 HG02165.hp1 |
missense_variant | MODERATE | c.1606G>A | p.Val536Ile | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/44 | 1854/5335 | 1606/4578 | 536/1525 | chr18 | 14784469 | ||
| chr18:14791404
|
C | T | 1 | a0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
missense_variant | MODERATE | c.1738C>T | p.Pro580Ser | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 1986/5335 | 1738/4578 | 580/1525 | chr18 | 14791404 | ||
| chr18:14791405
|
C | T | 1 | a0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
missense_variant | MODERATE | c.1739C>T | p.Pro580Leu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 1987/5335 | 1739/4578 | 580/1525 | chr18 | 14791405 | ||
| chr18:14791407
|
T | C | 1 | a0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
missense_variant | MODERATE | c.1741T>C | p.Cys581Arg | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 1989/5335 | 1741/4578 | 581/1525 | chr18 | 14791407 | ||
| chr18:14791408
|
G | T | 1 | a0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
missense_variant | MODERATE | c.1742G>T | p.Cys581Phe | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 1990/5335 | 1742/4578 | 581/1525 | chr18 | 14791408 | ||
| chr18:14791413
|
A | G | 1 | a0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
missense_variant | MODERATE | c.1747A>G | p.Thr583Ala | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 1995/5335 | 1747/4578 | 583/1525 | chr18 | 14791413 | ||
| chr18:14791416
|
G | C | 1 | a0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
missense_variant | MODERATE | c.1750G>C | p.Val584Leu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 1998/5335 | 1750/4578 | 584/1525 | chr18 | 14791416 | ||
| chr18:14791420
|
C | T | 1 | a0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
missense_variant | MODERATE | c.1754C>T | p.Ser585Leu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 2002/5335 | 1754/4578 | 585/1525 | chr18 | 14791420 | ||
| chr18:14791427
|
G | T | 1 | a0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
missense_variant | MODERATE | c.1761G>T | p.Lys587Asn | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 2009/5335 | 1761/4578 | 587/1525 | chr18 | 14791427 | ||
| chr18:14791435
|
A | G | 1 | a0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
missense_variant | MODERATE | c.1769A>G | p.Tyr590Cys | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 2017/5335 | 1769/4578 | 590/1525 | chr18 | 14791435 | ||
| chr18:14800232
|
GCAAACAA others(10880): Show |
G | 1 | a0009 | 3 | HG02647.hp1 HG03098.hp1 NA19240.hp2 |
exon_loss_variant | HIGH | c.2131+1068_2488+106 others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/44 | INFO_REALIGN_3_PRIME | chr18 | 14800232 | |||||
| chr18:14803118
|
ATTTCTTT others(10885): Show |
A | 1 | a0025 | 1 | HG01928.hp1 | exon_loss_variant | HIGH | c.2194-609_2551-605d others(2): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/44 | INFO_REALIGN_3_PRIME | chr18 | 14803118 | |||||
| chr18:14803746
|
A | G | 34 | a0001a0002a0003others(31): Show | 292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
missense_variant | MODERATE | c.2206A>G | p.Thr736Ala | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/44 | 2454/5335 | 2206/4578 | 736/1525 | chr18 | 14803746 | ||
| chr18:14803765
|
T | G | 15 | a0002a0003a0005others(12): Show | 121 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(118): Show |
missense_variant | MODERATE | c.2225T>G | p.Val742Gly | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/44 | 2473/5335 | 2225/4578 | 742/1525 | chr18 | 14803765 | ||
| chr18:14803765
|
TGTGTTTA others(10880): Show |
T | 3 | a0015a0031a0042 | 4 | HG03139.hp1 HG03927.hp1 NA18951.hp2 others(1): Show |
exon_loss_variant | HIGH | c.2284+736_2641+735d others(2): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 25/44 | INFO_REALIGN_3_PRIME | chr18 | 14803765 | |||||
| chr18:14803778
|
G | C | 1 | a0007 | 4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
missense_variant | MODERATE | c.2238G>C | p.Lys746Asn | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/44 | 2486/5335 | 2238/4578 | 746/1525 | chr18 | 14803778 | ||
| chr18:14808559
|
G | A | 1 | a0029 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.2293G>A | p.Asp765Asn | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 25/44 | 2541/5335 | 2293/4578 | 765/1525 | chr18 | 14808559 | ||
| chr18:14809991
|
C | T | 1 | a0011 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
missense_variant | MODERATE | c.2392C>T | p.Pro798Ser | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 27/44 | 2640/5335 | 2392/4578 | 798/1525 | chr18 | 14809991 | ||
| chr18:14810118
|
T | G | 1 | a0035 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.2426T>G | p.Val809Gly | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/44 | 2674/5335 | 2426/4578 | 809/1525 | chr18 | 14810118 | ||
| chr18:14810129
|
T | C | 1 | a0021 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.2437T>C | p.Ser813Pro | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/44 | 2685/5335 | 2437/4578 | 813/1525 | chr18 | 14810129 | ||
| chr18:14810173
|
A | C | 1 | a0026 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.2481A>C | p.Leu827Phe | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/44 | 2729/5335 | 2481/4578 | 827/1525 | chr18 | 14810173 | ||
| chr18:14813125
|
C | T | 1 | a0036 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.2510C>T | p.Ser837Phe | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/44 | 2758/5335 | 2510/4578 | 837/1525 | chr18 | 14813125 | ||
| chr18:14814633
|
G | A | 33 | a0001a0002a0003others(30): Show | 293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
missense_variant | MODERATE | c.2563G>A | p.Ala855Thr | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/44 | 2811/5335 | 2563/4578 | 855/1525 | chr18 | 14814633 | ||
| chr18:14814633
|
G | GCTCTCTT others(10879): Show |
1 | a0037 | 1 | NA19082.hp2 | frameshift_variant&stop_gained | HIGH | c.2581_2582insTGTGTT others(10880): Show |
p.Gly861fs | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/44 | 2830/5335 | 2582/4578 | 861/1525 | INFO_REALIGN_3_PRIME | chr18 | 14814633 | |
| chr18:14814652
|
G | T | 38 | a0001a0002a0003others(35): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
missense_variant | MODERATE | c.2582G>T | p.Gly861Val | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/44 | 2830/5335 | 2582/4578 | 861/1525 | chr18 | 14814652 | ||
| chr18:14828290
|
C | T | 1 | a0038 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.2756C>T | p.Ser919Phe | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/44 | 3004/5335 | 2756/4578 | 919/1525 | chr18 | 14828290 | ||
| chr18:14837247
|
C | T | 1 | a0004 | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
missense_variant | MODERATE | c.2884C>T | p.Arg962Cys | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 35/44 | 3132/5335 | 2884/4578 | 962/1525 | chr18 | 14837247 | ||
| chr18:14843024
|
C | G | 1 | a0039 | 1 | HG01515.hp1 | missense_variant&splice_region_variant | MODERATE | c.3109C>G | p.Pro1037Ala | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/44 | 3357/5335 | 3109/4578 | 1037/1525 | chr18 | 14843024 | ||
| chr18:14848749
|
T | C | 5 | a0008a0009a0021others(2): Show | 10 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.3215T>C | p.Leu1072Pro | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/44 | 3463/5335 | 3215/4578 | 1072/1525 | chr18 | 14848749 | ||
| chr18:14848821
|
C | T | 12 | a0002a0010a0015others(9): Show | 103 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(100): Show |
missense_variant | MODERATE | c.3287C>T | p.Thr1096Met | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/44 | 3535/5335 | 3287/4578 | 1096/1525 | chr18 | 14848821 | ||
| chr18:14851675
|
A | T | 1 | a0028 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.3731A>T | p.Glu1244Val | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/44 | 3979/5335 | 3731/4578 | 1244/1525 | chr18 | 14851675 | ||
| chr18:14851921
|
G | T | 1 | a0041 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.3977G>T | p.Gly1326Val | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/44 | 4225/5335 | 3977/4578 | 1326/1525 | chr18 | 14851921 | ||
| chr18:14852336
|
C | A | 40 | a0001a0002a0004others(37): Show | 304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
missense_variant | MODERATE | c.4392C>A | p.Asn1464Lys | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/44 | 4640/5335 | 4392/4578 | 1464/1525 | chr18 | 14852336 | ||
| chr18:14852398
|
A | G | 1 | a0040 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.4454A>G | p.Glu1485Gly | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/44 | 4702/5335 | 4454/4578 | 1485/1525 | chr18 | 14852398 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:14748464
|
G | T | 1 | a0001c0063 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.45G>T | p.Pro15Pro | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/44 | 293/5335 | 45/4578 | 15/1525 | chr18 | 14748464 | ||
| chr18:14752958
|
G | A | 32 | a0001c0003a0001c0036a0001c0037others(29): Show | 156 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(153): Show |
synonymous_variant | LOW | c.456G>A | p.Leu152Leu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/44 | 704/5335 | 456/4578 | 152/1525 | chr18 | 14752958 | ||
| chr18:14752997
|
C | T | 1 | a0030c0062 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.495C>T | p.Ile165Ile | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/44 | 743/5335 | 495/4578 | 165/1525 | chr18 | 14752997 | ||
| chr18:14754959
|
T | C | 1 | a0001c0041 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.571T>C | p.Leu191Leu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/44 | 819/5335 | 571/4578 | 191/1525 | chr18 | 14754959 | ||
| chr18:14763993
|
A | G | 1 | a0001c0015 | 3 | NA18939.hp1 NA18944.hp1 NA18981.hp1 |
synonymous_variant | LOW | c.1128A>G | p.Ala376Ala | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/44 | 1376/5335 | 1128/4578 | 376/1525 | chr18 | 14763993 | ||
| chr18:14778017
|
G | A | 1 | a0003c0021 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.1362G>A | p.Thr454Thr | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/44 | 1610/5335 | 1362/4578 | 454/1525 | chr18 | 14778017 | ||
| chr18:14791415
|
G | T | 1 | a0012c0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
synonymous_variant | LOW | c.1749G>T | p.Thr583Thr | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 1997/5335 | 1749/4578 | 583/1525 | chr18 | 14791415 | ||
| chr18:14791418
|
T | C | 1 | a0012c0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
synonymous_variant | LOW | c.1752T>C | p.Val584Val | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 2000/5335 | 1752/4578 | 584/1525 | chr18 | 14791418 | ||
| chr18:14791445
|
A | G | 1 | a0012c0012 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
synonymous_variant | LOW | c.1779A>G | p.Lys593Lys | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/44 | 2027/5335 | 1779/4578 | 593/1525 | chr18 | 14791445 | ||
| chr18:14808740
|
A | G | 1 | a0001c0060 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.2382A>G | p.Lys794Lys | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/44 | 2630/5335 | 2382/4578 | 794/1525 | chr18 | 14808740 | ||
| chr18:14810152
|
A | G | 1 | a0021c0042 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.2460A>G | p.Glu820Glu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/44 | 2708/5335 | 2460/4578 | 820/1525 | chr18 | 14810152 | ||
| chr18:14810173
|
A | G | 2 | a0001c0011a0001c0037 | 5 | HG00735.hp1 HG01123.hp2 HG01978.hp2 others(2): Show |
synonymous_variant | LOW | c.2481A>G | p.Leu827Leu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/44 | 2729/5335 | 2481/4578 | 827/1525 | chr18 | 14810173 | ||
| chr18:14810179
|
A | C | 2 | a0001c0036a0001c0059 | 2 | HG00099.hp2 HG01243.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2487A>C | p.Ala829Ala | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/44 | 2735/5335 | 2487/4578 | 829/1525 | chr18 | 14810179 | ||
| chr18:14831449
|
T | C | 1 | a0035c0054 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.2841T>C | p.Thr947Thr | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/44 | 3089/5335 | 2841/4578 | 947/1525 | chr18 | 14831449 | ||
| chr18:14831452
|
C | T | 1 | a0004c0007 | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
synonymous_variant | LOW | c.2844C>T | p.Thr948Thr | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/44 | 3092/5335 | 2844/4578 | 948/1525 | chr18 | 14831452 | ||
| chr18:14848822
|
G | A | 29 | a0001c0001a0001c0003a0001c0011others(26): Show | 168 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
synonymous_variant | LOW | c.3288G>A | p.Thr1096Thr | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/44 | 3536/5335 | 3288/4578 | 1096/1525 | chr18 | 14848822 | ||
| chr18:14850238
|
G | A | 3 | a0004c0007a0004c0022a0004c0045 | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
synonymous_variant | LOW | c.3420G>A | p.Glu1140Glu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/44 | 3668/5335 | 3420/4578 | 1140/1525 | chr18 | 14850238 | ||
| chr18:14850253
|
C | T | 3 | a0008c0010a0023c0043a0031c0047 | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
synonymous_variant | LOW | c.3435C>T | p.Val1145Val | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/44 | 3683/5335 | 3435/4578 | 1145/1525 | chr18 | 14850253 | ||
| chr18:14850376
|
G | A | 29 | a0001c0001a0001c0003a0001c0011others(26): Show | 168 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
synonymous_variant | LOW | c.3558G>A | p.Leu1186Leu | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/44 | 3806/5335 | 3558/4578 | 1186/1525 | chr18 | 14850376 | ||
| chr18:14851757
|
G | A | 37 | a0001c0001a0001c0003a0001c0011others(34): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
synonymous_variant | LOW | c.3813G>A | p.Thr1271Thr | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/44 | 4061/5335 | 3813/4578 | 1271/1525 | chr18 | 14851757 | ||
| chr18:14853841
|
G | T | 63 | a0001c0001a0001c0003a0001c0011others(60): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
synonymous_variant | LOW | c.4509G>T | p.Ala1503Ala | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 43/44 | 4757/5335 | 4509/4578 | 1503/1525 | chr18 | 14853841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:14748172
|
G | C | 1 | a0001c0001t0011 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-248G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/44 | 248 | chr18 | 14748172 | |||||
| chr18:14748194
|
G | T | 5 | a0001c0001t0013a0009c0013t0005a0013c0017t0005others(2): Show | 8 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-226G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/44 | 226 | chr18 | 14748194 | |||||
| chr18:14748217
|
C | T | 2 | a0004c0045t0010a0034c0053t0010 | 2 | HG02818.hp1 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-203C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/44 | 203 | chr18 | 14748217 | |||||
| chr18:14748256
|
C | G | 3 | a0003c0006t0008a0008c0010t0008a0024c0038t0008 | 4 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-164C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/44 | 164 | chr18 | 14748256 | |||||
| chr18:14748377
|
G | A | 1 | a0005c0005t0006 | 5 | HG02280.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-43G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/44 | 43 | chr18 | 14748377 | |||||
| chr18:14748392
|
G | A | 3 | a0001c0003t0009a0007c0009t0007a0043c0039t0009 | 7 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-28G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/44 | 28 | chr18 | 14748392 | |||||
| chr18:14854381
|
G | A | 12 | a0001c0001t0003a0001c0001t0013a0001c0003t0003others(9): Show | 32 | HG00609.hp1 HG00735.hp1 HG01106.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*223G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 44/44 | 471 | chr18 | 14854381 | |||||
| chr18:14854453
|
C | T | 7 | a0001c0001t0004a0001c0003t0004a0001c0063t0004others(4): Show | 15 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*295C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 44/44 | 543 | chr18 | 14854453 | |||||
| chr18:14854458
|
G | C | 1 | a0002c0002t0012 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*300G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 44/44 | 548 | chr18 | 14854458 | |||||
| chr18:14854485
|
C | T | 16 | a0001c0001t0002a0001c0001t0004a0001c0003t0002others(13): Show | 82 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*327C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 44/44 | 575 | chr18 | 14854485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:14748713
|
T | G | 2 | a0008c0010t0008g0006a0008c0010t0008g0007 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.221+73T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14748713 | ||||||
| chr18:14748889
|
G | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(31): Show | 35 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.221+249G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14748889 | ||||||
| chr18:14748927
|
C | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(252): Show | 261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.221+287C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14748927 | ||||||
| chr18:14749256
|
A | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(31): Show | 35 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.221+616A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749256 | ||||||
| chr18:14749327
|
T | C | 45 | a0001c0001t0002g0041a0001c0001t0002g0043a0001c0001t0002g0045others(42): Show | 45 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.221+687T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749327 | ||||||
| chr18:14749369
|
G | T | 18 | a0001c0003t0004g0295a0001c0003t0004g0296a0001c0003t0004g0298others(15): Show | 19 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.221+729G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749369 | ||||||
| chr18:14749409
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0252a0001c0001t0001g0253others(44): Show | 50 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.221+769C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749409 | ||||||
| chr18:14749474
|
C | A | 1 | a0001c0001t0002g0041 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.221+834C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749474 | ||||||
| chr18:14749501
|
G | C | 2 | a0001c0003t0002g0097a0002c0002t0001g0098 | 2 | NA18946.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.221+861G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749501 | ||||||
| chr18:14749506
|
T | C | 9 | a0008c0010t0008g0006a0008c0010t0008g0007a0009c0013t0005g0100others(6): Show | 9 | HG02486.hp1 HG02615.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.221+866T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749506 | ||||||
| chr18:14749576
|
C | T | 1 | a0002c0002t0001g0248 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.221+936C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749576 | ||||||
| chr18:14749670
|
C | CA | 10 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0068others(7): Show | 10 | HG02683.hp1 HG02735.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.221+1062dupA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14749670 | |||||
| chr18:14749670
|
C | CAA | 21 | a0001c0001t0002g0041a0001c0001t0002g0051a0001c0001t0002g0054others(18): Show | 21 | HG00423.hp1 HG00609.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.221+1061_221+1062d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14749670 | |||||
| chr18:14749670
|
C | CAAA | 9 | a0001c0001t0002g0043a0001c0001t0002g0045a0001c0001t0002g0046others(6): Show | 9 | HG02040.hp1 HG02145.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.221+1060_221+1062d others(5): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14749670 | |||||
| chr18:14749670
|
CAAAAAA | C | 23 | a0001c0001t0002g0110a0001c0003t0001g0120a0001c0003t0001g0125others(20): Show | 23 | HG01069.hp2 HG01074.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.221+1057_221+1062d others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14749670 | |||||
| chr18:14749670
|
CAAAAAAA | C | 105 | a0001c0001t0001g0008a0001c0003t0001g0186a0001c0003t0001g0193others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.221+1056_221+1062d others(9): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14749670 | |||||
| chr18:14749670
|
CAAAAAAA others(1): Show |
C | 24 | a0001c0001t0001g0011a0001c0001t0002g0010a0001c0001t0002g0012others(21): Show | 25 | HG01993.hp1 HG02055.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.221+1055_221+1062d others(10): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14749670 | |||||
| chr18:14749670
|
CAAAAAAA others(2): Show |
C | 46 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(43): Show | 48 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.221+1054_221+1062d others(11): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14749670 | |||||
| chr18:14749670
|
CAAAAAAA others(3): Show |
C | 54 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0040others(51): Show | 57 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.221+1053_221+1062d others(12): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14749670 | |||||
| chr18:14749670
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0293a0001c0001t0002g0084 | 2 | HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.221+1052_221+1062d others(13): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14749670 | |||||
| chr18:14749708
|
G | C | 14 | a0001c0003t0004g0295a0001c0003t0004g0296a0001c0003t0004g0298others(11): Show | 14 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.221+1068G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749708 | ||||||
| chr18:14749882
|
A | G | 1 | a0004c0007t0001g0310 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.221+1242A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749882 | ||||||
| chr18:14749901
|
A | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(31): Show | 35 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.221+1261A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749901 | ||||||
| chr18:14749971
|
A | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0252a0001c0001t0001g0253others(44): Show | 50 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.221+1331A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14749971 | ||||||
| chr18:14750119
|
T | C | 10 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(7): Show | 10 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.221+1479T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14750119 | ||||||
| chr18:14750170
|
A | G | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.221+1530A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14750170 | ||||||
| chr18:14750248
|
C | A | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.221+1608C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14750248 | ||||||
| chr18:14750329
|
G | T | 1 | a0001c0003t0004g0298 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.221+1689G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14750329 | ||||||
| chr18:14750546
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(251): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.221+1906A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14750546 | ||||||
| chr18:14750678
|
T | G | 1 | a0001c0003t0004g0244 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.222-1888T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14750678 | ||||||
| chr18:14750686
|
T | A | 1 | a0001c0001t0002g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.222-1880T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14750686 | ||||||
| chr18:14750720
|
G | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0023others(29): Show | 33 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.222-1846G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14750720 | ||||||
| chr18:14750848
|
T | C | 128 | a0001c0001t0002g0110a0001c0003t0001g0120a0001c0003t0001g0125others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.222-1718T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14750848 | ||||||
| chr18:14751050
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0252a0001c0001t0001g0253others(53): Show | 59 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.222-1516T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751050 | ||||||
| chr18:14751280
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0252a0001c0001t0001g0253others(53): Show | 59 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.222-1286A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751280 | ||||||
| chr18:14751293
|
C | T | 1 | a0002c0002t0001g0225 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.222-1273C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751293 | ||||||
| chr18:14751438
|
G | A | 128 | a0001c0001t0002g0110a0001c0003t0001g0120a0001c0003t0001g0125others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.222-1128G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751438 | ||||||
| chr18:14751465
|
A | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0023others(29): Show | 33 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.222-1101A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751465 | ||||||
| chr18:14751490
|
G | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(251): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.222-1076G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751490 | ||||||
| chr18:14751547
|
G | GT | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.222-1015dupT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14751547 | |||||
| chr18:14751547
|
G | T | 1 | a0001c0003t0002g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.222-1019G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751547 | ||||||
| chr18:14751599
|
C | T | 1 | a0001c0001t0002g0020 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.222-967C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751599 | ||||||
| chr18:14751623
|
C | T | 2 | a0001c0001t0001g0008a0013c0017t0001g0009 | 2 | HG01167.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.222-943C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751623 | ||||||
| chr18:14751627
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.222-939A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751627 | ||||||
| chr18:14751694
|
A | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(251): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.222-872A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751694 | ||||||
| chr18:14751771
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0252a0001c0001t0001g0253others(44): Show | 50 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.222-795A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751771 | ||||||
| chr18:14751807
|
T | C | 7 | a0001c0003t0009g0228a0001c0003t0009g0229a0007c0009t0007g0128others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-759T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751807 | ||||||
| chr18:14751845
|
G | A | 1 | a0001c0003t0004g0244 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.222-721G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751845 | ||||||
| chr18:14751864
|
AT | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.222-700delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14751864 | |||||
| chr18:14751866
|
T | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.222-700T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751866 | ||||||
| chr18:14751946
|
A | C | 2 | a0001c0001t0001g0008a0013c0017t0001g0009 | 2 | HG01167.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.222-620A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14751946 | ||||||
| chr18:14752273
|
G | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(302): Show | 311 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.222-293G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14752273 | ||||||
| chr18:14752274
|
C | T | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-292C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14752274 | ||||||
| chr18:14752347
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.222-219G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | chr18 | 14752347 | ||||||
| chr18:14752482
|
AT | A | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-81delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr18 | 14752482 | |||||
| chr18:14752740
|
A | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0023others(32): Show | 36 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.336+60A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 2/43 | chr18 | 14752740 | ||||||
| chr18:14752769
|
G | A | 142 | a0001c0001t0002g0110a0001c0003t0001g0120a0001c0003t0001g0125others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.337-70G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 2/43 | chr18 | 14752769 | ||||||
| chr18:14753401
|
C | G | 1 | a0001c0001t0001g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.510+389C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753401 | ||||||
| chr18:14753436
|
G | C | 170 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0023others(167): Show | 173 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.510+424G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753436 | ||||||
| chr18:14753475
|
C | T | 2 | a0002c0002t0001g0197a0002c0002t0001g0198 | 2 | HG02523.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.510+463C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753475 | ||||||
| chr18:14753512
|
C | T | 41 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(38): Show | 41 | HG01167.hp2 HG01243.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+500C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753512 | ||||||
| chr18:14753513
|
C | T | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.510+501C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753513 | ||||||
| chr18:14753533
|
T | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0253others(24): Show | 29 | HG00544.hp2 HG00738.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.510+521T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753533 | ||||||
| chr18:14753566
|
T | C | 150 | a0001c0001t0001g0008a0001c0001t0001g0277a0001c0001t0002g0012others(147): Show | 152 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.510+554T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753566 | ||||||
| chr18:14753602
|
G | C | 42 | a0001c0001t0002g0065a0001c0003t0002g0151a0001c0003t0002g0155others(39): Show | 42 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.510+590G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753602 | ||||||
| chr18:14753669
|
C | T | 1 | a0023c0043t0001g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.510+657C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753669 | ||||||
| chr18:14753892
|
G | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.510+880G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753892 | ||||||
| chr18:14753936
|
GTAGCAAT others(5): Show |
G | 4 | a0001c0055t0001g0088a0011c0014t0001g0086a0011c0014t0001g0264others(1): Show | 4 | HG02145.hp2 HG03209.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+931_510+942del others(12): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr18 | 14753936 | |||||
| chr18:14753966
|
A | C | 3 | a0001c0003t0002g0196a0001c0003t0002g0222a0002c0002t0012g0221 | 3 | NA19010.hp2 NA19079.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.511-933A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14753966 | ||||||
| chr18:14754243
|
G | C | 3 | a0001c0003t0004g0303a0005c0005t0001g0302a0040c0033t0004g0304 | 3 | HG02723.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.511-656G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14754243 | ||||||
| chr18:14754442
|
T | C | 2 | a0001c0001t0002g0078a0001c0060t0002g0077 | 2 | NA18973.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.511-457T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14754442 | ||||||
| chr18:14754548
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(99): Show | 105 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.511-351C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14754548 | ||||||
| chr18:14754606
|
C | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(95): Show | 101 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.511-293C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14754606 | ||||||
| chr18:14754706
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.511-193G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14754706 | ||||||
| chr18:14754768
|
G | A | 1 | a0001c0001t0003g0269 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.511-131G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 3/43 | chr18 | 14754768 | ||||||
| chr18:14755163
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.617+158G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755163 | ||||||
| chr18:14755420
|
T | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(95): Show | 101 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.617+415T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755420 | ||||||
| chr18:14755446
|
T | C | 5 | a0001c0001t0002g0110a0001c0003t0002g0106a0001c0003t0002g0111others(2): Show | 5 | HG01074.hp2 HG01109.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+441T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755446 | ||||||
| chr18:14755446
|
T | G | 1 | a0001c0011t0003g0270 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.617+441T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755446 | ||||||
| chr18:14755472
|
G | A | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.617+467G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755472 | ||||||
| chr18:14755488
|
G | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(297): Show | 305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.617+483G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755488 | ||||||
| chr18:14755521
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(92): Show | 98 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.617+516G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755521 | ||||||
| chr18:14755673
|
G | A | 4 | a0001c0055t0001g0088a0011c0014t0001g0086a0011c0014t0001g0264others(1): Show | 4 | HG02145.hp2 HG03209.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+668G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755673 | ||||||
| chr18:14755885
|
G | A | 4 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(1): Show | 4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+880G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755885 | ||||||
| chr18:14755907
|
G | A | 1 | a0002c0004t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.617+902G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755907 | ||||||
| chr18:14755973
|
C | T | 2 | a0001c0003t0004g0307a0001c0003t0004g0308 | 2 | HG01167.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.617+968C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755973 | ||||||
| chr18:14755974
|
G | A | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+969G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755974 | ||||||
| chr18:14755978
|
C | T | 1 | a0006c0008t0001g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.617+973C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755978 | ||||||
| chr18:14755982
|
G | A | 5 | a0009c0013t0005g0104a0009c0013t0005g0105a0013c0017t0005g0101others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+977G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755982 | ||||||
| chr18:14755990
|
C | G | 8 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+985C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14755990 | ||||||
| chr18:14756027
|
A | C | 1 | a0002c0002t0001g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.617+1022A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756027 | ||||||
| chr18:14756190
|
C | T | 8 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+1185C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756190 | ||||||
| chr18:14756203
|
T | C | 1 | a0002c0002t0001g0158 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.617+1198T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756203 | ||||||
| chr18:14756227
|
C | T | 4 | a0001c0001t0001g0008a0008c0010t0008g0006a0008c0010t0008g0007others(1): Show | 4 | HG01167.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+1222C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756227 | ||||||
| chr18:14756275
|
T | C | 8 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+1270T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756275 | ||||||
| chr18:14756464
|
T | C | 3 | a0005c0005t0006g0245a0005c0005t0006g0246a0005c0005t0006g0247 | 3 | HG02280.hp2 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.618-1351T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756464 | ||||||
| chr18:14756465
|
G | A | 3 | a0005c0005t0006g0245a0005c0005t0006g0246a0005c0005t0006g0247 | 3 | HG02280.hp2 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.618-1350G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756465 | ||||||
| chr18:14756505
|
C | A | 5 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0084others(2): Show | 5 | HG00099.hp2 HG01243.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-1310C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756505 | ||||||
| chr18:14756522
|
G | C | 1 | a0001c0001t0002g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.618-1293G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756522 | ||||||
| chr18:14756582
|
C | G | 3 | a0001c0003t0004g0298a0036c0035t0004g0306a0041c0034t0004g0300 | 3 | HG02055.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.618-1233C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756582 | ||||||
| chr18:14756587
|
T | C | 33 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(30): Show | 34 | HG01167.hp2 HG02055.hp2 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.618-1228T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756587 | ||||||
| chr18:14756607
|
A | G | 1 | a0036c0035t0004g0306 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.618-1208A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756607 | ||||||
| chr18:14756667
|
T | C | 2 | a0001c0001t0002g0045a0037c0058t0002g0044 | 2 | NA19082.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.618-1148T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756667 | ||||||
| chr18:14756722
|
C | T | 4 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(1): Show | 4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-1093C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756722 | ||||||
| chr18:14756807
|
G | A | 2 | a0011c0014t0001g0264a0011c0014t0001g0265 | 2 | NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.618-1008G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756807 | ||||||
| chr18:14756809
|
T | C | 1 | a0042c0052t0001g0079 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.618-1006T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756809 | ||||||
| chr18:14756836
|
G | A | 1 | a0010c0026t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.618-979G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756836 | ||||||
| chr18:14756917
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.618-898T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14756917 | ||||||
| chr18:14757058
|
AT | A | 7 | a0001c0001t0001g0256a0001c0001t0001g0292a0001c0003t0002g0131others(4): Show | 7 | HG00544.hp2 HG01106.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-750delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr18 | 14757058 | |||||
| chr18:14757247
|
T | A | 1 | a0001c0001t0002g0041 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.618-568T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14757247 | ||||||
| chr18:14757275
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(128): Show | 135 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.618-540G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14757275 | ||||||
| chr18:14757633
|
A | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(95): Show | 101 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.618-182A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14757633 | ||||||
| chr18:14757639
|
G | A | 33 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(30): Show | 34 | HG01167.hp2 HG02055.hp2 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.618-176G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14757639 | ||||||
| chr18:14757767
|
A | G | 4 | a0001c0001t0001g0292a0001c0003t0002g0131a0002c0002t0001g0130others(1): Show | 4 | HG00544.hp2 HG01517.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-48A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 4/43 | chr18 | 14757767 | ||||||
| chr18:14758407
|
A | G | 21 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(18): Show | 22 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.755+455A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14758407 | ||||||
| chr18:14758412
|
T | C | 1 | a0005c0005t0001g0302 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.755+460T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14758412 | ||||||
| chr18:14758417
|
T | C | 2 | a0001c0001t0002g0069a0001c0003t0002g0159 | 2 | NA18962.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.755+465T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14758417 | ||||||
| chr18:14758442
|
G | T | 4 | a0001c0001t0001g0008a0008c0010t0008g0006a0008c0010t0008g0007others(1): Show | 4 | HG01167.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.755+490G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14758442 | ||||||
| chr18:14758444
|
C | T | 8 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.755+492C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14758444 | ||||||
| chr18:14758445
|
C | T | 4 | a0001c0001t0001g0008a0008c0010t0008g0006a0008c0010t0008g0007others(1): Show | 4 | HG01167.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.755+493C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14758445 | ||||||
| chr18:14758541
|
C | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(297): Show | 305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.755+589C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14758541 | ||||||
| chr18:14758706
|
G | A | 1 | a0002c0004t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.755+754G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14758706 | ||||||
| chr18:14758836
|
T | A | 2 | a0001c0003t0009g0228a0001c0003t0009g0229 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.755+884T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14758836 | ||||||
| chr18:14758927
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(95): Show | 101 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.755+975C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14758927 | ||||||
| chr18:14759245
|
G | C | 120 | a0001c0001t0002g0012a0001c0001t0002g0065a0001c0001t0002g0110others(117): Show | 121 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.755+1293G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14759245 | ||||||
| chr18:14759574
|
C | T | 2 | a0001c0001t0002g0045a0037c0058t0002g0044 | 2 | NA19082.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.756-980C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14759574 | ||||||
| chr18:14759686
|
G | T | 120 | a0001c0001t0002g0012a0001c0001t0002g0065a0001c0001t0002g0110others(117): Show | 121 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.756-868G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14759686 | ||||||
| chr18:14759696
|
T | C | 1 | a0035c0054t0001g0258 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.756-858T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14759696 | ||||||
| chr18:14759789
|
T | C | 1 | a0001c0001t0002g0015 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.756-765T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14759789 | ||||||
| chr18:14759791
|
C | T | 1 | a0023c0043t0001g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.756-763C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14759791 | ||||||
| chr18:14759900
|
T | A | 2 | a0001c0001t0003g0269a0001c0001t0003g0271 | 2 | NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.756-654T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14759900 | ||||||
| chr18:14759990
|
T | A | 2 | a0001c0001t0002g0276a0001c0001t0003g0275 | 2 | HG01106.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.756-564T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14759990 | ||||||
| chr18:14760120
|
A | C | 3 | a0001c0015t0001g0062a0001c0015t0001g0063a0001c0015t0001g0064 | 3 | NA18939.hp1 NA18944.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.756-434A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14760120 | ||||||
| chr18:14760266
|
A | G | 1 | a0002c0002t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.756-288A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14760266 | ||||||
| chr18:14760450
|
A | G | 1 | a0001c0063t0004g0297 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.756-104A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14760450 | ||||||
| chr18:14760474
|
C | CT | 3 | a0001c0003t0001g0125a0001c0003t0001g0126a0001c0003t0001g0127 | 3 | HG01069.hp2 HG01192.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.756-79dupT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | INFO_REALIGN_3_PRIME | chr18 | 14760474 | |||||
| chr18:14760501
|
T | G | 1 | a0002c0002t0001g0132 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.756-53T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 5/43 | chr18 | 14760501 | ||||||
| chr18:14760647
|
G | T | 3 | a0001c0001t0003g0241a0001c0001t0003g0243a0001c0001t0013g0242 | 3 | HG02145.hp1 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.820+29G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14760647 | ||||||
| chr18:14760991
|
A | G | 2 | a0002c0002t0001g0109a0002c0002t0001g0156 | 2 | NA18994.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.820+373A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14760991 | ||||||
| chr18:14761135
|
C | T | 4 | a0001c0055t0001g0088a0011c0014t0001g0086a0011c0014t0001g0264others(1): Show | 4 | HG02145.hp2 HG03209.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+517C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14761135 | ||||||
| chr18:14761137
|
A | G | 22 | a0001c0001t0003g0087a0001c0001t0004g0290a0001c0001t0004g0291others(19): Show | 23 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.820+519A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14761137 | ||||||
| chr18:14761200
|
G | A | 1 | a0001c0003t0002g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.820+582G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14761200 | ||||||
| chr18:14761200
|
G | T | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.820+582G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14761200 | ||||||
| chr18:14761282
|
C | T | 4 | a0001c0055t0001g0088a0011c0014t0001g0086a0011c0014t0001g0264others(1): Show | 4 | HG02145.hp2 HG03209.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+664C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14761282 | ||||||
| chr18:14761464
|
AG | A | 127 | a0001c0001t0002g0012a0001c0001t0002g0065a0001c0001t0002g0110others(124): Show | 129 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.820+850delG | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr18 | 14761464 | |||||
| chr18:14761631
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0253a0001c0001t0001g0259others(5): Show | 10 | HG02572.hp1 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.820+1013G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14761631 | ||||||
| chr18:14761710
|
T | TTTTA | 4 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(1): Show | 4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820+1111_820+1114d others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr18 | 14761710 | |||||
| chr18:14762027
|
C | T | 1 | a0043c0039t0009g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.820+1409C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762027 | ||||||
| chr18:14762085
|
A | G | 41 | a0001c0001t0002g0041a0001c0001t0002g0043a0001c0001t0002g0045others(38): Show | 41 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.820+1467A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762085 | ||||||
| chr18:14762349
|
C | T | 1 | a0002c0002t0001g0215 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.821-1337C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762349 | ||||||
| chr18:14762398
|
G | C | 1 | a0001c0003t0004g0303 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.821-1288G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762398 | ||||||
| chr18:14762487
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(103): Show | 109 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.821-1199G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762487 | ||||||
| chr18:14762648
|
C | A | 1 | a0001c0001t0003g0272 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.821-1038C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762648 | ||||||
| chr18:14762657
|
A | G | 2 | a0001c0001t0003g0085a0001c0001t0003g0087 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.821-1029A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762657 | ||||||
| chr18:14762729
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.821-957A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762729 | ||||||
| chr18:14762769
|
G | A | 1 | a0031c0047t0001g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.821-917G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762769 | ||||||
| chr18:14762808
|
T | C | 4 | a0002c0002t0001g0107a0002c0002t0001g0133a0002c0004t0001g0076others(1): Show | 4 | HG00544.hp1 HG00673.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-878T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762808 | ||||||
| chr18:14762911
|
G | T | 4 | a0001c0001t0001g0008a0008c0010t0008g0006a0008c0010t0008g0007others(1): Show | 4 | HG01167.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-775G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762911 | ||||||
| chr18:14762917
|
C | G | 1 | a0001c0001t0002g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.821-769C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14762917 | ||||||
| chr18:14763096
|
T | C | 3 | a0001c0001t0003g0241a0001c0001t0003g0243a0001c0001t0013g0242 | 3 | HG02145.hp1 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.821-590T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14763096 | ||||||
| chr18:14763251
|
T | C | 8 | a0001c0001t0001g0008a0007c0009t0007g0128a0007c0009t0007g0129others(5): Show | 8 | HG01167.hp1 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.821-435T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14763251 | ||||||
| chr18:14763377
|
G | A | 4 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(1): Show | 4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.821-309G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14763377 | ||||||
| chr18:14763497
|
C | A | 20 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(17): Show | 21 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.821-189C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14763497 | ||||||
| chr18:14763524
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.821-162T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 6/43 | chr18 | 14763524 | ||||||
| chr18:14764452
|
C | T | 119 | a0001c0001t0002g0012a0001c0001t0002g0065a0001c0001t0002g0110others(116): Show | 120 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1225+362C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14764452 | ||||||
| chr18:14764479
|
C | T | 8 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1225+389C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14764479 | ||||||
| chr18:14764557
|
C | T | 116 | a0001c0001t0002g0012a0001c0001t0002g0065a0001c0001t0002g0110others(113): Show | 117 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1225+467C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14764557 | ||||||
| chr18:14764560
|
A | AT | 87 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0023others(84): Show | 88 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.1225+476dupT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14764560 | |||||
| chr18:14764637
|
C | A | 29 | a0001c0001t0001g0259a0001c0001t0004g0290a0001c0001t0004g0291others(26): Show | 30 | HG01167.hp2 HG02055.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.1225+547C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14764637 | ||||||
| chr18:14764638
|
T | G | 29 | a0001c0001t0001g0259a0001c0001t0004g0290a0001c0001t0004g0291others(26): Show | 30 | HG01167.hp2 HG02055.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.1225+548T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14764638 | ||||||
| chr18:14764665
|
G | A | 3 | a0005c0005t0001g0302a0005c0005t0006g0232a0005c0005t0006g0233 | 3 | HG02723.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1225+575G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14764665 | ||||||
| chr18:14764679
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(170): Show | 177 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.1225+589C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14764679 | ||||||
| chr18:14764759
|
G | C | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1225+669G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14764759 | ||||||
| chr18:14764952
|
G | A | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1225+862G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14764952 | ||||||
| chr18:14765115
|
C | A | 1 | a0001c0001t0002g0038 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1225+1025C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14765115 | ||||||
| chr18:14765180
|
G | A | 8 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1225+1090G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14765180 | ||||||
| chr18:14765185
|
G | A | 3 | a0002c0002t0001g0189a0002c0004t0001g0254a0002c0004t0001g0288 | 3 | HG00738.hp2 HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1225+1095G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14765185 | ||||||
| chr18:14765194
|
C | T | 1 | a0002c0002t0001g0248 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1225+1104C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14765194 | ||||||
| chr18:14765333
|
C | T | 14 | a0001c0001t0002g0276a0001c0001t0003g0269a0001c0001t0003g0271others(11): Show | 14 | HG00735.hp1 HG01106.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1225+1243C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14765333 | ||||||
| chr18:14765395
|
G | A | 1 | a0010c0026t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1225+1305G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14765395 | ||||||
| chr18:14765462
|
GA | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(169): Show | 176 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.1225+1384delA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14765462 | |||||
| chr18:14765462
|
GAA | G | 10 | a0001c0001t0002g0075a0001c0003t0004g0298a0009c0013t0005g0100others(7): Show | 10 | HG02486.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1225+1383_1225+138 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14765462 | |||||
| chr18:14765509
|
T | A | 1 | a0001c0001t0011g0022 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1225+1419T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14765509 | ||||||
| chr18:14765564
|
T | C | 1 | a0001c0011t0003g0280 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1225+1474T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14765564 | ||||||
| chr18:14765669
|
C | A | 51 | a0001c0001t0002g0033a0001c0001t0002g0041a0001c0001t0002g0043others(48): Show | 51 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1225+1579C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14765669 | ||||||
| chr18:14765747
|
CT | C | 42 | a0002c0002t0001g0107a0002c0002t0001g0109a0002c0002t0001g0122others(39): Show | 42 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1225+1666delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14765747 | |||||
| chr18:14765930
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1225+1840T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14765930 | ||||||
| chr18:14766110
|
A | G | 1 | a0002c0002t0001g0204 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1225+2020A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14766110 | ||||||
| chr18:14766434
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1225+2344C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14766434 | ||||||
| chr18:14766459
|
C | T | 1 | a0002c0002t0001g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1225+2369C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14766459 | ||||||
| chr18:14766472
|
C | CA | 137 | a0001c0001t0002g0012a0001c0001t0002g0041a0001c0001t0002g0043others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1225+2407dupA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766472 | |||||
| chr18:14766472
|
C | CAA | 17 | a0001c0001t0002g0075a0001c0003t0002g0159a0001c0003t0002g0205others(14): Show | 17 | HG00438.hp1 HG00735.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1225+2406_1225+240 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766472 | |||||
| chr18:14766472
|
CA | C | 7 | a0001c0055t0001g0088a0004c0022t0001g0301a0008c0010t0008g0006others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1225+2407delA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766472 | |||||
| chr18:14766472
|
CAA | C | 20 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0295others(17): Show | 21 | HG01167.hp2 HG01243.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1225+2406_1225+240 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766472 | |||||
| chr18:14766472
|
CAAA | C | 9 | a0001c0003t0004g0244a0009c0013t0005g0100a0009c0013t0005g0104others(6): Show | 9 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225+2405_1225+240 others(7): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766472 | |||||
| chr18:14766488
|
A | AAAGAAAG others(10): Show |
5 | a0001c0001t0001g0001a0001c0001t0001g0253a0001c0001t0001g0259others(2): Show | 7 | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1225+2400_1225+240 others(21): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766488 | |||||
| chr18:14766492
|
AAAAAAG | A | 7 | a0003c0006t0001g0003a0003c0006t0001g0237a0003c0006t0001g0240others(4): Show | 8 | HG02055.hp1 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1225+2407_1225+241 others(10): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766492 | |||||
| chr18:14766493
|
A | AAAAAGAA others(13): Show |
1 | a0043c0039t0009g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1225+2413_1225+243 others(24): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766493 | |||||
| chr18:14766493
|
A | AAAAGAAA others(12): Show |
4 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(1): Show | 4 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225+2406_1225+240 others(23): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766493 | |||||
| chr18:14766493
|
A | AAAGAAAA others(6): Show |
7 | a0001c0003t0002g0157a0001c0011t0003g0270a0001c0011t0003g0274others(4): Show | 7 | HG01123.hp2 HG02683.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225+2405_1225+240 others(17): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766493 | |||||
| chr18:14766493
|
A | AAAGAAAA others(11): Show |
30 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(27): Show | 30 | HG00609.hp1 HG00735.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1225+2405_1225+240 others(22): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766493 | |||||
| chr18:14766493
|
A | AAAGAAAA others(16): Show |
5 | a0001c0001t0001g0034a0001c0001t0002g0019a0001c0001t0002g0276others(2): Show | 5 | HG00621.hp1 HG01106.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+2405_1225+240 others(27): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766493 | |||||
| chr18:14766493
|
A | AAGAAAAG others(5): Show |
1 | a0039c0056t0001g0257 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1225+2404_1225+240 others(16): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766493 | |||||
| chr18:14766493
|
A | AAGAAAAG others(10): Show |
29 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(26): Show | 30 | HG00544.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1225+2404_1225+240 others(21): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766493 | |||||
| chr18:14766493
|
A | AAGAAAAG others(15): Show |
1 | a0001c0001t0001g0287 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1225+2404_1225+240 others(26): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766493 | |||||
| chr18:14766493
|
A | AAGAAAAG others(20): Show |
2 | a0008c0010t0001g0261a0008c0010t0001g0262 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1225+2404_1225+240 others(31): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14766493 | |||||
| chr18:14766493
|
A | AGAAAAGA others(9): Show |
2 | a0001c0001t0003g0087a0001c0001t0003g0250 | 2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1225+2403_1225+240 others(20): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14766493 | ||||||
| chr18:14766493
|
A | AGAAAAGA others(14): Show |
1 | a0001c0001t0003g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1225+2403_1225+240 others(25): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14766493 | ||||||
| chr18:14766493
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0253a0001c0001t0001g0259others(2): Show | 7 | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1225+2403A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14766493 | ||||||
| chr18:14766639
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(88): Show | 94 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1225+2549G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14766639 | ||||||
| chr18:14766873
|
A | G | 1 | a0002c0004t0001g0267 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1226-2470A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14766873 | ||||||
| chr18:14767226
|
A | G | 118 | a0001c0001t0002g0012a0001c0001t0002g0065a0001c0001t0003g0279others(115): Show | 119 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.1226-2117A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14767226 | ||||||
| chr18:14767556
|
G | A | 1 | a0001c0003t0002g0151 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1226-1787G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14767556 | ||||||
| chr18:14767569
|
G | A | 8 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(5): Show | 8 | HG01243.hp1 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1226-1774G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14767569 | ||||||
| chr18:14767710
|
G | GATGACTA | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(179): Show | 186 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1226-1630_1226-162 others(11): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr18 | 14767710 | |||||
| chr18:14767723
|
C | T | 1 | a0001c0003t0002g0151 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1226-1620C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14767723 | ||||||
| chr18:14767774
|
T | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(88): Show | 94 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1226-1569T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14767774 | ||||||
| chr18:14767917
|
T | C | 1 | a0001c0003t0002g0196 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1226-1426T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14767917 | ||||||
| chr18:14767955
|
C | A | 1 | a0002c0002t0001g0130 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1226-1388C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14767955 | ||||||
| chr18:14768196
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(88): Show | 94 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1226-1147C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14768196 | ||||||
| chr18:14768197
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(88): Show | 94 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1226-1146C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14768197 | ||||||
| chr18:14768256
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0292 | 2 | HG01167.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1226-1087C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14768256 | ||||||
| chr18:14768396
|
T | C | 4 | a0008c0010t0008g0006a0008c0010t0008g0007a0023c0043t0001g0095others(1): Show | 4 | HG01243.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226-947T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14768396 | ||||||
| chr18:14768782
|
A | G | 20 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(17): Show | 21 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1226-561A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14768782 | ||||||
| chr18:14769199
|
G | T | 1 | a0023c0043t0001g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1226-144G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14769199 | ||||||
| chr18:14769209
|
C | T | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1226-134C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 7/43 | chr18 | 14769209 | ||||||
| chr18:14769398
|
C | T | 2 | a0002c0002t0001g0181a0002c0002t0001g0182 | 2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1256+25C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14769398 | ||||||
| chr18:14769488
|
A | G | 1 | a0001c0003t0002g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1256+115A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14769488 | ||||||
| chr18:14769842
|
G | A | 4 | a0008c0010t0008g0006a0008c0010t0008g0007a0023c0043t0001g0095others(1): Show | 4 | HG01243.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256+469G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14769842 | ||||||
| chr18:14770074
|
T | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(171): Show | 178 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1256+701T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14770074 | ||||||
| chr18:14770149
|
C | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(297): Show | 305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1256+776C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14770149 | ||||||
| chr18:14770264
|
G | T | 1 | a0001c0003t0002g0188 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1256+891G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14770264 | ||||||
| chr18:14770660
|
G | T | 1 | a0002c0002t0001g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1256+1287G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14770660 | ||||||
| chr18:14770663
|
T | A | 8 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1256+1290T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14770663 | ||||||
| chr18:14770781
|
G | A | 1 | a0016c0050t0003g0059 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1257-1375G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14770781 | ||||||
| chr18:14770817
|
T | TA | 33 | a0001c0001t0001g0277a0001c0001t0004g0290a0001c0001t0004g0291others(30): Show | 34 | HG01167.hp2 HG01243.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1257-1328dupA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr18 | 14770817 | |||||
| chr18:14770856
|
C | T | 1 | a0002c0004t0001g0004 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1257-1300C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14770856 | ||||||
| chr18:14771005
|
C | T | 1 | a0002c0002t0001g0149 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1257-1151C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14771005 | ||||||
| chr18:14771047
|
T | C | 1 | a0004c0007t0001g0299 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1257-1109T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14771047 | ||||||
| chr18:14771266
|
G | A | 28 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(25): Show | 29 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1257-890G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14771266 | ||||||
| chr18:14771396
|
A | T | 20 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(17): Show | 21 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1257-760A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14771396 | ||||||
| chr18:14771477
|
C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(175): Show | 182 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1257-679C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14771477 | ||||||
| chr18:14771481
|
C | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(175): Show | 182 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1257-675C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14771481 | ||||||
| chr18:14771485
|
C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(175): Show | 182 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1257-671C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14771485 | ||||||
| chr18:14771685
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(88): Show | 94 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1257-471C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14771685 | ||||||
| chr18:14771708
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(88): Show | 94 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1257-448T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 8/43 | chr18 | 14771708 | ||||||
| chr18:14772343
|
A | C | 1 | a0009c0013t0005g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1329+115A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14772343 | ||||||
| chr18:14772384
|
GT | G | 12 | a0001c0001t0001g0293a0002c0004t0001g0037a0007c0009t0007g0128others(9): Show | 12 | HG01243.hp1 HG02258.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1329+170delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr18 | 14772384 | |||||
| chr18:14772384
|
GTT | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 163 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.1329+169_1329+170d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr18 | 14772384 | |||||
| chr18:14772384
|
GTTT | G | 11 | a0001c0001t0002g0051a0008c0010t0001g0261a0008c0010t0001g0262others(8): Show | 11 | HG00423.hp1 HG02486.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1329+168_1329+170d others(5): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr18 | 14772384 | |||||
| chr18:14772398
|
T | G | 1 | a0002c0002t0001g0183 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1329+170T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14772398 | ||||||
| chr18:14772449
|
G | A | 50 | a0001c0001t0002g0033a0001c0001t0002g0041a0001c0001t0002g0043others(47): Show | 50 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1329+221G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14772449 | ||||||
| chr18:14772709
|
G | GT | 10 | a0001c0001t0002g0045a0001c0001t0002g0056a0001c0001t0002g0057others(7): Show | 10 | HG00099.hp2 HG01175.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1329+499dupT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr18 | 14772709 | |||||
| chr18:14772709
|
GT | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(201): Show | 208 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.1329+499delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr18 | 14772709 | |||||
| chr18:14772709
|
GTT | G | 31 | a0001c0001t0001g0035a0001c0001t0003g0241a0001c0001t0003g0271others(28): Show | 32 | HG00323.hp1 HG00673.hp2 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1329+498_1329+499d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr18 | 14772709 | |||||
| chr18:14772803
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(88): Show | 94 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1329+575C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14772803 | ||||||
| chr18:14772814
|
T | C | 2 | a0001c0001t0003g0272a0018c0051t0003g0289 | 2 | NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1329+586T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14772814 | ||||||
| chr18:14772936
|
C | T | 4 | a0008c0010t0008g0006a0008c0010t0008g0007a0023c0043t0001g0095others(1): Show | 4 | HG01243.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+708C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14772936 | ||||||
| chr18:14772941
|
C | T | 4 | a0001c0055t0001g0088a0011c0014t0001g0086a0011c0014t0001g0264others(1): Show | 4 | HG02145.hp2 HG03209.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+713C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14772941 | ||||||
| chr18:14772948
|
A | T | 4 | a0001c0001t0002g0041a0001c0001t0002g0051a0001c0003t0002g0196others(1): Show | 4 | HG00423.hp1 NA18943.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+720A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14772948 | ||||||
| chr18:14773072
|
C | G | 4 | a0001c0055t0001g0088a0011c0014t0001g0086a0011c0014t0001g0264others(1): Show | 4 | HG02145.hp2 HG03209.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+844C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14773072 | ||||||
| chr18:14773231
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(89): Show | 95 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1329+1003A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14773231 | ||||||
| chr18:14773360
|
A | AG | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(179): Show | 186 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1329+1133dupG | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr18 | 14773360 | |||||
| chr18:14773362
|
A | C | 49 | a0001c0001t0002g0033a0001c0001t0002g0041a0001c0001t0002g0043others(46): Show | 49 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1329+1134A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14773362 | ||||||
| chr18:14773446
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1329+1218G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14773446 | ||||||
| chr18:14773631
|
A | G | 8 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(5): Show | 8 | HG01243.hp1 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1329+1403A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14773631 | ||||||
| chr18:14773661
|
CT | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(172): Show | 179 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1329+1447delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr18 | 14773661 | |||||
| chr18:14773664
|
T | C | 8 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(5): Show | 8 | HG02486.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1329+1436T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14773664 | ||||||
| chr18:14773873
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1329+1645C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14773873 | ||||||
| chr18:14773920
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(105): Show | 111 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1329+1692C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14773920 | ||||||
| chr18:14773981
|
G | T | 11 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0169others(8): Show | 11 | HG01123.hp1 HG01255.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1329+1753G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14773981 | ||||||
| chr18:14774124
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1329+1896C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14774124 | ||||||
| chr18:14774366
|
T | G | 1 | a0001c0001t0002g0057 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1329+2138T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14774366 | ||||||
| chr18:14774379
|
T | A | 1 | a0042c0052t0001g0079 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1329+2151T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14774379 | ||||||
| chr18:14774430
|
T | G | 114 | a0001c0037t0003g0191a0002c0002t0001g0098a0002c0002t0001g0107others(111): Show | 115 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1329+2202T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14774430 | ||||||
| chr18:14774863
|
C | G | 5 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(2): Show | 6 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1329+2635C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14774863 | ||||||
| chr18:14774867
|
C | A | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+2639C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14774867 | ||||||
| chr18:14774923
|
C | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+2695C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14774923 | ||||||
| chr18:14774953
|
C | G | 3 | a0001c0003t0004g0298a0036c0035t0004g0306a0041c0034t0004g0300 | 3 | HG02055.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1329+2725C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14774953 | ||||||
| chr18:14774982
|
A | G | 1 | a0002c0004t0001g0284 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1329+2754A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14774982 | ||||||
| chr18:14775044
|
A | C | 114 | a0001c0037t0003g0191a0002c0002t0001g0098a0002c0002t0001g0107others(111): Show | 115 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1329+2816A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14775044 | ||||||
| chr18:14775083
|
T | C | 9 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(6): Show | 10 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1329+2855T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14775083 | ||||||
| chr18:14775093
|
C | T | 3 | a0001c0001t0002g0276a0001c0001t0003g0275a0001c0001t0003g0279 | 3 | HG01106.hp1 HG01109.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1329+2865C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14775093 | ||||||
| chr18:14775149
|
G | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1330-2836G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14775149 | ||||||
| chr18:14775351
|
A | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1330-2634A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14775351 | ||||||
| chr18:14775606
|
G | A | 1 | a0001c0063t0004g0297 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1330-2379G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14775606 | ||||||
| chr18:14775812
|
A | G | 9 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(6): Show | 10 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1330-2173A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14775812 | ||||||
| chr18:14775985
|
G | C | 1 | a0002c0002t0001g0137 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1330-2000G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14775985 | ||||||
| chr18:14776682
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1330-1303C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14776682 | ||||||
| chr18:14776683
|
G | A | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-1302G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14776683 | ||||||
| chr18:14776900
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1330-1085T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14776900 | ||||||
| chr18:14776934
|
G | C | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-1051G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14776934 | ||||||
| chr18:14777002
|
T | G | 3 | a0002c0002t0001g0098a0002c0002t0001g0170a0002c0004t0001g0013 | 3 | HG00621.hp2 NA18968.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1330-983T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777002 | ||||||
| chr18:14777201
|
A | G | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1330-784A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777201 | ||||||
| chr18:14777297
|
AT | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(76): Show | 82 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1330-686delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr18 | 14777297 | |||||
| chr18:14777301
|
T | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(76): Show | 82 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1330-684T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777301 | ||||||
| chr18:14777334
|
C | T | 1 | a0001c0001t0003g0281 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1330-651C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777334 | ||||||
| chr18:14777449
|
C | T | 2 | a0001c0003t0004g0303a0040c0033t0004g0304 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1330-536C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777449 | ||||||
| chr18:14777464
|
A | C | 1 | a0013c0017t0005g0101 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1330-521A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777464 | ||||||
| chr18:14777549
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1330-436G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777549 | ||||||
| chr18:14777615
|
TA | T | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-364delA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr18 | 14777615 | |||||
| chr18:14777646
|
T | C | 6 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(3): Show | 6 | HG02055.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-339T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777646 | ||||||
| chr18:14777713
|
G | A | 1 | a0002c0002t0001g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1330-272G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777713 | ||||||
| chr18:14777744
|
C | G | 11 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(8): Show | 12 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1330-241C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777744 | ||||||
| chr18:14777814
|
C | T | 11 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(8): Show | 12 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1330-171C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 9/43 | chr18 | 14777814 | ||||||
| chr18:14778171
|
T | G | 1 | a0001c0003t0009g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1420+96T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14778171 | ||||||
| chr18:14778285
|
A | G | 3 | a0002c0002t0001g0168a0002c0002t0001g0175a0002c0002t0001g0189 | 3 | HG00735.hp2 HG02523.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1420+210A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14778285 | ||||||
| chr18:14778302
|
A | C | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1420+227A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14778302 | ||||||
| chr18:14778425
|
A | G | 2 | a0001c0003t0009g0228a0001c0003t0009g0229 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1420+350A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14778425 | ||||||
| chr18:14778529
|
G | A | 1 | a0002c0004t0001g0013 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1420+454G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14778529 | ||||||
| chr18:14778707
|
T | C | 2 | a0001c0001t0002g0041a0001c0001t0002g0051 | 2 | HG00423.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1420+632T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14778707 | ||||||
| chr18:14778738
|
A | AT | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1420+668dupT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | INFO_REALIGN_3_PRIME | chr18 | 14778738 | |||||
| chr18:14778777
|
C | T | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1420+702C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14778777 | ||||||
| chr18:14778909
|
T | C | 114 | a0001c0037t0003g0191a0002c0002t0001g0098a0002c0002t0001g0107others(111): Show | 115 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1420+834T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14778909 | ||||||
| chr18:14778945
|
T | C | 2 | a0006c0008t0001g0163a0006c0008t0001g0171 | 2 | HG01952.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1420+870T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14778945 | ||||||
| chr18:14779168
|
A | T | 1 | a0002c0002t0001g0167 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1421-792A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14779168 | ||||||
| chr18:14779281
|
A | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1421-679A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14779281 | ||||||
| chr18:14779401
|
C | T | 2 | a0002c0002t0001g0181a0002c0002t0001g0182 | 2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1421-559C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14779401 | ||||||
| chr18:14779485
|
A | G | 1 | a0020c0040t0001g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1421-475A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14779485 | ||||||
| chr18:14779653
|
T | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1421-307T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14779653 | ||||||
| chr18:14779788
|
T | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(77): Show | 80 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1421-172T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 10/43 | chr18 | 14779788 | ||||||
| chr18:14780083
|
G | A | 113 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(110): Show | 114 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1482+62G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | chr18 | 14780083 | ||||||
| chr18:14780288
|
A | T | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+267A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | chr18 | 14780288 | ||||||
| chr18:14780445
|
CA | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(20): Show | 26 | HG00544.hp2 HG00642.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1482+434delA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr18 | 14780445 | |||||
| chr18:14780498
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1482+477G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | chr18 | 14780498 | ||||||
| chr18:14780539
|
G | A | 1 | a0042c0052t0001g0079 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1482+518G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | chr18 | 14780539 | ||||||
| chr18:14780622
|
A | G | 1 | a0002c0002t0001g0212 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1482+601A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | chr18 | 14780622 | ||||||
| chr18:14780650
|
A | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482+629A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | chr18 | 14780650 | ||||||
| chr18:14781190
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1482+1169A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | chr18 | 14781190 | ||||||
| chr18:14781205
|
GCAGA | G | 7 | a0003c0006t0001g0003a0003c0006t0001g0237a0003c0006t0001g0240others(4): Show | 8 | HG02055.hp1 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482+1187_1482+119 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr18 | 14781205 | |||||
| chr18:14781288
|
C | CT | 28 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 28 | HG00621.hp2 HG01175.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1483-1215dupT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr18 | 14781288 | |||||
| chr18:14781288
|
C | CTT | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(121): Show | 127 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1483-1216_1483-121 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr18 | 14781288 | |||||
| chr18:14781288
|
C | CTTT | 26 | a0001c0001t0001g0011a0001c0001t0001g0260a0001c0001t0002g0018others(23): Show | 26 | HG00423.hp1 HG00609.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1483-1217_1483-121 others(7): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr18 | 14781288 | |||||
| chr18:14781288
|
CT | C | 7 | a0002c0002t0001g0138a0002c0002t0001g0189a0009c0013t0005g0100others(4): Show | 7 | HG02647.hp1 HG03098.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-1215delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr18 | 14781288 | |||||
| chr18:14781741
|
C | T | 1 | a0042c0052t0001g0079 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1483-786C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | chr18 | 14781741 | ||||||
| chr18:14782197
|
C | T | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1483-330C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 11/43 | chr18 | 14782197 | ||||||
| chr18:14782666
|
C | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+52C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14782666 | ||||||
| chr18:14782928
|
T | C | 6 | a0005c0005t0001g0302a0005c0005t0006g0232a0005c0005t0006g0233others(3): Show | 6 | HG02280.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1570+314T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14782928 | ||||||
| chr18:14782997
|
A | T | 2 | a0009c0013t0005g0104a0009c0013t0005g0105 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1570+383A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14782997 | ||||||
| chr18:14783021
|
T | C | 1 | a0002c0002t0001g0164 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1570+407T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14783021 | ||||||
| chr18:14783073
|
T | C | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+459T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14783073 | ||||||
| chr18:14783153
|
C | T | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1570+539C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14783153 | ||||||
| chr18:14783155
|
A | G | 1 | a0011c0014t0001g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1570+541A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14783155 | ||||||
| chr18:14783542
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1571-794C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14783542 | ||||||
| chr18:14783600
|
A | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1571-736A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14783600 | ||||||
| chr18:14783642
|
A | G | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1571-694A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14783642 | ||||||
| chr18:14783748
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0039 | 3 | NA19007.hp1 NA19010.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1571-588T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14783748 | ||||||
| chr18:14783763
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 162 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1571-573A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14783763 | ||||||
| chr18:14783896
|
A | T | 1 | a0006c0008t0001g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1571-440A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14783896 | ||||||
| chr18:14784055
|
G | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-281G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14784055 | ||||||
| chr18:14784280
|
C | T | 2 | a0002c0002t0001g0109a0002c0002t0001g0156 | 2 | NA18994.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1571-56C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14784280 | ||||||
| chr18:14784281
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1571-55G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 12/43 | chr18 | 14784281 | ||||||
| chr18:14784723
|
T | TA | 15 | a0001c0001t0002g0033a0001c0001t0002g0060a0001c0001t0002g0061others(12): Show | 15 | HG00323.hp2 HG01074.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1672+195dupA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr18 | 14784723 | |||||
| chr18:14784724
|
A | T | 5 | a0002c0002t0001g0146a0009c0013t0005g0100a0009c0013t0005g0104others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1672+189A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14784724 | ||||||
| chr18:14784769
|
G | A | 1 | a0001c0037t0003g0191 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1672+234G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14784769 | ||||||
| chr18:14784843
|
T | TC | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(304): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.1672+308_1672+309i others(3): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14784843 | ||||||
| chr18:14784877
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1672+342C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14784877 | ||||||
| chr18:14784898
|
T | A | 1 | a0002c0002t0001g0198 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1672+363T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14784898 | ||||||
| chr18:14784916
|
C | G | 1 | a0001c0063t0004g0297 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1672+381C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14784916 | ||||||
| chr18:14784976
|
C | A | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1672+441C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14784976 | ||||||
| chr18:14785096
|
T | A | 1 | a0001c0001t0002g0016 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1672+561T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14785096 | ||||||
| chr18:14785347
|
T | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1672+812T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14785347 | ||||||
| chr18:14785363
|
A | C | 1 | a0001c0001t0002g0045 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1672+828A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14785363 | ||||||
| chr18:14785364
|
C | A | 1 | a0001c0001t0002g0045 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1672+829C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14785364 | ||||||
| chr18:14785491
|
C | T | 1 | a0001c0001t0002g0020 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1672+956C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14785491 | ||||||
| chr18:14785809
|
C | T | 1 | a0002c0002t0001g0136 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1673-1230C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14785809 | ||||||
| chr18:14785875
|
A | G | 8 | a0001c0001t0002g0065a0001c0003t0002g0151a0001c0003t0002g0155others(5): Show | 8 | HG02027.hp2 HG02056.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1673-1164A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14785875 | ||||||
| chr18:14785907
|
G | T | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1673-1132G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14785907 | ||||||
| chr18:14785911
|
G | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1673-1128G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14785911 | ||||||
| chr18:14785994
|
C | A | 1 | a0002c0004t0001g0021 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1673-1045C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14785994 | ||||||
| chr18:14786032
|
G | A | 2 | a0001c0001t0001g0008a0002c0002t0001g0137 | 2 | HG01167.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1673-1007G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14786032 | ||||||
| chr18:14786044
|
C | CA | 9 | a0001c0003t0002g0123a0002c0002t0001g0176a0003c0019t0001g0090others(6): Show | 9 | HG01123.hp1 HG01175.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1673-968dupA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr18 | 14786044 | |||||
| chr18:14786044
|
C | CAA | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1673-969_1673-968d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr18 | 14786044 | |||||
| chr18:14786044
|
CA | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(203): Show | 210 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.1673-968delA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr18 | 14786044 | |||||
| chr18:14786044
|
CAA | C | 25 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0001g0127others(22): Show | 25 | HG00099.hp2 HG01069.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1673-969_1673-968d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr18 | 14786044 | |||||
| chr18:14786149
|
C | T | 2 | a0001c0003t0009g0228a0001c0003t0009g0229 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1673-890C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14786149 | ||||||
| chr18:14786193
|
A | T | 1 | a0011c0014t0001g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1673-846A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14786193 | ||||||
| chr18:14786297
|
C | G | 1 | a0001c0060t0002g0077 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1673-742C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14786297 | ||||||
| chr18:14786307
|
A | C | 1 | a0018c0032t0002g0213 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1673-732A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14786307 | ||||||
| chr18:14786381
|
G | A | 1 | a0002c0002t0001g0172 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1673-658G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14786381 | ||||||
| chr18:14786525
|
G | A | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1673-514G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14786525 | ||||||
| chr18:14786808
|
G | C | 1 | a0001c0001t0002g0065 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1673-231G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14786808 | ||||||
| chr18:14786986
|
A | G | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1673-53A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 14/43 | chr18 | 14786986 | ||||||
| chr18:14787273
|
C | T | 1 | a0002c0004t0001g0254 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1734+173C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14787273 | ||||||
| chr18:14787451
|
G | C | 112 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(109): Show | 113 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1734+351G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14787451 | ||||||
| chr18:14787669
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1734+569G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14787669 | ||||||
| chr18:14787725
|
G | C | 1 | a0009c0013t0005g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1734+625G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14787725 | ||||||
| chr18:14787801
|
C | T | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1734+701C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14787801 | ||||||
| chr18:14788124
|
G | A | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1734+1024G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788124 | ||||||
| chr18:14788253
|
G | C | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734+1153G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788253 | ||||||
| chr18:14788259
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1734+1159T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788259 | ||||||
| chr18:14788440
|
A | T | 2 | a0002c0002t0001g0181a0002c0002t0001g0182 | 2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1734+1340A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788440 | ||||||
| chr18:14788448
|
T | G | 2 | a0002c0002t0001g0181a0002c0002t0001g0182 | 2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1734+1348T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788448 | ||||||
| chr18:14788466
|
T | C | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(304): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.1734+1366T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788466 | ||||||
| chr18:14788501
|
G | A | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1734+1401G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788501 | ||||||
| chr18:14788750
|
A | T | 112 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(109): Show | 113 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1734+1650A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788750 | ||||||
| chr18:14788786
|
G | A | 1 | a0004c0007t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1734+1686G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788786 | ||||||
| chr18:14788856
|
T | C | 2 | a0002c0002t0001g0209a0002c0004t0001g0284 | 2 | HG02165.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1734+1756T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788856 | ||||||
| chr18:14788886
|
T | G | 65 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1734+1786T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788886 | ||||||
| chr18:14788944
|
G | A | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1734+1844G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788944 | ||||||
| chr18:14788986
|
G | A | 1 | a0027c0028t0001g0165 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1734+1886G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14788986 | ||||||
| chr18:14789004
|
C | G | 1 | a0002c0002t0001g0136 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1734+1904C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789004 | ||||||
| chr18:14789018
|
A | C | 9 | a0001c0003t0004g0298a0004c0007t0001g0005a0004c0007t0001g0299others(6): Show | 10 | HG02055.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1734+1918A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789018 | ||||||
| chr18:14789054
|
C | G | 11 | a0005c0005t0001g0302a0005c0005t0006g0232a0005c0005t0006g0233others(8): Show | 11 | HG01891.hp2 HG01952.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1734+1954C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789054 | ||||||
| chr18:14789078
|
A | C | 1 | a0023c0043t0001g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1734+1978A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789078 | ||||||
| chr18:14789117
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1734+2017A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789117 | ||||||
| chr18:14789144
|
A | G | 65 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1734+2044A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789144 | ||||||
| chr18:14789275
|
A | C | 6 | a0001c0001t0001g0253a0001c0001t0001g0259a0001c0001t0001g0260others(3): Show | 6 | HG02895.hp1 HG02965.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1735-2126A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789275 | ||||||
| chr18:14789375
|
G | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1735-2026G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789375 | ||||||
| chr18:14789415
|
T | C | 2 | a0001c0003t0001g0125a0001c0003t0001g0126 | 2 | HG01192.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1735-1986T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789415 | ||||||
| chr18:14789420
|
T | A | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-1981T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789420 | ||||||
| chr18:14789565
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1735-1836G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789565 | ||||||
| chr18:14789618
|
G | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1735-1783G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789618 | ||||||
| chr18:14789648
|
A | C | 1 | a0039c0056t0001g0257 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1735-1753A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789648 | ||||||
| chr18:14789677
|
G | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1735-1724G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789677 | ||||||
| chr18:14789699
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1735-1702C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789699 | ||||||
| chr18:14789708
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1735-1693C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789708 | ||||||
| chr18:14789709
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1735-1692A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789709 | ||||||
| chr18:14789710
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1735-1691C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789710 | ||||||
| chr18:14789712
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1735-1689A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789712 | ||||||
| chr18:14789725
|
G | A | 1 | a0027c0028t0001g0165 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1735-1676G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789725 | ||||||
| chr18:14789748
|
A | G | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1735-1653A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789748 | ||||||
| chr18:14789775
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(157): Show | 163 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1735-1626G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789775 | ||||||
| chr18:14789861
|
CT | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1735-1538delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | INFO_REALIGN_3_PRIME | chr18 | 14789861 | |||||
| chr18:14789914
|
C | G | 1 | a0002c0002t0001g0137 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1735-1487C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789914 | ||||||
| chr18:14789955
|
G | T | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1735-1446G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789955 | ||||||
| chr18:14789956
|
C | T | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1735-1445C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14789956 | ||||||
| chr18:14790375
|
C | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 162 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1735-1026C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790375 | ||||||
| chr18:14790532
|
T | A | 112 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(109): Show | 113 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1735-869T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790532 | ||||||
| chr18:14790558
|
C | T | 1 | a0002c0004t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1735-843C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790558 | ||||||
| chr18:14790601
|
G | C | 1 | a0001c0003t0002g0113 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1735-800G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790601 | ||||||
| chr18:14790602
|
G | A | 1 | a0001c0003t0002g0113 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1735-799G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790602 | ||||||
| chr18:14790697
|
G | A | 1 | a0001c0003t0004g0303 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1735-704G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790697 | ||||||
| chr18:14790784
|
C | T | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1735-617C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790784 | ||||||
| chr18:14790786
|
G | T | 1 | a0001c0001t0002g0020 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1735-615G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790786 | ||||||
| chr18:14790838
|
G | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-563G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790838 | ||||||
| chr18:14790856
|
T | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(157): Show | 163 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1735-545T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790856 | ||||||
| chr18:14790859
|
T | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(157): Show | 163 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1735-542T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790859 | ||||||
| chr18:14790870
|
T | C | 1 | a0001c0003t0004g0298 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1735-531T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790870 | ||||||
| chr18:14790957
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(157): Show | 163 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1735-444G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790957 | ||||||
| chr18:14790982
|
A | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-419A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790982 | ||||||
| chr18:14790983
|
T | C | 3 | a0002c0002t0001g0098a0002c0002t0001g0170a0002c0004t0001g0013 | 3 | HG00621.hp2 NA18968.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1735-418T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14790983 | ||||||
| chr18:14791032
|
T | G | 1 | a0001c0001t0002g0057 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1735-369T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791032 | ||||||
| chr18:14791079
|
C | G | 11 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(8): Show | 11 | HG01891.hp1 HG02258.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1735-322C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791079 | ||||||
| chr18:14791080
|
G | A | 1 | a0002c0002t0001g0149 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1735-321G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791080 | ||||||
| chr18:14791101
|
A | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1735-300A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791101 | ||||||
| chr18:14791111
|
TA | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-289delA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791111 | ||||||
| chr18:14791114
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-287T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791114 | ||||||
| chr18:14791118
|
G | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-283G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791118 | ||||||
| chr18:14791119
|
G | GACTTTTC others(6880): Show |
3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-282_1735-281i others(6889): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791119 | ||||||
| chr18:14791124
|
G | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-277G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791124 | ||||||
| chr18:14791126
|
G | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-275G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791126 | ||||||
| chr18:14791133
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-268T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791133 | ||||||
| chr18:14791135
|
G | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-266G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791135 | ||||||
| chr18:14791138
|
G | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-263G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791138 | ||||||
| chr18:14791140
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-261A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791140 | ||||||
| chr18:14791141
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-260T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791141 | ||||||
| chr18:14791143
|
T | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-258T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791143 | ||||||
| chr18:14791144
|
A | ACTGCTTC others(4): Show |
3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-257_1735-256i others(13): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791144 | ||||||
| chr18:14791146
|
C | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-255C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791146 | ||||||
| chr18:14791147
|
C | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-254C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791147 | ||||||
| chr18:14791149
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-252T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791149 | ||||||
| chr18:14791154
|
T | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-247T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791154 | ||||||
| chr18:14791157
|
AG | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-243delG | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791157 | ||||||
| chr18:14791165
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-236T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791165 | ||||||
| chr18:14791166
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-235A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791166 | ||||||
| chr18:14791167
|
G | GC | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-234_1735-233i others(3): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791167 | ||||||
| chr18:14791170
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-231T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791170 | ||||||
| chr18:14791175
|
G | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-226G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791175 | ||||||
| chr18:14791176
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-225T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791176 | ||||||
| chr18:14791178
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-223T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791178 | ||||||
| chr18:14791180
|
G | GC | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-221_1735-220i others(3): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791180 | ||||||
| chr18:14791181
|
A | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-220A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791181 | ||||||
| chr18:14791186
|
T | TG | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-215_1735-214i others(3): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791186 | ||||||
| chr18:14791187
|
T | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-214T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791187 | ||||||
| chr18:14791193
|
T | TGTAAAAA others(623): Show |
3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-208_1735-207i others(632): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791193 | ||||||
| chr18:14791201
|
G | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-200G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791201 | ||||||
| chr18:14791202
|
A | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-199A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791202 | ||||||
| chr18:14791203
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-198T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791203 | ||||||
| chr18:14791204
|
G | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-197G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791204 | ||||||
| chr18:14791208
|
G | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-193G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791208 | ||||||
| chr18:14791212
|
G | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-189G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791212 | ||||||
| chr18:14791214
|
A | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-187A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791214 | ||||||
| chr18:14791216
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-185T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791216 | ||||||
| chr18:14791218
|
C | CAGCATAA others(374): Show |
3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-183_1735-182i others(383): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791218 | ||||||
| chr18:14791223
|
G | GA | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-178_1735-177i others(3): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791223 | ||||||
| chr18:14791226
|
T | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-175T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791226 | ||||||
| chr18:14791229
|
A | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-172A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791229 | ||||||
| chr18:14791230
|
T | TA | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-171_1735-170i others(3): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791230 | ||||||
| chr18:14791231
|
G | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-170G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791231 | ||||||
| chr18:14791235
|
A | AGGT | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-166_1735-165i others(5): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791235 | ||||||
| chr18:14791237
|
T | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(77): Show | 83 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1735-164T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791237 | ||||||
| chr18:14791245
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-156A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791245 | ||||||
| chr18:14791255
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-146A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791255 | ||||||
| chr18:14791256
|
T | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-145T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791256 | ||||||
| chr18:14791261
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-140T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791261 | ||||||
| chr18:14791263
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-138T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791263 | ||||||
| chr18:14791266
|
G | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-135G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791266 | ||||||
| chr18:14791270
|
G | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-131G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791270 | ||||||
| chr18:14791271
|
T | C | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-130T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791271 | ||||||
| chr18:14791272
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-129A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791272 | ||||||
| chr18:14791288
|
G | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-113G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791288 | ||||||
| chr18:14791289
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-112T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791289 | ||||||
| chr18:14791293
|
C | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-108C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791293 | ||||||
| chr18:14791297
|
C | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-104C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791297 | ||||||
| chr18:14791305
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-96T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791305 | ||||||
| chr18:14791316
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-85A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791316 | ||||||
| chr18:14791325
|
C | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-76C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791325 | ||||||
| chr18:14791328
|
G | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-73G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791328 | ||||||
| chr18:14791333
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-68A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791333 | ||||||
| chr18:14791336
|
A | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-65A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791336 | ||||||
| chr18:14791355
|
C | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-46C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791355 | ||||||
| chr18:14791357
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-44A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791357 | ||||||
| chr18:14791364
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-37T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791364 | ||||||
| chr18:14791366
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1735-35T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 15/43 | chr18 | 14791366 | ||||||
| chr18:14791503
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+12T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791503 | ||||||
| chr18:14791509
|
A | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+18A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791509 | ||||||
| chr18:14791532
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+41A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791532 | ||||||
| chr18:14791536
|
A | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+45A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791536 | ||||||
| chr18:14791540
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+49A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791540 | ||||||
| chr18:14791553
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+62A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791553 | ||||||
| chr18:14791562
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+71T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791562 | ||||||
| chr18:14791570
|
A | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+79A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791570 | ||||||
| chr18:14791589
|
T | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+98T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791589 | ||||||
| chr18:14791601
|
C | T | 5 | a0011c0014t0001g0264a0011c0014t0001g0265a0012c0012t0002g0108others(2): Show | 5 | HG02135.hp2 NA18747.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+110C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791601 | ||||||
| chr18:14791602
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+111A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791602 | ||||||
| chr18:14791621
|
C | T | 7 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(4): Show | 7 | HG02135.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+130C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791621 | ||||||
| chr18:14791646
|
G | T | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+155G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791646 | ||||||
| chr18:14791654
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+163T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791654 | ||||||
| chr18:14791656
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+165A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791656 | ||||||
| chr18:14791661
|
G | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+170G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791661 | ||||||
| chr18:14791664
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+173T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791664 | ||||||
| chr18:14791667
|
T | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+176T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791667 | ||||||
| chr18:14791672
|
G | A | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1825+181G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791672 | ||||||
| chr18:14791678
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+187A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791678 | ||||||
| chr18:14791756
|
A | C | 1 | a0029c0024t0001g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1825+265A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791756 | ||||||
| chr18:14791756
|
A | T | 4 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0084others(1): Show | 4 | HG02683.hp1 HG03491.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+265A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791756 | ||||||
| chr18:14791804
|
C | A | 1 | a0001c0001t0002g0071 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1825+313C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791804 | ||||||
| chr18:14791873
|
T | C | 9 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(6): Show | 9 | HG02135.hp2 HG02258.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1825+382T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791873 | ||||||
| chr18:14791877
|
C | T | 4 | a0001c0001t0003g0243a0012c0012t0002g0108a0012c0012t0002g0153others(1): Show | 4 | HG02135.hp2 HG02145.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1825+386C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791877 | ||||||
| chr18:14791901
|
G | A | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+410G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791901 | ||||||
| chr18:14791915
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+424T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791915 | ||||||
| chr18:14791917
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1825+426A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791917 | ||||||
| chr18:14791925
|
A | T | 3 | a0006c0008t0001g0190a0006c0008t0001g0219a0013c0017t0005g0101 | 3 | HG01891.hp2 HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1825+434A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791925 | ||||||
| chr18:14791933
|
G | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(165): Show | 172 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.1825+442G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791933 | ||||||
| chr18:14791942
|
A | G | 1 | a0044c0064t0001g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1825+451A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791942 | ||||||
| chr18:14791993
|
G | A | 3 | a0001c0001t0003g0286a0016c0031t0003g0124a0016c0050t0003g0059 | 3 | HG00609.hp1 HG02027.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1825+502G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14791993 | ||||||
| chr18:14792061
|
T | C | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+570T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792061 | ||||||
| chr18:14792106
|
A | G | 3 | a0012c0012t0002g0108a0012c0012t0002g0153a0012c0012t0002g0154 | 3 | HG02135.hp2 NA18747.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1825+615A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792106 | ||||||
| chr18:14792145
|
T | C | 1 | a0001c0001t0003g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1825+654T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792145 | ||||||
| chr18:14792408
|
G | A | 2 | a0002c0002t0001g0170a0002c0004t0001g0013 | 2 | HG00621.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1825+917G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792408 | ||||||
| chr18:14792509
|
T | A | 113 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(110): Show | 114 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1825+1018T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792509 | ||||||
| chr18:14792594
|
C | T | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1825+1103C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792594 | ||||||
| chr18:14792615
|
C | T | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(296): Show | 304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.1825+1124C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792615 | ||||||
| chr18:14792633
|
T | C | 6 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1825+1142T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792633 | ||||||
| chr18:14792687
|
C | A | 3 | a0001c0001t0003g0286a0016c0031t0003g0124a0016c0050t0003g0059 | 3 | HG00609.hp1 HG02027.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1825+1196C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792687 | ||||||
| chr18:14792688
|
C | T | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1825+1197C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792688 | ||||||
| chr18:14792729
|
A | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+1238A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792729 | ||||||
| chr18:14792729
|
AAT | A | 139 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(136): Show | 142 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1825+1257_1825+125 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | INFO_REALIGN_3_PRIME | chr18 | 14792729 | |||||
| chr18:14792729
|
AATAT | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(158): Show | 164 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1825+1255_1825+125 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | INFO_REALIGN_3_PRIME | chr18 | 14792729 | |||||
| chr18:14792924
|
C | A | 1 | a0001c0003t0002g0123 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1825+1433C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792924 | ||||||
| chr18:14792924
|
C | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+1433C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792924 | ||||||
| chr18:14792986
|
T | C | 5 | a0001c0001t0001g0253a0001c0001t0001g0259a0001c0001t0001g0260others(2): Show | 5 | HG02895.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+1495T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14792986 | ||||||
| chr18:14793078
|
G | A | 2 | a0002c0002t0001g0140a0002c0004t0001g0037 | 2 | NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1825+1587G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14793078 | ||||||
| chr18:14793288
|
A | C | 1 | a0001c0003t0002g0123 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1825+1797A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14793288 | ||||||
| chr18:14793344
|
G | C | 112 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(109): Show | 113 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1825+1853G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14793344 | ||||||
| chr18:14793401
|
T | C | 1 | a0002c0002t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1825+1910T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14793401 | ||||||
| chr18:14793471
|
A | G | 11 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(8): Show | 11 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1825+1980A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14793471 | ||||||
| chr18:14793495
|
A | C | 1 | a0001c0001t0002g0017 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1825+2004A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14793495 | ||||||
| chr18:14793843
|
G | A | 8 | a0001c0001t0003g0251a0001c0001t0003g0282a0001c0001t0003g0283others(5): Show | 8 | HG00609.hp1 HG02027.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1825+2352G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14793843 | ||||||
| chr18:14793888
|
C | T | 1 | a0035c0054t0001g0258 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1826-2333C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14793888 | ||||||
| chr18:14793896
|
G | GA | 6 | a0008c0010t0001g0262a0008c0010t0008g0006a0008c0010t0008g0007others(3): Show | 6 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-2313dupA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | INFO_REALIGN_3_PRIME | chr18 | 14793896 | |||||
| chr18:14793896
|
GA | G | 18 | a0001c0001t0002g0045a0001c0001t0002g0061a0001c0003t0001g0186others(15): Show | 18 | HG00642.hp2 HG01515.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1826-2313delA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | INFO_REALIGN_3_PRIME | chr18 | 14793896 | |||||
| chr18:14794045
|
A | G | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-2176A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794045 | ||||||
| chr18:14794296
|
A | C | 4 | a0001c0003t0002g0112a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG01074.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-1925A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794296 | ||||||
| chr18:14794644
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1826-1577C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794644 | ||||||
| chr18:14794712
|
A | G | 1 | a0002c0002t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1826-1509A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794712 | ||||||
| chr18:14794737
|
T | A | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826-1484T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794737 | ||||||
| chr18:14794786
|
G | T | 1 | a0040c0033t0004g0304 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1826-1435G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794786 | ||||||
| chr18:14794821
|
A | G | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-1400A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794821 | ||||||
| chr18:14794933
|
G | T | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1826-1288G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794933 | ||||||
| chr18:14794949
|
T | G | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(304): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.1826-1272T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794949 | ||||||
| chr18:14794965
|
T | C | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-1256T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794965 | ||||||
| chr18:14794969
|
T | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826-1252T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14794969 | ||||||
| chr18:14795104
|
C | G | 1 | a0002c0002t0001g0180 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1826-1117C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795104 | ||||||
| chr18:14795106
|
A | C | 1 | a0041c0034t0004g0300 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1826-1115A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795106 | ||||||
| chr18:14795114
|
T | A | 1 | a0001c0001t0003g0269 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1826-1107T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795114 | ||||||
| chr18:14795116
|
C | T | 1 | a0001c0015t0001g0064 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1826-1105C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795116 | ||||||
| chr18:14795170
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1826-1051C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795170 | ||||||
| chr18:14795171
|
A | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826-1050A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795171 | ||||||
| chr18:14795200
|
G | A | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1826-1021G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795200 | ||||||
| chr18:14795228
|
G | A | 1 | a0001c0011t0003g0280 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1826-993G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795228 | ||||||
| chr18:14795485
|
T | C | 23 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(20): Show | 24 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1826-736T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795485 | ||||||
| chr18:14795487
|
C | G | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-734C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795487 | ||||||
| chr18:14795498
|
G | A | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826-723G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795498 | ||||||
| chr18:14795555
|
T | C | 1 | a0003c0006t0001g0237 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1826-666T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795555 | ||||||
| chr18:14795654
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-567G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795654 | ||||||
| chr18:14795724
|
C | G | 1 | a0026c0029t0001g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1826-497C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795724 | ||||||
| chr18:14795798
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1826-423C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795798 | ||||||
| chr18:14795853
|
A | AT | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-354dupT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | INFO_REALIGN_3_PRIME | chr18 | 14795853 | |||||
| chr18:14795853
|
AT | A | 7 | a0001c0001t0001g0008a0001c0001t0003g0281a0001c0003t0002g0097others(4): Show | 7 | HG01167.hp1 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-354delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | INFO_REALIGN_3_PRIME | chr18 | 14795853 | |||||
| chr18:14795870
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1826-351C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795870 | ||||||
| chr18:14795956
|
A | C | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-265A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795956 | ||||||
| chr18:14795993
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1826-228A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14795993 | ||||||
| chr18:14796057
|
G | A | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-164G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14796057 | ||||||
| chr18:14796081
|
G | A | 65 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1826-140G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14796081 | ||||||
| chr18:14796215
|
G | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
splice_region_variant&intron_variant | LOW | c.1826-6G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 16/43 | chr18 | 14796215 | ||||||
| chr18:14796335
|
C | A | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1855-8C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 17/43 | chr18 | 14796335 | ||||||
| chr18:14796444
|
G | T | 112 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(109): Show | 113 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1927+29G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796444 | ||||||
| chr18:14796476
|
G | A | 1 | a0008c0010t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1927+61G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796476 | ||||||
| chr18:14796549
|
T | G | 1 | a0002c0002t0001g0137 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1927+134T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796549 | ||||||
| chr18:14796617
|
T | A | 1 | a0001c0001t0002g0080 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1927+202T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796617 | ||||||
| chr18:14796653
|
A | G | 1 | a0002c0002t0001g0180 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1927+238A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796653 | ||||||
| chr18:14796697
|
G | A | 1 | a0001c0063t0004g0297 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1927+282G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796697 | ||||||
| chr18:14796714
|
C | G | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1927+299C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796714 | ||||||
| chr18:14796870
|
C | A | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1927+455C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796870 | ||||||
| chr18:14796875
|
T | G | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1927+460T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796875 | ||||||
| chr18:14796897
|
A | C | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1927+482A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796897 | ||||||
| chr18:14796975
|
C | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1927+560C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14796975 | ||||||
| chr18:14797028
|
C | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1927+613C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797028 | ||||||
| chr18:14797048
|
A | G | 1 | a0028c0025t0001g0202 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1928-613A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797048 | ||||||
| chr18:14797202
|
A | T | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1928-459A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797202 | ||||||
| chr18:14797211
|
C | T | 1 | a0001c0001t0003g0275 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1928-450C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797211 | ||||||
| chr18:14797306
|
C | T | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1928-355C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797306 | ||||||
| chr18:14797351
|
G | T | 3 | a0001c0003t0001g0125a0001c0003t0001g0126a0001c0003t0001g0127 | 3 | HG01069.hp2 HG01192.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1928-310G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797351 | ||||||
| chr18:14797399
|
T | A | 1 | a0001c0003t0002g0188 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1928-262T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797399 | ||||||
| chr18:14797433
|
T | C | 3 | a0001c0001t0002g0033a0001c0001t0002g0060a0001c0001t0002g0061 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1928-228T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797433 | ||||||
| chr18:14797473
|
A | G | 12 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(9): Show | 13 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1928-188A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797473 | ||||||
| chr18:14797477
|
T | A | 1 | a0002c0002t0001g0197 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1928-184T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797477 | ||||||
| chr18:14797571
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1928-90G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797571 | ||||||
| chr18:14797594
|
G | A | 1 | a0002c0004t0001g0266 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1928-67G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 18/43 | chr18 | 14797594 | ||||||
| chr18:14797728
|
A | G | 1 | a0020c0040t0001g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1956+39A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 19/43 | chr18 | 14797728 | ||||||
| chr18:14797741
|
G | A | 2 | a0004c0022t0001g0301a0004c0045t0010g0089 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1957-41G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 19/43 | chr18 | 14797741 | ||||||
| chr18:14797902
|
T | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2029+48T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14797902 | ||||||
| chr18:14797914
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.2029+60C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14797914 | ||||||
| chr18:14797915
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.2029+61A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14797915 | ||||||
| chr18:14797919
|
G | T | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2029+65G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14797919 | ||||||
| chr18:14797964
|
A | C | 1 | a0002c0002t0001g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2029+110A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14797964 | ||||||
| chr18:14798066
|
A | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2029+212A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798066 | ||||||
| chr18:14798094
|
G | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2029+240G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798094 | ||||||
| chr18:14798096
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2029+242G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798096 | ||||||
| chr18:14798137
|
T | G | 1 | a0001c0001t0002g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2029+283T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798137 | ||||||
| chr18:14798183
|
C | T | 1 | a0002c0002t0001g0231 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2029+329C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798183 | ||||||
| chr18:14798197
|
G | A | 1 | a0002c0002t0001g0180 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2029+343G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798197 | ||||||
| chr18:14798287
|
A | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(157): Show | 163 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2029+433A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798287 | ||||||
| chr18:14798327
|
TTAAC | T | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2029+478_2029+481d others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | INFO_REALIGN_3_PRIME | chr18 | 14798327 | |||||
| chr18:14798467
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(183): Show | 190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.2029+613T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798467 | ||||||
| chr18:14798495
|
C | G | 65 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2030-606C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798495 | ||||||
| chr18:14798582
|
G | GC | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2030-518dupC | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | INFO_REALIGN_3_PRIME | chr18 | 14798582 | |||||
| chr18:14798593
|
C | T | 2 | a0004c0022t0001g0301a0004c0045t0010g0089 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2030-508C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798593 | ||||||
| chr18:14798610
|
G | A | 1 | a0001c0001t0003g0281 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2030-491G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798610 | ||||||
| chr18:14798686
|
C | G | 1 | a0001c0001t0002g0051 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2030-415C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798686 | ||||||
| chr18:14798736
|
G | C | 2 | a0001c0036t0002g0192a0001c0059t0002g0050 | 2 | HG00099.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2030-365G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798736 | ||||||
| chr18:14798743
|
T | G | 113 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(110): Show | 114 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.2030-358T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798743 | ||||||
| chr18:14798755
|
G | T | 1 | a0002c0002t0001g0215 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2030-346G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798755 | ||||||
| chr18:14798758
|
G | T | 1 | a0002c0002t0001g0133 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2030-343G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798758 | ||||||
| chr18:14798790
|
T | A | 23 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(20): Show | 24 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.2030-311T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798790 | ||||||
| chr18:14798842
|
T | C | 2 | a0002c0002t0001g0225a0002c0002t0001g0248 | 2 | NA19075.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.2030-259T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798842 | ||||||
| chr18:14798861
|
A | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2030-240A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798861 | ||||||
| chr18:14798911
|
C | T | 23 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(20): Show | 24 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.2030-190C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798911 | ||||||
| chr18:14798932
|
C | T | 1 | a0002c0002t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2030-169C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798932 | ||||||
| chr18:14798970
|
C | G | 1 | a0001c0003t0002g0196 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2030-131C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798970 | ||||||
| chr18:14798996
|
A | G | 1 | a0002c0002t0001g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2030-105A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 20/43 | chr18 | 14798996 | ||||||
| chr18:14799143
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2058+14T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 21/43 | chr18 | 14799143 | ||||||
| chr18:14799163
|
C | T | 6 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2058+34C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 21/43 | chr18 | 14799163 | ||||||
| chr18:14799348
|
G | A | 1 | a0015c0048t0001g0096 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2131+53G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14799348 | ||||||
| chr18:14799464
|
C | T | 2 | a0002c0004t0001g0254a0002c0004t0001g0288 | 2 | HG00738.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2131+169C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14799464 | ||||||
| chr18:14799530
|
T | C | 112 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(109): Show | 113 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.2131+235T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14799530 | ||||||
| chr18:14799544
|
C | T | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2131+249C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14799544 | ||||||
| chr18:14799568
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(157): Show | 163 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2131+273C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14799568 | ||||||
| chr18:14799670
|
G | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2131+375G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14799670 | ||||||
| chr18:14799679
|
T | C | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2131+384T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14799679 | ||||||
| chr18:14799712
|
A | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(157): Show | 163 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2131+417A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14799712 | ||||||
| chr18:14799744
|
A | AGT | 11 | a0001c0001t0002g0033a0001c0001t0002g0060a0001c0001t0002g0061others(8): Show | 11 | HG00323.hp2 HG00735.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.2131+467_2131+468d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr18 | 14799744 | |||||
| chr18:14799823
|
G | A | 15 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(12): Show | 15 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2131+528G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14799823 | ||||||
| chr18:14800023
|
G | A | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2131+728G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800023 | ||||||
| chr18:14800094
|
T | C | 1 | a0003c0006t0008g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2131+799T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800094 | ||||||
| chr18:14800109
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2131+814G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800109 | ||||||
| chr18:14800145
|
T | C | 1 | a0001c0001t0002g0073 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2131+850T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800145 | ||||||
| chr18:14800150
|
T | C | 1 | a0002c0002t0001g0172 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2131+855T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800150 | ||||||
| chr18:14800232
|
G | GCAAA | 18 | a0001c0001t0002g0045a0004c0007t0001g0005a0004c0007t0001g0299others(15): Show | 19 | HG01243.hp1 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.2131+941_2131+944d others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr18 | 14800232 | |||||
| chr18:14800293
|
G | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(288): Show | 296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.2131+998G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800293 | ||||||
| chr18:14800318
|
T | A | 1 | a0011c0014t0001g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2131+1023T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800318 | ||||||
| chr18:14800363
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.2131+1068T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800363 | ||||||
| chr18:14800418
|
A | G | 17 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 17 | HG00621.hp1 HG02132.hp1 HG02735.hp1 others(14): Show |
intron_variant | MODIFIER | c.2131+1123A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800418 | ||||||
| chr18:14800420
|
G | C | 17 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 17 | HG00621.hp1 HG02132.hp1 HG02735.hp1 others(14): Show |
intron_variant | MODIFIER | c.2131+1125G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800420 | ||||||
| chr18:14800468
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(185): Show | 192 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.2131+1173A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800468 | ||||||
| chr18:14800473
|
T | C | 7 | a0001c0001t0002g0045a0002c0002t0001g0119a0002c0002t0001g0174others(4): Show | 7 | HG01069.hp1 HG01081.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.2131+1178T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800473 | ||||||
| chr18:14800483
|
C | A | 1 | a0012c0012t0002g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2131+1188C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800483 | ||||||
| chr18:14800541
|
A | G | 4 | a0001c0001t0002g0045a0013c0017t0001g0009a0021c0042t0005g0099others(1): Show | 4 | HG03453.hp2 HG03471.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.2131+1246A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800541 | ||||||
| chr18:14800545
|
C | T | 2 | a0001c0001t0002g0045a0037c0058t0002g0044 | 2 | NA19082.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2131+1250C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800545 | ||||||
| chr18:14800575
|
C | T | 9 | a0004c0007t0001g0299a0004c0007t0001g0309a0004c0007t0001g0310others(6): Show | 9 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2131+1280C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800575 | ||||||
| chr18:14800575
|
C | TGGCCTCC others(10875): Show |
1 | a0004c0007t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2131+1279_2131+128 others(10886): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800575 | ||||||
| chr18:14800605
|
T | A | 1 | a0001c0011t0003g0274 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2131+1310T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800605 | ||||||
| chr18:14800611
|
A | T | 112 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(109): Show | 113 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.2131+1316A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800611 | ||||||
| chr18:14800731
|
C | T | 3 | a0002c0002t0001g0119a0002c0002t0001g0174a0002c0002t0001g0184 | 3 | HG01069.hp1 HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2131+1436C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800731 | ||||||
| chr18:14800877
|
G | A | 20 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(17): Show | 21 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.2132-1340G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14800877 | ||||||
| chr18:14801301
|
C | A | 2 | a0002c0002t0001g0225a0002c0002t0001g0248 | 2 | NA19075.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.2132-916C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14801301 | ||||||
| chr18:14801406
|
G | T | 1 | a0008c0010t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2132-811G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14801406 | ||||||
| chr18:14801481
|
CAT | C | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2132-735_2132-734d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14801481 | ||||||
| chr18:14801512
|
T | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0277a0001c0001t0001g0287 | 3 | HG02735.hp1 HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2132-705T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14801512 | ||||||
| chr18:14801543
|
T | C | 19 | a0001c0001t0001g0030a0001c0001t0001g0287a0001c0001t0002g0045others(16): Show | 20 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.2132-674T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14801543 | ||||||
| chr18:14802015
|
GATATA | G | 6 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2132-199_2132-195d others(7): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr18 | 14802015 | |||||
| chr18:14802026
|
A | AATTTTCC others(10874): Show |
1 | a0018c0032t0002g0213 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2193+593_2193+594i others(10883): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | INFO_REALIGN_3_PRIME | chr18 | 14802026 | |||||
| chr18:14802026
|
A | G | 4 | a0001c0001t0002g0081a0001c0001t0003g0087a0001c0003t0002g0123others(1): Show | 4 | HG01175.hp2 NA18906.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.2132-191A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14802026 | ||||||
| chr18:14802112
|
G | T | 1 | a0030c0062t0001g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2132-105G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14802112 | ||||||
| chr18:14802122
|
C | T | 13 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2132-95C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 22/43 | chr18 | 14802122 | ||||||
| chr18:14802654
|
G | C | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2193+376G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14802654 | ||||||
| chr18:14802839
|
A | C | 15 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(12): Show | 15 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2193+561A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14802839 | ||||||
| chr18:14802872
|
A | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(301): Show | 310 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.2193+594A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14802872 | ||||||
| chr18:14802971
|
A | G | 4 | a0001c0001t0002g0045a0001c0001t0002g0046a0018c0032t0002g0213others(1): Show | 4 | HG02040.hp1 NA18986.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.2193+693A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14802971 | ||||||
| chr18:14802995
|
C | T | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2193+717C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14802995 | ||||||
| chr18:14803067
|
G | A | 3 | a0002c0002t0001g0168a0002c0002t0001g0175a0002c0002t0001g0189 | 3 | HG00735.hp2 HG02523.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2194-667G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14803067 | ||||||
| chr18:14803118
|
ATTTCT | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.2194-609_2194-605d others(7): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | INFO_REALIGN_3_PRIME | chr18 | 14803118 | |||||
| chr18:14803123
|
T | TTACTGCA others(10870): Show |
1 | a0004c0007t0001g0309 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2194-610_2194-609i others(10879): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | INFO_REALIGN_3_PRIME | chr18 | 14803123 | |||||
| chr18:14803123
|
T | TTACTGCA others(10871): Show |
1 | a0004c0007t0001g0299 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2194-610_2194-609i others(10880): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | INFO_REALIGN_3_PRIME | chr18 | 14803123 | |||||
| chr18:14803123
|
T | TTACTGCA others(10865): Show |
3 | a0001c0003t0004g0298a0036c0035t0004g0306a0041c0034t0004g0300 | 3 | HG02055.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2194-610_2194-609i others(10874): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | INFO_REALIGN_3_PRIME | chr18 | 14803123 | |||||
| chr18:14803250
|
C | T | 1 | a0035c0054t0001g0258 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2194-484C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14803250 | ||||||
| chr18:14803327
|
T | G | 1 | a0001c0001t0002g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2194-407T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14803327 | ||||||
| chr18:14803348
|
C | T | 79 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.2194-386C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14803348 | ||||||
| chr18:14803376
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(76): Show | 82 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2194-358T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14803376 | ||||||
| chr18:14803625
|
G | A | 118 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(115): Show | 120 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2194-109G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14803625 | ||||||
| chr18:14803681
|
C | T | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(289): Show | 298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.2194-53C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14803681 | ||||||
| chr18:14803691
|
G | A | 1 | a0002c0004t0001g0021 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2194-43G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 23/43 | chr18 | 14803691 | ||||||
| chr18:14803999
|
A | G | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2284+175A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14803999 | ||||||
| chr18:14804016
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2284+192G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804016 | ||||||
| chr18:14804267
|
G | C | 1 | a0004c0022t0001g0301 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2284+443G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804267 | ||||||
| chr18:14804395
|
C | T | 4 | a0002c0004t0001g0037a0011c0014t0001g0086a0011c0014t0001g0264others(1): Show | 4 | HG02145.hp2 NA18972.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.2284+571C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804395 | ||||||
| chr18:14804397
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2284+573G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804397 | ||||||
| chr18:14804546
|
T | C | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2284+722T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804546 | ||||||
| chr18:14804560
|
G | C | 5 | a0005c0005t0001g0302a0005c0005t0006g0232a0005c0005t0006g0233others(2): Show | 5 | HG02723.hp2 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2284+736G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804560 | ||||||
| chr18:14804569
|
T | C | 2 | a0011c0014t0001g0264a0011c0014t0001g0265 | 2 | NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2284+745T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804569 | ||||||
| chr18:14804570
|
G | A | 2 | a0011c0014t0001g0264a0011c0014t0001g0265 | 2 | NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2284+746G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804570 | ||||||
| chr18:14804571
|
C | G | 2 | a0011c0014t0001g0264a0011c0014t0001g0265 | 2 | NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2284+747C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804571 | ||||||
| chr18:14804572
|
T | A | 2 | a0011c0014t0001g0264a0011c0014t0001g0265 | 2 | NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2284+748T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804572 | ||||||
| chr18:14804586
|
T | G | 2 | a0011c0014t0001g0264a0011c0014t0001g0265 | 2 | NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2284+762T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804586 | ||||||
| chr18:14804596
|
T | C | 1 | a0002c0004t0001g0004 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2284+772T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804596 | ||||||
| chr18:14804628
|
G | T | 1 | a0005c0005t0001g0302 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2284+804G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804628 | ||||||
| chr18:14804780
|
T | G | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2284+956T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804780 | ||||||
| chr18:14804843
|
A | T | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2284+1019A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804843 | ||||||
| chr18:14804922
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2284+1098C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804922 | ||||||
| chr18:14804950
|
T | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 162 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2284+1126T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14804950 | ||||||
| chr18:14805023
|
C | T | 1 | a0002c0004t0001g0267 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2284+1199C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805023 | ||||||
| chr18:14805064
|
AAT | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2284+1253_2284+125 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr18 | 14805064 | |||||
| chr18:14805079
|
G | A | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2284+1255G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805079 | ||||||
| chr18:14805084
|
T | A | 1 | a0008c0010t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2284+1260T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805084 | ||||||
| chr18:14805288
|
G | A | 6 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2284+1464G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805288 | ||||||
| chr18:14805289
|
T | C | 2 | a0002c0002t0001g0109a0002c0002t0001g0156 | 2 | NA18994.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2284+1465T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805289 | ||||||
| chr18:14805377
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2284+1553G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805377 | ||||||
| chr18:14805425
|
C | G | 1 | a0002c0002t0001g0098 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2284+1601C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805425 | ||||||
| chr18:14805429
|
G | T | 1 | a0002c0002t0001g0098 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2284+1605G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805429 | ||||||
| chr18:14805481
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2284+1657C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805481 | ||||||
| chr18:14805495
|
G | A | 8 | a0001c0001t0003g0251a0001c0001t0003g0282a0001c0001t0003g0283others(5): Show | 8 | HG00609.hp1 HG02027.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.2284+1671G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805495 | ||||||
| chr18:14805612
|
C | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2284+1788C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805612 | ||||||
| chr18:14805697
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2284+1873T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805697 | ||||||
| chr18:14805727
|
C | T | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2284+1903C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805727 | ||||||
| chr18:14805813
|
A | G | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2284+1989A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805813 | ||||||
| chr18:14805957
|
A | C | 1 | a0002c0004t0001g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2284+2133A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805957 | ||||||
| chr18:14805986
|
C | G | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2284+2162C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805986 | ||||||
| chr18:14805996
|
A | G | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2284+2172A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805996 | ||||||
| chr18:14805996
|
A | T | 1 | a0001c0001t0003g0286 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2284+2172A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14805996 | ||||||
| chr18:14806014
|
A | G | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2284+2190A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806014 | ||||||
| chr18:14806037
|
G | A | 2 | a0001c0003t0004g0303a0040c0033t0004g0304 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2284+2213G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806037 | ||||||
| chr18:14806062
|
T | C | 3 | a0002c0002t0001g0210a0002c0002t0001g0212a0002c0004t0001g0070 | 3 | HG00099.hp1 HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2284+2238T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806062 | ||||||
| chr18:14806145
|
G | A | 5 | a0002c0002t0001g0158a0002c0002t0001g0166a0002c0002t0001g0172others(2): Show | 5 | HG01496.hp1 HG01934.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.2284+2321G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806145 | ||||||
| chr18:14806230
|
G | A | 1 | a0001c0011t0003g0280 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2285-2321G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806230 | ||||||
| chr18:14806230
|
GA | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(157): Show | 163 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2285-2311delA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr18 | 14806230 | |||||
| chr18:14806231
|
A | G | 1 | a0001c0011t0003g0280 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2285-2320A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806231 | ||||||
| chr18:14806237
|
A | G | 2 | a0014c0018t0005g0102a0014c0018t0005g0103 | 2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2285-2314A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806237 | ||||||
| chr18:14806304
|
C | T | 5 | a0008c0010t0001g0262a0008c0010t0008g0006a0011c0014t0001g0086others(2): Show | 5 | HG02145.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2285-2247C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806304 | ||||||
| chr18:14806543
|
G | C | 1 | a0001c0001t0003g0281 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2285-2008G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806543 | ||||||
| chr18:14806628
|
A | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(178): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.2285-1923A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806628 | ||||||
| chr18:14806699
|
C | T | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2285-1852C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806699 | ||||||
| chr18:14806865
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(176): Show | 183 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.2285-1686A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806865 | ||||||
| chr18:14806951
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2285-1600A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806951 | ||||||
| chr18:14806956
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2285-1595C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14806956 | ||||||
| chr18:14807046
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2285-1505G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807046 | ||||||
| chr18:14807069
|
A | T | 2 | a0002c0002t0001g0170a0002c0004t0001g0013 | 2 | HG00621.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2285-1482A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807069 | ||||||
| chr18:14807070
|
T | C | 2 | a0002c0002t0001g0170a0002c0004t0001g0013 | 2 | HG00621.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2285-1481T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807070 | ||||||
| chr18:14807076
|
C | G | 2 | a0002c0002t0001g0170a0002c0004t0001g0013 | 2 | HG00621.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2285-1475C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807076 | ||||||
| chr18:14807170
|
C | T | 3 | a0002c0002t0001g0139a0002c0002t0001g0145a0013c0017t0001g0009 | 3 | HG03453.hp2 NA19077.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2285-1381C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807170 | ||||||
| chr18:14807260
|
G | T | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2285-1291G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807260 | ||||||
| chr18:14807336
|
A | G | 1 | a0002c0002t0001g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2285-1215A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807336 | ||||||
| chr18:14807506
|
A | G | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2285-1045A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807506 | ||||||
| chr18:14807511
|
A | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(288): Show | 296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.2285-1040A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807511 | ||||||
| chr18:14807553
|
A | G | 1 | a0001c0003t0002g0123 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2285-998A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807553 | ||||||
| chr18:14807563
|
G | A | 9 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0169others(6): Show | 9 | HG01123.hp1 HG01255.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2285-988G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807563 | ||||||
| chr18:14807707
|
T | A | 2 | a0014c0018t0005g0102a0014c0018t0005g0103 | 2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2285-844T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807707 | ||||||
| chr18:14807843
|
G | A | 1 | a0002c0002t0001g0164 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2285-708G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807843 | ||||||
| chr18:14807998
|
C | A | 1 | a0002c0002t0001g0167 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2285-553C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14807998 | ||||||
| chr18:14808058
|
G | C | 21 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(18): Show | 21 | HG01167.hp2 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.2285-493G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14808058 | ||||||
| chr18:14808192
|
T | G | 2 | a0003c0006t0008g0236a0024c0038t0008g0238 | 2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2285-359T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14808192 | ||||||
| chr18:14808290
|
A | C | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2285-261A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14808290 | ||||||
| chr18:14808411
|
A | G | 1 | a0010c0027t0001g0135 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2285-140A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14808411 | ||||||
| chr18:14808418
|
A | G | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2285-133A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14808418 | ||||||
| chr18:14808426
|
A | G | 2 | a0002c0002t0001g0167a0002c0004t0001g0267 | 2 | HG01175.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2285-125A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14808426 | ||||||
| chr18:14808532
|
T | C | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2285-19T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14808532 | ||||||
| chr18:14808543
|
T | A | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.2285-8T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 24/43 | chr18 | 14808543 | ||||||
| chr18:14808748
|
A | C | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.2386+4A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14808748 | ||||||
| chr18:14808975
|
G | C | 2 | a0001c0003t0004g0295a0017c0016t0004g0294 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2386+231G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14808975 | ||||||
| chr18:14808994
|
T | A | 1 | a0030c0062t0001g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2386+250T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14808994 | ||||||
| chr18:14809033
|
G | A | 1 | a0001c0003t0004g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2386+289G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809033 | ||||||
| chr18:14809080
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2386+336G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809080 | ||||||
| chr18:14809207
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 162 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2386+463G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809207 | ||||||
| chr18:14809307
|
A | T | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2386+563A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809307 | ||||||
| chr18:14809405
|
C | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 162 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2387-581C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809405 | ||||||
| chr18:14809406
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 162 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2387-580A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809406 | ||||||
| chr18:14809433
|
C | A | 1 | a0021c0042t0005g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2387-553C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809433 | ||||||
| chr18:14809457
|
C | T | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2387-529C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809457 | ||||||
| chr18:14809479
|
A | C | 1 | a0008c0010t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2387-507A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809479 | ||||||
| chr18:14809615
|
T | C | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2387-371T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809615 | ||||||
| chr18:14809689
|
C | T | 5 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2387-297C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809689 | ||||||
| chr18:14809712
|
G | C | 1 | a0001c0003t0004g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2387-274G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809712 | ||||||
| chr18:14809947
|
C | T | 3 | a0001c0001t0003g0087a0001c0001t0003g0241a0001c0001t0003g0243 | 3 | HG02145.hp1 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2387-39C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 26/43 | chr18 | 14809947 | ||||||
| chr18:14810265
|
T | G | 1 | a0027c0028t0001g0165 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2488+85T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810265 | ||||||
| chr18:14810270
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2488+90T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810270 | ||||||
| chr18:14810279
|
T | C | 2 | a0002c0004t0001g0254a0002c0004t0001g0288 | 2 | HG00738.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2488+99T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810279 | ||||||
| chr18:14810418
|
T | C | 1 | a0018c0051t0003g0289 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2488+238T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810418 | ||||||
| chr18:14810430
|
A | G | 2 | a0001c0001t0003g0282a0001c0001t0003g0283 | 2 | HG02083.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2488+250A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810430 | ||||||
| chr18:14810467
|
G | C | 2 | a0001c0001t0003g0282a0001c0001t0003g0283 | 2 | HG02083.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2488+287G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810467 | ||||||
| chr18:14810570
|
T | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2488+390T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810570 | ||||||
| chr18:14810571
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2488+391G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810571 | ||||||
| chr18:14810578
|
T | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2488+398T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810578 | ||||||
| chr18:14810701
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2488+521T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810701 | ||||||
| chr18:14810841
|
T | C | 3 | a0001c0001t0003g0241a0001c0003t0004g0303a0004c0007t0001g0310 | 3 | HG02257.hp2 HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2488+661T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810841 | ||||||
| chr18:14810910
|
C | CGCAGACG others(10871): Show |
1 | a0004c0007t0001g0310 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2488+977_2488+978i others(10880): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | INFO_REALIGN_3_PRIME | chr18 | 14810910 | |||||
| chr18:14810910
|
C | T | 5 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(2): Show | 6 | HG02486.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2488+730C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810910 | ||||||
| chr18:14810969
|
G | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2488+789G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14810969 | ||||||
| chr18:14811180
|
G | C | 29 | a0001c0001t0002g0081a0001c0001t0003g0286a0001c0001t0011g0022others(26): Show | 30 | HG00621.hp1 HG01069.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2488+1000G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811180 | ||||||
| chr18:14811217
|
T | C | 1 | a0030c0062t0001g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2488+1037T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811217 | ||||||
| chr18:14811227
|
C | CTGTCTCG others(10): Show |
1 | a0001c0001t0002g0071 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2488+1059_2488+107 others(21): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | INFO_REALIGN_3_PRIME | chr18 | 14811227 | |||||
| chr18:14811302
|
C | A | 1 | a0001c0003t0002g0151 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2488+1122C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811302 | ||||||
| chr18:14811305
|
G | A | 23 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0084others(20): Show | 23 | HG00099.hp2 HG01167.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2488+1125G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811305 | ||||||
| chr18:14811307
|
C | G | 23 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0084others(20): Show | 23 | HG00099.hp2 HG01167.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2488+1127C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811307 | ||||||
| chr18:14811357
|
G | A | 2 | a0011c0014t0001g0264a0011c0014t0001g0265 | 2 | NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2488+1177G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811357 | ||||||
| chr18:14811360
|
C | T | 13 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(10): Show | 14 | HG01891.hp1 HG02258.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2488+1180C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811360 | ||||||
| chr18:14811368
|
C | T | 5 | a0001c0001t0002g0078a0001c0001t0002g0081a0001c0001t0002g0082others(2): Show | 5 | NA18948.hp1 NA18964.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.2488+1188C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811368 | ||||||
| chr18:14811413
|
A | G | 1 | a0001c0001t0002g0038 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2488+1233A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811413 | ||||||
| chr18:14811428
|
G | A | 3 | a0001c0001t0002g0010a0001c0003t0001g0186a0001c0003t0001g0193 | 3 | HG00642.hp2 HG00738.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2488+1248G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811428 | ||||||
| chr18:14811432
|
T | C | 8 | a0001c0001t0002g0010a0001c0003t0001g0186a0001c0003t0001g0193others(5): Show | 8 | HG00642.hp2 HG00738.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+1252T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811432 | ||||||
| chr18:14811442
|
A | T | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2488+1262A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811442 | ||||||
| chr18:14811503
|
G | A | 1 | a0001c0001t0003g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2488+1323G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811503 | ||||||
| chr18:14811515
|
G | A | 1 | a0002c0002t0001g0182 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2488+1335G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811515 | ||||||
| chr18:14811526
|
C | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2488+1346C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811526 | ||||||
| chr18:14811619
|
G | A | 1 | a0038c0057t0003g0273 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2488+1439G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811619 | ||||||
| chr18:14811749
|
A | G | 1 | a0002c0002t0001g0174 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2489-1355A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811749 | ||||||
| chr18:14811764
|
G | A | 8 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(5): Show | 9 | HG02451.hp2 HG02486.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2489-1340G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811764 | ||||||
| chr18:14811821
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2489-1283T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811821 | ||||||
| chr18:14811976
|
T | C | 1 | a0002c0002t0001g0184 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2489-1128T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14811976 | ||||||
| chr18:14812188
|
C | CAGTCTTT others(33): Show |
1 | a0001c0001t0002g0045 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2489-915_2489-876d others(42): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | INFO_REALIGN_3_PRIME | chr18 | 14812188 | |||||
| chr18:14812293
|
G | T | 5 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2489-811G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14812293 | ||||||
| chr18:14812399
|
T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(73): Show | 79 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.2489-705T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14812399 | ||||||
| chr18:14812410
|
A | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2489-694A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14812410 | ||||||
| chr18:14812430
|
C | T | 12 | a0002c0002t0001g0147a0005c0005t0001g0302a0005c0005t0006g0232others(9): Show | 12 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2489-674C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14812430 | ||||||
| chr18:14812521
|
A | G | 1 | a0002c0002t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2489-583A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14812521 | ||||||
| chr18:14812710
|
G | C | 1 | a0001c0003t0004g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2489-394G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14812710 | ||||||
| chr18:14812713
|
A | G | 1 | a0002c0004t0001g0004 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2489-391A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14812713 | ||||||
| chr18:14812913
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(155): Show | 161 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2489-191A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14812913 | ||||||
| chr18:14812921
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2489-183G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14812921 | ||||||
| chr18:14812999
|
G | T | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2489-105G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14812999 | ||||||
| chr18:14813009
|
C | T | 10 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(7): Show | 11 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2489-95C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 28/43 | chr18 | 14813009 | ||||||
| chr18:14813360
|
C | T | 1 | a0002c0002t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2550+195C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14813360 | ||||||
| chr18:14813541
|
G | C | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2550+376G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14813541 | ||||||
| chr18:14813759
|
A | G | 125 | a0001c0003t0003g0214a0002c0002t0001g0098a0002c0002t0001g0107others(122): Show | 127 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.2550+594A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14813759 | ||||||
| chr18:14813858
|
A | G | 64 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(61): Show | 64 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2550+693A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14813858 | ||||||
| chr18:14813882
|
C | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2550+717C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14813882 | ||||||
| chr18:14814005
|
ATTTCT | A | 114 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(111): Show | 115 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.2551-609_2551-605d others(7): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | INFO_REALIGN_3_PRIME | chr18 | 14814005 | |||||
| chr18:14814006
|
T | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2551-615T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14814006 | ||||||
| chr18:14814101
|
C | T | 1 | a0001c0003t0003g0214 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2551-520C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14814101 | ||||||
| chr18:14814199
|
C | G | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2551-422C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14814199 | ||||||
| chr18:14814235
|
C | T | 3 | a0001c0003t0002g0196a0001c0003t0002g0222a0037c0058t0002g0044 | 3 | NA19079.hp2 NA19081.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2551-386C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14814235 | ||||||
| chr18:14814263
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(76): Show | 82 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2551-358T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14814263 | ||||||
| chr18:14814276
|
A | G | 1 | a0001c0003t0004g0307 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2551-345A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14814276 | ||||||
| chr18:14814341
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2551-280G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14814341 | ||||||
| chr18:14814512
|
A | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(289): Show | 298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.2551-109A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14814512 | ||||||
| chr18:14814568
|
T | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.2551-53T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 29/43 | chr18 | 14814568 | ||||||
| chr18:14814652
|
G | GGTGTTTA others(10875): Show |
2 | a0010c0026t0001g0121a0010c0049t0001g0053 | 2 | HG02738.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.2641+735_2641+736i others(10884): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr18 | 14814652 | |||||
| chr18:14814652
|
G | GGTGTTTA others(10875): Show |
1 | a0010c0027t0001g0135 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2641+735_2641+736i others(10884): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr18 | 14814652 | |||||
| chr18:14815346
|
A | G | 1 | a0002c0002t0001g0166 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2641+635A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815346 | ||||||
| chr18:14815377
|
C | T | 3 | a0001c0003t0004g0298a0036c0035t0004g0306a0041c0034t0004g0300 | 3 | HG02055.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2641+666C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815377 | ||||||
| chr18:14815412
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2641+701T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815412 | ||||||
| chr18:14815471
|
GAGGAGAG others(50): Show |
G | 1 | a0001c0001t0002g0041 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2641+781_2641+837d others(59): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr18 | 14815471 | |||||
| chr18:14815492
|
A | G | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2641+781A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815492 | ||||||
| chr18:14815549
|
G | C | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2641+838G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815549 | ||||||
| chr18:14815578
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(77): Show | 80 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2641+867G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815578 | ||||||
| chr18:14815684
|
C | A | 2 | a0001c0001t0004g0290a0001c0001t0004g0291 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2641+973C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815684 | ||||||
| chr18:14815714
|
G | C | 26 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(23): Show | 27 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.2641+1003G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815714 | ||||||
| chr18:14815734
|
G | A | 1 | a0038c0057t0003g0273 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2641+1023G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815734 | ||||||
| chr18:14815820
|
G | C | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2641+1109G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815820 | ||||||
| chr18:14815839
|
C | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2641+1128C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815839 | ||||||
| chr18:14815965
|
A | G | 1 | a0001c0001t0003g0281 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2641+1254A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14815965 | ||||||
| chr18:14816037
|
A | T | 1 | a0001c0001t0002g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2641+1326A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816037 | ||||||
| chr18:14816135
|
A | C | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2641+1424A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816135 | ||||||
| chr18:14816151
|
C | T | 2 | a0001c0003t0002g0216a0001c0003t0002g0217 | 2 | HG01257.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2641+1440C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816151 | ||||||
| chr18:14816210
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 162 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2641+1499C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816210 | ||||||
| chr18:14816331
|
A | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2641+1620A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816331 | ||||||
| chr18:14816367
|
C | T | 1 | a0030c0062t0001g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2641+1656C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816367 | ||||||
| chr18:14816473
|
G | A | 1 | a0005c0005t0006g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2641+1762G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816473 | ||||||
| chr18:14816512
|
G | T | 5 | a0001c0001t0002g0110a0001c0003t0002g0106a0001c0003t0002g0111others(2): Show | 5 | HG01074.hp2 HG01109.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2641+1801G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816512 | ||||||
| chr18:14816514
|
T | G | 5 | a0001c0001t0002g0110a0001c0003t0002g0106a0001c0003t0002g0111others(2): Show | 5 | HG01074.hp2 HG01109.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2641+1803T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816514 | ||||||
| chr18:14816642
|
G | GA | 11 | a0001c0001t0004g0290a0001c0001t0004g0291a0002c0002t0001g0167others(8): Show | 11 | HG01175.hp1 HG02135.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2641+1949dupA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr18 | 14816642 | |||||
| chr18:14816642
|
GA | G | 17 | a0001c0001t0002g0019a0001c0003t0001g0193a0004c0007t0001g0005others(14): Show | 18 | HG00738.hp1 HG01243.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.2641+1949delA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr18 | 14816642 | |||||
| chr18:14816651
|
A | G | 1 | a0001c0001t0002g0073 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2641+1940A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816651 | ||||||
| chr18:14816775
|
C | T | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2641+2064C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816775 | ||||||
| chr18:14816856
|
G | T | 1 | a0028c0025t0001g0202 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2641+2145G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816856 | ||||||
| chr18:14816929
|
A | C | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2641+2218A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816929 | ||||||
| chr18:14816975
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2641+2264G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14816975 | ||||||
| chr18:14817012
|
G | A | 1 | a0001c0001t0003g0286 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2641+2301G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817012 | ||||||
| chr18:14817136
|
C | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2641+2425C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817136 | ||||||
| chr18:14817357
|
C | T | 1 | a0042c0052t0001g0079 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2641+2646C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817357 | ||||||
| chr18:14817392
|
A | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2641+2681A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817392 | ||||||
| chr18:14817396
|
G | A | 1 | a0002c0002t0001g0117 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2641+2685G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817396 | ||||||
| chr18:14817455
|
A | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2641+2744A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817455 | ||||||
| chr18:14817458
|
A | T | 2 | a0001c0001t0003g0251a0001c0001t0003g0285 | 2 | NA18990.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2641+2747A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817458 | ||||||
| chr18:14817541
|
A | G | 1 | a0036c0035t0004g0306 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2641+2830A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817541 | ||||||
| chr18:14817542
|
T | C | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2641+2831T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817542 | ||||||
| chr18:14817635
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2641+2924T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817635 | ||||||
| chr18:14817720
|
G | A | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2641+3009G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817720 | ||||||
| chr18:14817926
|
G | C | 2 | a0008c0010t0001g0262a0008c0010t0008g0006 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2641+3215G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817926 | ||||||
| chr18:14817995
|
G | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(182): Show | 189 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.2641+3284G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14817995 | ||||||
| chr18:14818053
|
G | A | 23 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(20): Show | 24 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.2641+3342G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818053 | ||||||
| chr18:14818087
|
A | G | 3 | a0002c0002t0001g0199a0002c0002t0001g0200a0028c0025t0001g0202 | 3 | NA18981.hp2 NA19002.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2641+3376A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818087 | ||||||
| chr18:14818133
|
A | G | 3 | a0001c0003t0001g0125a0001c0003t0001g0126a0001c0003t0001g0127 | 3 | HG01069.hp2 HG01192.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2641+3422A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818133 | ||||||
| chr18:14818292
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 162 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2641+3581A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818292 | ||||||
| chr18:14818531
|
TC | T | 27 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0119others(24): Show | 28 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.2641+3824delC | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr18 | 14818531 | |||||
| chr18:14818557
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0277 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2641+3846T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818557 | ||||||
| chr18:14818574
|
A | G | 1 | a0014c0018t0005g0103 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2641+3863A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818574 | ||||||
| chr18:14818582
|
T | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(304): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.2641+3871T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818582 | ||||||
| chr18:14818589
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(76): Show | 82 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2641+3878C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818589 | ||||||
| chr18:14818608
|
G | A | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2642-3875G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818608 | ||||||
| chr18:14818673
|
C | A | 1 | a0002c0002t0001g0141 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2642-3810C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818673 | ||||||
| chr18:14818757
|
A | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2642-3726A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818757 | ||||||
| chr18:14818765
|
T | G | 1 | a0001c0011t0003g0280 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2642-3718T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818765 | ||||||
| chr18:14818781
|
T | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2642-3702T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818781 | ||||||
| chr18:14818827
|
T | A | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2642-3656T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818827 | ||||||
| chr18:14818837
|
G | A | 12 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(9): Show | 13 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2642-3646G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818837 | ||||||
| chr18:14818837
|
G | T | 4 | a0001c0001t0001g0256a0001c0001t0003g0087a0001c0001t0003g0241others(1): Show | 4 | HG01106.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2642-3646G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818837 | ||||||
| chr18:14818896
|
C | A | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2642-3587C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818896 | ||||||
| chr18:14818966
|
A | G | 2 | a0004c0022t0001g0301a0004c0045t0010g0089 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2642-3517A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818966 | ||||||
| chr18:14818985
|
C | A | 1 | a0002c0002t0001g0178 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2642-3498C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14818985 | ||||||
| chr18:14819008
|
T | A | 1 | a0004c0007t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2642-3475T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819008 | ||||||
| chr18:14819188
|
C | T | 1 | a0001c0011t0003g0280 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2642-3295C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819188 | ||||||
| chr18:14819217
|
T | A | 15 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(12): Show | 15 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2642-3266T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819217 | ||||||
| chr18:14819390
|
T | G | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2642-3093T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819390 | ||||||
| chr18:14819441
|
C | T | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2642-3042C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819441 | ||||||
| chr18:14819464
|
TAG | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2642-3018_2642-301 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819464 | ||||||
| chr18:14819466
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(178): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.2642-3017G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819466 | ||||||
| chr18:14819485
|
T | C | 2 | a0002c0002t0001g0116a0002c0002t0001g0208 | 2 | HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.2642-2998T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819485 | ||||||
| chr18:14819495
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0025others(6): Show | 10 | HG00738.hp1 HG01074.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2642-2988G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819495 | ||||||
| chr18:14819509
|
G | A | 7 | a0003c0006t0001g0003a0003c0006t0001g0237a0003c0006t0001g0240others(4): Show | 8 | HG02055.hp1 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2642-2974G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819509 | ||||||
| chr18:14819599
|
G | A | 1 | a0019c0020t0001g0234 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2642-2884G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819599 | ||||||
| chr18:14819660
|
A | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2642-2823A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819660 | ||||||
| chr18:14819671
|
G | C | 1 | a0001c0001t0001g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2642-2812G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819671 | ||||||
| chr18:14819700
|
C | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(182): Show | 189 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.2642-2783C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819700 | ||||||
| chr18:14819837
|
G | A | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2642-2646G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819837 | ||||||
| chr18:14819839
|
G | C | 4 | a0001c0001t0001g0256a0001c0003t0001g0186a0001c0041t0001g0249others(1): Show | 4 | HG00642.hp2 HG01106.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2642-2644G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819839 | ||||||
| chr18:14819938
|
G | C | 2 | a0009c0013t0005g0104a0009c0013t0005g0105 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2642-2545G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819938 | ||||||
| chr18:14819944
|
A | T | 2 | a0009c0013t0005g0104a0009c0013t0005g0105 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2642-2539A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819944 | ||||||
| chr18:14819946
|
C | G | 2 | a0009c0013t0005g0104a0009c0013t0005g0105 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2642-2537C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819946 | ||||||
| chr18:14819953
|
C | T | 2 | a0009c0013t0005g0104a0009c0013t0005g0105 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2642-2530C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14819953 | ||||||
| chr18:14820036
|
A | C | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2642-2447A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14820036 | ||||||
| chr18:14820116
|
T | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2642-2367T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14820116 | ||||||
| chr18:14820158
|
CTGTT | C | 7 | a0001c0003t0002g0157a0008c0010t0001g0261a0008c0010t0001g0262others(4): Show | 7 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2642-2321_2642-231 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr18 | 14820158 | |||||
| chr18:14820273
|
G | A | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2642-2210G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14820273 | ||||||
| chr18:14820299
|
C | T | 65 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2642-2184C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14820299 | ||||||
| chr18:14820433
|
A | C | 2 | a0002c0002t0001g0209a0002c0004t0001g0284 | 2 | HG02165.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2642-2050A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14820433 | ||||||
| chr18:14820473
|
C | A | 1 | a0001c0001t0002g0038 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2642-2010C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14820473 | ||||||
| chr18:14820572
|
AG | A | 6 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2642-1908delG | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr18 | 14820572 | |||||
| chr18:14820627
|
T | G | 1 | a0001c0001t0002g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2642-1856T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14820627 | ||||||
| chr18:14821104
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(296): Show | 304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.2642-1379A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821104 | ||||||
| chr18:14821199
|
C | T | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2642-1284C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821199 | ||||||
| chr18:14821278
|
C | T | 4 | a0001c0001t0001g0256a0001c0003t0001g0186a0001c0041t0001g0249others(1): Show | 4 | HG00642.hp2 HG01106.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2642-1205C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821278 | ||||||
| chr18:14821341
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(157): Show | 163 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2642-1142G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821341 | ||||||
| chr18:14821419
|
T | A | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2642-1064T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821419 | ||||||
| chr18:14821669
|
G | C | 1 | a0001c0001t0002g0043 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2642-814G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821669 | ||||||
| chr18:14821779
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0039 | 3 | NA19007.hp1 NA19010.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2642-704A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821779 | ||||||
| chr18:14821791
|
T | G | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2642-692T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821791 | ||||||
| chr18:14821923
|
T | C | 1 | a0002c0002t0001g0176 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2642-560T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821923 | ||||||
| chr18:14821963
|
T | G | 26 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0119others(23): Show | 27 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.2642-520T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821963 | ||||||
| chr18:14821983
|
C | T | 12 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(9): Show | 13 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2642-500C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14821983 | ||||||
| chr18:14822037
|
TGTA | T | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2642-442_2642-440d others(5): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr18 | 14822037 | |||||
| chr18:14822102
|
T | C | 1 | a0001c0003t0002g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2642-381T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14822102 | ||||||
| chr18:14822319
|
T | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(182): Show | 189 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.2642-164T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14822319 | ||||||
| chr18:14822391
|
G | T | 1 | a0002c0002t0001g0248 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2642-92G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14822391 | ||||||
| chr18:14822446
|
T | G | 2 | a0001c0003t0004g0295a0017c0016t0004g0294 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2642-37T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 30/43 | chr18 | 14822446 | ||||||
| chr18:14822754
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2743+77C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14822754 | ||||||
| chr18:14822759
|
G | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2743+82G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14822759 | ||||||
| chr18:14822779
|
G | T | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2743+102G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14822779 | ||||||
| chr18:14822942
|
TACGTGCT others(356): Show |
T | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(306): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.2743+280_2743+642d others(2): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14822942 | |||||
| chr18:14823579
|
G | A | 65 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2743+902G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14823579 | ||||||
| chr18:14823664
|
C | T | 65 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2743+987C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14823664 | ||||||
| chr18:14823896
|
A | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2743+1219A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14823896 | ||||||
| chr18:14823914
|
G | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2743+1237G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14823914 | ||||||
| chr18:14823962
|
TC | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2743+1288delC | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14823962 | |||||
| chr18:14824110
|
C | CT | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(151): Show | 157 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.2743+1442dupT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14824110 | |||||
| chr18:14824110
|
CT | C | 114 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(111): Show | 115 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.2743+1442delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14824110 | |||||
| chr18:14824120
|
A | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 162 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.2743+1443A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14824120 | ||||||
| chr18:14824150
|
C | T | 1 | a0001c0001t0004g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2743+1473C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14824150 | ||||||
| chr18:14824160
|
C | T | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2743+1483C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14824160 | ||||||
| chr18:14824192
|
TTAACTC | T | 114 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0109others(111): Show | 115 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.2743+1519_2743+152 others(10): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14824192 | |||||
| chr18:14824272
|
C | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2743+1595C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14824272 | ||||||
| chr18:14824317
|
A | C | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2743+1640A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14824317 | ||||||
| chr18:14824436
|
CT | C | 64 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(61): Show | 64 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2743+1760delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14824436 | ||||||
| chr18:14824437
|
T | C | 1 | a0037c0058t0002g0044 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2743+1760T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14824437 | ||||||
| chr18:14824619
|
T | C | 1 | a0004c0022t0001g0301 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2743+1942T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14824619 | ||||||
| chr18:14824756
|
C | A | 13 | a0002c0002t0001g0109a0002c0002t0001g0141a0002c0002t0001g0146others(10): Show | 13 | NA18944.hp2 NA18948.hp2 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.2743+2079C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14824756 | ||||||
| chr18:14824995
|
G | A | 1 | a0002c0004t0001g0267 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2743+2318G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14824995 | ||||||
| chr18:14825213
|
A | C | 1 | a0023c0043t0001g0095 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2743+2536A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14825213 | ||||||
| chr18:14825266
|
G | A | 1 | a0002c0002t0001g0137 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2743+2589G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14825266 | ||||||
| chr18:14825553
|
A | G | 2 | a0001c0001t0004g0290a0001c0001t0004g0291 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2744-2725A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14825553 | ||||||
| chr18:14825615
|
A | G | 2 | a0006c0008t0001g0163a0006c0008t0001g0171 | 2 | HG01952.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2744-2663A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14825615 | ||||||
| chr18:14825731
|
G | A | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2744-2547G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14825731 | ||||||
| chr18:14825849
|
T | C | 1 | a0040c0033t0004g0304 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2744-2429T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14825849 | ||||||
| chr18:14825962
|
G | T | 1 | a0002c0002t0001g0115 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2744-2316G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14825962 | ||||||
| chr18:14825969
|
GCAAA | G | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2744-2306_2744-230 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14825969 | |||||
| chr18:14825995
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2744-2283G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14825995 | ||||||
| chr18:14826245
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2744-2033G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826245 | ||||||
| chr18:14826383
|
A | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2744-1895A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826383 | ||||||
| chr18:14826477
|
G | A | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2744-1801G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826477 | ||||||
| chr18:14826532
|
T | G | 1 | a0001c0003t0001g0127 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2744-1746T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826532 | ||||||
| chr18:14826544
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2744-1734G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826544 | ||||||
| chr18:14826661
|
TCTCTCTC others(9): Show |
T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2744-1603_2744-158 others(20): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826661 | |||||
| chr18:14826677
|
C | CCT | 4 | a0007c0009t0007g0129a0007c0009t0007g0226a0030c0062t0001g0094others(1): Show | 4 | HG01891.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2744-1585_2744-158 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826677 | |||||
| chr18:14826678
|
CTCT | C | 4 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0084others(1): Show | 4 | HG02683.hp1 HG03491.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2744-1599_2744-159 others(7): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826678 | ||||||
| chr18:14826679
|
T | C | 2 | a0002c0002t0001g0181a0002c0002t0001g0182 | 2 | HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2744-1599T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826679 | ||||||
| chr18:14826689
|
T | TCACACAC others(5): Show |
1 | a0001c0001t0001g0260 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2744-1588_2744-158 others(16): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826689 | |||||
| chr18:14826691
|
T | A | 1 | a0001c0001t0001g0260 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2744-1587T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826691 | ||||||
| chr18:14826691
|
T | TCACA | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0034others(7): Show | 11 | HG02735.hp1 HG02886.hp1 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.2744-1586_2744-158 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826691 | |||||
| chr18:14826691
|
T | TCACACA | 6 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG01106.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2744-1586_2744-158 others(10): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826691 | |||||
| chr18:14826691
|
T | TCACACAC others(1): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0025others(10): Show | 15 | HG00544.hp2 HG00642.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.2744-1586_2744-158 others(12): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826691 | |||||
| chr18:14826691
|
T | TCACACAC others(3): Show |
22 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0024others(19): Show | 23 | HG00621.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2744-1586_2744-158 others(14): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826691 | |||||
| chr18:14826691
|
T | TCACACAC others(5): Show |
6 | a0001c0001t0001g0253a0001c0001t0001g0263a0001c0003t0001g0125others(3): Show | 6 | HG00735.hp1 HG01069.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2744-1586_2744-158 others(16): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826691 | |||||
| chr18:14826691
|
T | TCACACAC others(7): Show |
6 | a0001c0001t0001g0252a0001c0001t0001g0259a0001c0001t0003g0085others(3): Show | 6 | HG02965.hp1 HG03942.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.2744-1586_2744-158 others(18): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826691 | |||||
| chr18:14826691
|
T | TCACACAC others(9): Show |
6 | a0001c0001t0003g0250a0001c0001t0003g0286a0001c0001t0013g0242others(3): Show | 6 | HG00609.hp1 HG02027.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.2744-1586_2744-158 others(20): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826691 | |||||
| chr18:14826691
|
T | TCACACAC others(11): Show |
1 | a0001c0001t0003g0283 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2744-1586_2744-158 others(22): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826691 | |||||
| chr18:14826691
|
T | TCACACAC others(13): Show |
1 | a0001c0001t0003g0282 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2744-1586_2744-158 others(24): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826691 | |||||
| chr18:14826693
|
T | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(71): Show | 78 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.2744-1585T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826693 | ||||||
| chr18:14826693
|
T | TCACACAC others(3): Show |
4 | a0001c0011t0003g0223a0001c0011t0003g0270a0001c0011t0003g0274others(1): Show | 4 | HG01123.hp2 HG01978.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.2744-1560_2744-155 others(14): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCACACAC others(5): Show |
8 | a0001c0001t0003g0087a0001c0001t0003g0241a0001c0001t0003g0243others(5): Show | 9 | HG01952.hp1 HG02074.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2744-1562_2744-155 others(16): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCACACAC others(9): Show |
1 | a0010c0026t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2744-1566_2744-155 others(20): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCA | 3 | a0007c0009t0007g0227a0014c0018t0005g0102a0014c0018t0005g0103 | 3 | HG02258.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2744-1584_2744-158 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCACAC others(3): Show |
9 | a0002c0002t0001g0107a0002c0002t0001g0174a0002c0002t0001g0184others(6): Show | 9 | HG00323.hp1 HG00673.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.2744-1584_2744-158 others(14): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCACAC others(5): Show |
28 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0119others(25): Show | 28 | HG00099.hp1 HG00544.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.2744-1584_2744-158 others(16): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCACAC others(7): Show |
50 | a0002c0002t0001g0098a0002c0002t0001g0109a0002c0002t0001g0115others(47): Show | 50 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2744-1584_2744-158 others(18): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCACAC others(9): Show |
8 | a0002c0002t0001g0130a0002c0002t0001g0132a0002c0002t0001g0166others(5): Show | 8 | HG01517.hp1 HG01934.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2744-1584_2744-158 others(20): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCACAC others(11): Show |
2 | a0002c0002t0001g0156a0020c0040t0001g0206 | 2 | HG03688.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2744-1584_2744-158 others(22): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCACAC others(13): Show |
2 | a0006c0008t0001g0190a0006c0008t0001g0219 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2744-1584_2744-158 others(24): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCTCAC others(1): Show |
5 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0310others(2): Show | 6 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2744-1584_2744-158 others(12): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCTCAC others(3): Show |
1 | a0004c0007t0001g0309 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2744-1584_2744-158 others(14): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCTCAC others(5): Show |
1 | a0011c0014t0001g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2744-1584_2744-158 others(16): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCTCAC others(7): Show |
8 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0150others(5): Show | 8 | HG00738.hp2 HG02698.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.2744-1584_2744-158 others(18): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
T | TCTCTCTC others(11): Show |
2 | a0011c0014t0001g0264a0011c0014t0001g0265 | 2 | NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2744-1584_2744-158 others(22): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
TCA | T | 59 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0017others(56): Show | 59 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.2744-1552_2744-155 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
TCACA | T | 9 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(6): Show | 9 | HG02055.hp2 HG02647.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2744-1554_2744-155 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826693
|
TCACACA | T | 6 | a0001c0003t0004g0295a0001c0003t0004g0296a0001c0003t0004g0305others(3): Show | 6 | HG01167.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2744-1556_2744-155 others(10): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826693 | |||||
| chr18:14826695
|
A | T | 11 | a0001c0001t0002g0015a0001c0001t0002g0066a0001c0001t0002g0067others(8): Show | 11 | HG01175.hp2 HG01243.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2744-1583A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826695 | ||||||
| chr18:14826697
|
A | T | 65 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0016others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2744-1581A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826697 | ||||||
| chr18:14826699
|
A | T | 63 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0017others(60): Show | 63 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.2744-1579A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826699 | ||||||
| chr18:14826701
|
A | T | 6 | a0001c0001t0002g0048a0001c0001t0002g0078a0001c0001t0002g0081others(3): Show | 6 | NA18942.hp1 NA18948.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.2744-1577A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826701 | ||||||
| chr18:14826728
|
A | C | 5 | a0001c0001t0001g0030a0001c0001t0003g0251a0001c0001t0003g0285others(2): Show | 5 | HG02735.hp1 NA18939.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.2744-1550A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14826728 | ||||||
| chr18:14826823
|
CT | C | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2744-1448delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr18 | 14826823 | |||||
| chr18:14827016
|
A | T | 1 | a0017c0016t0003g0148 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2744-1262A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14827016 | ||||||
| chr18:14827579
|
G | A | 1 | a0008c0010t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2744-699G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14827579 | ||||||
| chr18:14827721
|
A | G | 1 | a0031c0047t0001g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2744-557A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14827721 | ||||||
| chr18:14827751
|
C | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2744-527C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14827751 | ||||||
| chr18:14827955
|
T | C | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2744-323T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14827955 | ||||||
| chr18:14828017
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2744-261A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14828017 | ||||||
| chr18:14828073
|
G | A | 1 | a0002c0004t0001g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2744-205G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14828073 | ||||||
| chr18:14828135
|
A | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2744-143A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14828135 | ||||||
| chr18:14828159
|
C | T | 1 | a0001c0003t0002g0097 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2744-119C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14828159 | ||||||
| chr18:14828275
|
T | C | 2 | a0001c0001t0003g0282a0001c0001t0003g0283 | 2 | HG02083.hp1 HG02129.hp1 |
splice_region_variant&intron_variant | LOW | c.2744-3T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 32/43 | chr18 | 14828275 | ||||||
| chr18:14828406
|
C | T | 2 | a0002c0004t0001g0288a0013c0017t0001g0009 | 2 | HG02698.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2774+98C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14828406 | ||||||
| chr18:14828447
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(76): Show | 82 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2774+139C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14828447 | ||||||
| chr18:14828545
|
C | T | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2774+237C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14828545 | ||||||
| chr18:14828635
|
G | A | 3 | a0001c0003t0004g0298a0036c0035t0004g0306a0041c0034t0004g0300 | 3 | HG02055.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2774+327G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14828635 | ||||||
| chr18:14828679
|
A | G | 2 | a0001c0001t0003g0251a0001c0001t0003g0285 | 2 | NA18990.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2774+371A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14828679 | ||||||
| chr18:14828872
|
C | T | 3 | a0001c0001t0002g0045a0001c0001t0002g0046a0037c0058t0002g0044 | 3 | HG02040.hp1 NA19082.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2774+564C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14828872 | ||||||
| chr18:14828943
|
T | C | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2774+635T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14828943 | ||||||
| chr18:14828944
|
T | A | 1 | a0035c0054t0001g0258 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2774+636T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14828944 | ||||||
| chr18:14829172
|
C | T | 1 | a0005c0005t0006g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2774+864C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14829172 | ||||||
| chr18:14829258
|
A | G | 3 | a0011c0014t0001g0086a0011c0014t0001g0264a0011c0014t0001g0265 | 3 | HG02145.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2774+950A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14829258 | ||||||
| chr18:14829384
|
T | C | 1 | a0018c0032t0002g0213 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2774+1076T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14829384 | ||||||
| chr18:14830198
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2775-1185T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14830198 | ||||||
| chr18:14830275
|
A | T | 1 | a0001c0001t0013g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2775-1108A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14830275 | ||||||
| chr18:14830320
|
G | A | 2 | a0002c0002t0001g0209a0002c0004t0001g0284 | 2 | HG02165.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2775-1063G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14830320 | ||||||
| chr18:14830587
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2775-796A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14830587 | ||||||
| chr18:14830677
|
A | G | 1 | a0008c0010t0008g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2775-706A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14830677 | ||||||
| chr18:14831051
|
G | A | 1 | a0002c0002t0001g0225 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2775-332G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14831051 | ||||||
| chr18:14831096
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(182): Show | 189 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.2775-287A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14831096 | ||||||
| chr18:14831141
|
T | C | 6 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(3): Show | 6 | HG02258.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2775-242T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14831141 | ||||||
| chr18:14831167
|
G | C | 1 | a0001c0011t0003g0223 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2775-216G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14831167 | ||||||
| chr18:14831181
|
G | GA | 36 | a0002c0002t0001g0118a0002c0002t0001g0136a0002c0002t0001g0142others(33): Show | 37 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2775-183dupA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | INFO_REALIGN_3_PRIME | chr18 | 14831181 | |||||
| chr18:14831181
|
G | GAA | 7 | a0003c0006t0001g0237a0003c0021t0001g0239a0004c0007t0001g0005others(4): Show | 8 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2775-184_2775-183d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | INFO_REALIGN_3_PRIME | chr18 | 14831181 | |||||
| chr18:14831181
|
G | GAAAA | 8 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(5): Show | 8 | HG01243.hp1 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2775-186_2775-183d others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | INFO_REALIGN_3_PRIME | chr18 | 14831181 | |||||
| chr18:14831181
|
G | GAAAAAAA others(3): Show |
52 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0027others(49): Show | 53 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.2775-192_2775-183d others(12): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | INFO_REALIGN_3_PRIME | chr18 | 14831181 | |||||
| chr18:14831181
|
G | GAAAAAAA others(4): Show |
78 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(75): Show | 78 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.2775-193_2775-183d others(13): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | INFO_REALIGN_3_PRIME | chr18 | 14831181 | |||||
| chr18:14831181
|
G | GAAAAAAA others(5): Show |
24 | a0001c0001t0002g0051a0001c0001t0002g0276a0001c0001t0003g0055others(21): Show | 24 | HG00423.hp1 HG00735.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2775-194_2775-183d others(14): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | INFO_REALIGN_3_PRIME | chr18 | 14831181 | |||||
| chr18:14831181
|
G | GAAAAAAA others(6): Show |
2 | a0001c0001t0003g0250a0038c0057t0003g0273 | 2 | HG02572.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2775-195_2775-183d others(15): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | INFO_REALIGN_3_PRIME | chr18 | 14831181 | |||||
| chr18:14831181
|
G | GAAAAAAA others(26): Show |
2 | a0011c0014t0001g0086a0011c0014t0001g0264 | 2 | HG02145.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.2775-183_2775-182i others(35): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | INFO_REALIGN_3_PRIME | chr18 | 14831181 | |||||
| chr18:14831181
|
G | GAAAAAAA others(28): Show |
1 | a0011c0014t0001g0265 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2775-183_2775-182i others(37): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | INFO_REALIGN_3_PRIME | chr18 | 14831181 | |||||
| chr18:14831181
|
G | GGAAAAAA others(3): Show |
3 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0292 | 5 | HG01167.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2775-202_2775-201i others(12): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14831181 | ||||||
| chr18:14831181
|
G | GGAAAAAA others(4): Show |
1 | a0035c0054t0001g0258 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2775-202_2775-201i others(13): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14831181 | ||||||
| chr18:14831234
|
G | T | 1 | a0008c0010t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2775-149G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 33/43 | chr18 | 14831234 | ||||||
| chr18:14831464
|
G | T | 5 | a0008c0010t0001g0262a0008c0010t0008g0006a0008c0010t0008g0007others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2847+9G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14831464 | ||||||
| chr18:14831647
|
T | C | 1 | a0043c0039t0009g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2847+192T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14831647 | ||||||
| chr18:14831770
|
A | G | 4 | a0008c0010t0001g0262a0008c0010t0008g0006a0008c0010t0008g0007others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2847+315A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14831770 | ||||||
| chr18:14831952
|
C | T | 1 | a0002c0002t0001g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2847+497C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14831952 | ||||||
| chr18:14831961
|
T | C | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2847+506T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14831961 | ||||||
| chr18:14832040
|
TTTAA | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2847+590_2847+593d others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr18 | 14832040 | |||||
| chr18:14832095
|
G | T | 1 | a0002c0004t0001g0029 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2847+640G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832095 | ||||||
| chr18:14832212
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(160): Show | 166 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.2847+757T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832212 | ||||||
| chr18:14832238
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(76): Show | 82 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.2847+783C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832238 | ||||||
| chr18:14832477
|
T | C | 1 | a0002c0002t0001g0116 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2847+1022T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832477 | ||||||
| chr18:14832618
|
C | T | 1 | a0011c0014t0001g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2847+1163C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832618 | ||||||
| chr18:14832775
|
A | G | 1 | a0043c0039t0009g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2847+1320A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832775 | ||||||
| chr18:14832781
|
G | A | 1 | a0004c0045t0010g0089 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2847+1326G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832781 | ||||||
| chr18:14832831
|
T | C | 1 | a0001c0001t0004g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2847+1376T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832831 | ||||||
| chr18:14832859
|
A | G | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2847+1404A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832859 | ||||||
| chr18:14832911
|
T | G | 1 | a0001c0001t0003g0269 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2847+1456T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832911 | ||||||
| chr18:14832999
|
T | C | 1 | a0001c0003t0002g0188 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2847+1544T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14832999 | ||||||
| chr18:14833158
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0025others(6): Show | 10 | HG00738.hp1 HG01074.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2847+1703A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14833158 | ||||||
| chr18:14833171
|
G | A | 3 | a0001c0001t0002g0045a0001c0001t0002g0046a0037c0058t0002g0044 | 3 | HG02040.hp1 NA19082.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2847+1716G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14833171 | ||||||
| chr18:14833389
|
C | T | 1 | a0036c0035t0004g0306 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2847+1934C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14833389 | ||||||
| chr18:14833398
|
G | A | 1 | a0013c0017t0005g0101 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2847+1943G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14833398 | ||||||
| chr18:14833441
|
G | A | 1 | a0013c0017t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2847+1986G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14833441 | ||||||
| chr18:14833822
|
C | G | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(304): Show | 313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.2847+2367C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14833822 | ||||||
| chr18:14833832
|
C | G | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2847+2377C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14833832 | ||||||
| chr18:14833871
|
G | T | 1 | a0001c0001t0001g0293 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2847+2416G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14833871 | ||||||
| chr18:14833890
|
T | A | 1 | a0030c0062t0001g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2847+2435T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14833890 | ||||||
| chr18:14834083
|
C | G | 1 | a0001c0003t0004g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2847+2628C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14834083 | ||||||
| chr18:14834102
|
G | A | 6 | a0002c0002t0001g0119a0002c0002t0001g0174a0002c0002t0001g0184others(3): Show | 7 | HG00642.hp1 HG01069.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.2847+2647G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14834102 | ||||||
| chr18:14834600
|
A | G | 1 | a0001c0001t0003g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2848-2611A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14834600 | ||||||
| chr18:14834611
|
G | A | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2848-2600G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14834611 | ||||||
| chr18:14834911
|
A | C | 2 | a0001c0003t0002g0196a0001c0003t0002g0222 | 2 | NA19079.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2848-2300A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14834911 | ||||||
| chr18:14835296
|
G | A | 4 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2848-1915G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14835296 | ||||||
| chr18:14835307
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(175): Show | 182 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.2848-1904G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14835307 | ||||||
| chr18:14835342
|
A | G | 1 | a0001c0063t0004g0297 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2848-1869A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14835342 | ||||||
| chr18:14835668
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(296): Show | 304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.2848-1543A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14835668 | ||||||
| chr18:14835706
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2848-1505G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14835706 | ||||||
| chr18:14835945
|
A | C | 1 | a0002c0004t0001g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2848-1266A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14835945 | ||||||
| chr18:14836385
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(75): Show | 81 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.2848-826A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14836385 | ||||||
| chr18:14836391
|
C | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(75): Show | 81 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.2848-820C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14836391 | ||||||
| chr18:14836840
|
G | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(173): Show | 179 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.2848-371G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14836840 | ||||||
| chr18:14837169
|
GT | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(155): Show | 161 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2848-32delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr18 | 14837169 | |||||
| chr18:14837185
|
T | A | 4 | a0001c0003t0004g0296a0001c0003t0004g0305a0001c0003t0004g0307others(1): Show | 4 | HG01167.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2848-26T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 34/43 | chr18 | 14837185 | ||||||
| chr18:14837362
|
T | C | 2 | a0001c0001t0001g0031a0001c0003t0001g0195 | 2 | NA18964.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2926+73T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 35/43 | chr18 | 14837362 | ||||||
| chr18:14837472
|
G | T | 1 | a0001c0003t0001g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2927-143G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 35/43 | chr18 | 14837472 | ||||||
| chr18:14837686
|
A | ATTG | 23 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(20): Show | 24 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.2988+22_2988+24dup others(3): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | INFO_REALIGN_3_PRIME | chr18 | 14837686 | |||||
| chr18:14837866
|
T | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(178): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.2988+190T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14837866 | ||||||
| chr18:14838010
|
C | T | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2988+334C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14838010 | ||||||
| chr18:14838093
|
A | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(74): Show | 80 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.2988+417A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14838093 | ||||||
| chr18:14838180
|
G | C | 15 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(12): Show | 15 | HG01167.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2988+504G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14838180 | ||||||
| chr18:14838272
|
G | GTA | 4 | a0001c0001t0001g0256a0001c0003t0001g0186a0001c0041t0001g0249others(1): Show | 4 | HG00642.hp2 HG01106.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2988+600_2988+601d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | INFO_REALIGN_3_PRIME | chr18 | 14838272 | |||||
| chr18:14838476
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(155): Show | 161 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2988+800T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14838476 | ||||||
| chr18:14838910
|
A | G | 66 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0015others(63): Show | 66 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.2988+1234A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14838910 | ||||||
| chr18:14839033
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2988+1357T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14839033 | ||||||
| chr18:14839121
|
C | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2988+1445C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14839121 | ||||||
| chr18:14839168
|
T | C | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2989-1420T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14839168 | ||||||
| chr18:14839822
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2989-766C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14839822 | ||||||
| chr18:14840051
|
C | T | 1 | a0001c0003t0004g0295 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2989-537C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14840051 | ||||||
| chr18:14840067
|
A | T | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2989-521A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14840067 | ||||||
| chr18:14840450
|
A | C | 1 | a0002c0002t0001g0144 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2989-138A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14840450 | ||||||
| chr18:14840513
|
C | T | 1 | a0002c0002t0001g0210 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2989-75C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14840513 | ||||||
| chr18:14840514
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2989-74G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | chr18 | 14840514 | ||||||
| chr18:14840550
|
T | TA | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2989-31dupA | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 36/43 | INFO_REALIGN_3_PRIME | chr18 | 14840550 | |||||
| chr18:14840888
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3079+210A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14840888 | ||||||
| chr18:14840958
|
G | A | 5 | a0006c0008t0001g0163a0006c0008t0001g0171a0006c0008t0001g0190others(2): Show | 5 | HG01891.hp2 HG01952.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3079+280G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14840958 | ||||||
| chr18:14841060
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3079+382A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14841060 | ||||||
| chr18:14841172
|
A | G | 1 | a0003c0006t0001g0240 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3079+494A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14841172 | ||||||
| chr18:14841280
|
A | G | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(4): Show | 7 | NA18950.hp2 NA18964.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3079+602A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14841280 | ||||||
| chr18:14841364
|
TG | T | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3079+687delG | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14841364 | ||||||
| chr18:14841377
|
T | G | 1 | a0002c0004t0001g0288 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3079+699T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14841377 | ||||||
| chr18:14841697
|
C | T | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3079+1019C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14841697 | ||||||
| chr18:14841751
|
T | G | 81 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0015others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3079+1073T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14841751 | ||||||
| chr18:14841965
|
T | A | 2 | a0008c0010t0001g0262a0008c0010t0008g0006 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3080-932T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14841965 | ||||||
| chr18:14842531
|
G | A | 115 | a0001c0055t0001g0088a0002c0002t0001g0098a0002c0002t0001g0107others(112): Show | 116 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.3080-366G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14842531 | ||||||
| chr18:14842532
|
T | G | 3 | a0006c0008t0001g0190a0006c0008t0001g0219a0013c0017t0005g0101 | 3 | HG01891.hp2 HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3080-365T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14842532 | ||||||
| chr18:14842537
|
T | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.3080-360T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14842537 | ||||||
| chr18:14842737
|
G | T | 1 | a0001c0001t0002g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3080-160G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14842737 | ||||||
| chr18:14842747
|
TAAAGAAA others(7): Show |
T | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3080-142_3080-129d others(16): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | INFO_REALIGN_3_PRIME | chr18 | 14842747 | |||||
| chr18:14842879
|
A | C | 1 | a0042c0052t0001g0079 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3080-18A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 37/43 | chr18 | 14842879 | ||||||
| chr18:14842960
|
A | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3108+35A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 38/43 | chr18 | 14842960 | ||||||
| chr18:14843195
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3181+99A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14843195 | ||||||
| chr18:14843317
|
G | A | 7 | a0003c0006t0001g0003a0003c0006t0001g0237a0003c0006t0001g0240others(4): Show | 8 | HG02055.hp1 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.3181+221G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14843317 | ||||||
| chr18:14843341
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(75): Show | 81 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.3181+245T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14843341 | ||||||
| chr18:14843553
|
C | CTG | 4 | a0002c0004t0001g0004a0004c0022t0001g0301a0010c0049t0001g0053others(1): Show | 5 | HG02572.hp2 HG03471.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.3181+496_3181+497d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
C | CTGTG | 16 | a0002c0002t0001g0098a0002c0002t0001g0107a0002c0002t0001g0141others(13): Show | 17 | HG00438.hp1 HG00621.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.3181+494_3181+497d others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
C | CTGTGTG | 27 | a0002c0002t0001g0116a0002c0002t0001g0130a0002c0002t0001g0142others(24): Show | 27 | HG01496.hp1 HG01517.hp1 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.3181+492_3181+497d others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
C | CTGTGTGT others(1): Show |
40 | a0002c0002t0001g0109a0002c0002t0001g0115a0002c0002t0001g0117others(37): Show | 40 | HG00323.hp1 HG00609.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.3181+490_3181+497d others(10): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
C | CTGTGTGT others(3): Show |
29 | a0001c0055t0001g0088a0002c0002t0001g0119a0002c0002t0001g0136others(26): Show | 29 | HG00099.hp1 HG00423.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.3181+488_3181+497d others(12): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
C | CTGTGTGT others(5): Show |
15 | a0002c0002t0001g0118a0002c0002t0001g0132a0002c0002t0001g0133others(12): Show | 15 | HG00544.hp1 HG00738.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.3181+486_3181+497d others(14): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
C | CTGTGTGT others(11): Show |
1 | a0002c0004t0001g0266 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3181+480_3181+497d others(20): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
CTG | C | 9 | a0002c0002t0001g0160a0003c0006t0001g0003a0003c0006t0001g0237others(6): Show | 10 | HG02055.hp1 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.3181+496_3181+497d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
CTGTG | C | 7 | a0001c0001t0002g0110a0001c0003t0002g0106a0001c0003t0002g0111others(4): Show | 7 | HG01074.hp2 HG01109.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.3181+494_3181+497d others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
CTGTGTG | C | 11 | a0001c0001t0002g0054a0001c0001t0004g0290a0001c0001t0004g0291others(8): Show | 11 | HG00544.hp2 HG01257.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.3181+492_3181+497d others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
CTGTGTGT others(1): Show |
C | 78 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0030others(75): Show | 80 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3181+490_3181+497d others(10): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
CTGTGTGT others(3): Show |
C | 67 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0023others(64): Show | 68 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.3181+488_3181+497d others(12): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14843553
|
CTGTGTGT others(5): Show |
C | 2 | a0001c0003t0009g0228a0001c0003t0009g0229 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3181+486_3181+497d others(14): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14843553 | |||||
| chr18:14844152
|
T | C | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3181+1056T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14844152 | ||||||
| chr18:14844254
|
G | C | 1 | a0001c0001t0004g0291 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3181+1158G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14844254 | ||||||
| chr18:14844381
|
T | A | 1 | a0039c0056t0001g0257 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3181+1285T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14844381 | ||||||
| chr18:14844545
|
T | C | 1 | a0008c0010t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3181+1449T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14844545 | ||||||
| chr18:14844550
|
G | A | 7 | a0003c0006t0001g0003a0003c0006t0001g0237a0003c0006t0001g0240others(4): Show | 8 | HG02055.hp1 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.3181+1454G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14844550 | ||||||
| chr18:14844552
|
G | A | 1 | a0003c0019t0001g0091 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3181+1456G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14844552 | ||||||
| chr18:14844792
|
G | A | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3181+1696G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14844792 | ||||||
| chr18:14844946
|
T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(73): Show | 79 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.3181+1850T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14844946 | ||||||
| chr18:14845123
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3181+2027C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14845123 | ||||||
| chr18:14845316
|
C | A | 1 | a0002c0002t0001g0248 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3181+2220C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14845316 | ||||||
| chr18:14845457
|
A | G | 2 | a0006c0008t0001g0163a0006c0008t0001g0171 | 2 | HG01952.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3181+2361A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14845457 | ||||||
| chr18:14845527
|
A | G | 6 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(3): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3181+2431A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14845527 | ||||||
| chr18:14845586
|
T | TTTTATTG others(27): Show |
1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3181+2491_3181+252 others(38): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14845586 | |||||
| chr18:14845778
|
A | G | 8 | a0001c0001t0003g0251a0001c0001t0003g0282a0001c0001t0003g0283others(5): Show | 8 | HG00609.hp1 HG02027.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.3181+2682A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14845778 | ||||||
| chr18:14846055
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(162): Show | 168 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.3182-2661G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14846055 | ||||||
| chr18:14846068
|
AT | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0027others(235): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.3182-2633delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14846068 | |||||
| chr18:14846068
|
ATT | A | 41 | a0001c0001t0001g0256a0001c0001t0002g0276a0001c0001t0003g0055others(38): Show | 41 | HG00609.hp1 HG00735.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.3182-2634_3182-263 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14846068 | |||||
| chr18:14846391
|
T | A | 1 | a0001c0011t0003g0223 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3182-2325T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14846391 | ||||||
| chr18:14846566
|
TTCTA | T | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3182-2144_3182-214 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14846566 | |||||
| chr18:14846754
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3182-1962T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14846754 | ||||||
| chr18:14846768
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3182-1948G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14846768 | ||||||
| chr18:14846948
|
T | TCCACCCC others(44): Show |
1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3182-1767_3182-176 others(55): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14846948 | |||||
| chr18:14846950
|
A | C | 1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3182-1766A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14846950 | ||||||
| chr18:14846953
|
A | C | 1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3182-1763A>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14846953 | ||||||
| chr18:14846954
|
TGCTGTTT others(101): Show |
T | 1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3182-1761_3182-165 others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14846954 | ||||||
| chr18:14847050
|
T | G | 1 | a0002c0002t0001g0231 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3182-1666T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847050 | ||||||
| chr18:14847050
|
T | TTA | 23 | a0002c0002t0001g0158a0002c0002t0001g0164a0002c0002t0001g0166others(20): Show | 23 | HG00438.hp1 HG01081.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.3182-1624_3182-162 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847050
|
T | TTATA | 22 | a0001c0055t0001g0088a0002c0002t0001g0115a0002c0002t0001g0118others(19): Show | 23 | HG00642.hp1 HG01255.hp1 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.3182-1626_3182-162 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847050
|
T | TTATATA | 8 | a0002c0002t0001g0138a0002c0002t0001g0143a0002c0002t0001g0177others(5): Show | 8 | HG00423.hp2 HG00609.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.3182-1628_3182-162 others(10): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847050
|
T | TTATATAT others(3): Show |
1 | a0002c0002t0001g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3182-1632_3182-162 others(14): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847050
|
TTA | T | 26 | a0002c0002t0001g0107a0002c0002t0001g0119a0002c0002t0001g0133others(23): Show | 26 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.3182-1624_3182-162 others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847050
|
TTATA | T | 6 | a0002c0002t0001g0098a0002c0004t0001g0278a0006c0008t0001g0190others(3): Show | 6 | HG00323.hp1 HG01891.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.3182-1626_3182-162 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847050
|
TTATATA | T | 4 | a0002c0002t0001g0132a0002c0002t0001g0208a0004c0022t0001g0301others(1): Show | 4 | HG02074.hp1 HG02572.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.3182-1628_3182-162 others(10): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847050
|
TTATATAT others(3): Show |
T | 8 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.3182-1632_3182-162 others(14): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847050
|
TTATATAT others(9): Show |
T | 9 | a0003c0006t0001g0003a0003c0006t0001g0237a0003c0006t0001g0240others(6): Show | 10 | HG02055.hp1 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.3182-1638_3182-162 others(20): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847050
|
TTATATAT others(11): Show |
T | 2 | a0009c0013t0005g0104a0009c0013t0005g0105 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3182-1640_3182-162 others(22): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847050
|
TTATATAT others(19): Show |
T | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(154): Show | 160 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.3182-1648_3182-162 others(30): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847050 | |||||
| chr18:14847052
|
A | T | 1 | a0004c0007t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3182-1664A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847052 | ||||||
| chr18:14847054
|
A | T | 2 | a0004c0007t0001g0309a0004c0007t0001g0310 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3182-1662A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847054 | ||||||
| chr18:14847058
|
A | T | 1 | a0004c0022t0001g0301 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3182-1658A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847058 | ||||||
| chr18:14847063
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3182-1653T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847063 | ||||||
| chr18:14847067
|
T | A | 1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3182-1649T>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847067 | ||||||
| chr18:14847070
|
A | T | 1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3182-1646A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847070 | ||||||
| chr18:14847073
|
T | G | 1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3182-1643T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847073 | ||||||
| chr18:14847074
|
A | T | 1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3182-1642A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847074 | ||||||
| chr18:14847076
|
A | T | 1 | a0001c0001t0001g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3182-1640A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847076 | ||||||
| chr18:14847093
|
T | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(175): Show | 182 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.3182-1623T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847093 | ||||||
| chr18:14847182
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3182-1534G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847182 | ||||||
| chr18:14847230
|
G | A | 2 | a0009c0013t0005g0104a0009c0013t0005g0105 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3182-1486G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847230 | ||||||
| chr18:14847292
|
A | T | 1 | a0001c0001t0002g0046 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3182-1424A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847292 | ||||||
| chr18:14847305
|
A | G | 1 | a0034c0053t0010g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3182-1411A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847305 | ||||||
| chr18:14847511
|
G | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(178): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.3182-1205G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847511 | ||||||
| chr18:14847512
|
CATAG | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(178): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.3182-1201_3182-119 others(8): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14847512 | |||||
| chr18:14847663
|
G | A | 1 | a0002c0002t0001g0225 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3182-1053G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847663 | ||||||
| chr18:14847771
|
G | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(162): Show | 168 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.3182-945G>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847771 | ||||||
| chr18:14847890
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(162): Show | 168 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.3182-826T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14847890 | ||||||
| chr18:14848065
|
G | A | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3182-651G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14848065 | ||||||
| chr18:14848333
|
C | T | 1 | a0001c0001t0003g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3182-383C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14848333 | ||||||
| chr18:14848359
|
C | G | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3182-357C>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14848359 | ||||||
| chr18:14848415
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(162): Show | 168 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.3182-301C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14848415 | ||||||
| chr18:14848428
|
C | T | 4 | a0008c0010t0001g0262a0008c0010t0008g0006a0008c0010t0008g0007others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3182-288C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14848428 | ||||||
| chr18:14848429
|
G | A | 114 | a0001c0055t0001g0088a0002c0002t0001g0098a0002c0002t0001g0107others(111): Show | 115 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.3182-287G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14848429 | ||||||
| chr18:14848550
|
GT | G | 6 | a0001c0001t0002g0048a0001c0001t0002g0276a0009c0013t0005g0100others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.3182-155delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | INFO_REALIGN_3_PRIME | chr18 | 14848550 | |||||
| chr18:14848585
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3182-131A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 39/43 | chr18 | 14848585 | ||||||
| chr18:14848936
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(162): Show | 168 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
splice_region_variant&intron_variant | LOW | c.3395+7C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14848936 | ||||||
| chr18:14849311
|
A | T | 1 | a0002c0002t0001g0173 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3395+382A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849311 | ||||||
| chr18:14849321
|
A | AG | 10 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(7): Show | 10 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3395+392_3395+393i others(3): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849321 | ||||||
| chr18:14849359
|
T | C | 13 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(10): Show | 13 | HG00621.hp1 HG02132.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.3395+430T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849359 | ||||||
| chr18:14849408
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(162): Show | 168 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.3395+479C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849408 | ||||||
| chr18:14849410
|
G | C | 1 | a0017c0016t0003g0148 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3395+481G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849410 | ||||||
| chr18:14849493
|
T | C | 5 | a0002c0002t0001g0132a0002c0002t0001g0137a0002c0002t0001g0140others(2): Show | 5 | NA18943.hp2 NA18951.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.3395+564T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849493 | ||||||
| chr18:14849560
|
T | G | 2 | a0006c0008t0001g0163a0006c0008t0001g0171 | 2 | HG01952.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3395+631T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849560 | ||||||
| chr18:14849589
|
T | G | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3396-625T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849589 | ||||||
| chr18:14849604
|
T | C | 10 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(7): Show | 10 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3396-610T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849604 | ||||||
| chr18:14849827
|
T | C | 1 | a0042c0052t0001g0079 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3396-387T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849827 | ||||||
| chr18:14849833
|
G | A | 1 | a0001c0003t0001g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3396-381G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849833 | ||||||
| chr18:14849876
|
C | T | 1 | a0008c0010t0001g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3396-338C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14849876 | ||||||
| chr18:14850056
|
T | C | 14 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0003t0004g0244others(11): Show | 14 | HG01167.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.3396-158T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 40/43 | chr18 | 14850056 | ||||||
| chr18:14850640
|
A | G | 1 | a0001c0003t0002g0155 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3564+258A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | chr18 | 14850640 | ||||||
| chr18:14850829
|
G | A | 10 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(7): Show | 10 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3564+447G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | chr18 | 14850829 | ||||||
| chr18:14851109
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(178): Show | 185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.3565-400T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | chr18 | 14851109 | ||||||
| chr18:14851234
|
A | T | 6 | a0001c0001t0003g0269a0001c0001t0003g0271a0001c0001t0003g0272others(3): Show | 6 | NA18945.hp1 NA18952.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.3565-275A>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | chr18 | 14851234 | ||||||
| chr18:14851237
|
G | GT | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(69): Show | 76 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.3565-258dupT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | INFO_REALIGN_3_PRIME | chr18 | 14851237 | |||||
| chr18:14851237
|
G | GTT | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(9): Show | 12 | HG00621.hp1 HG02132.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.3565-259_3565-258d others(4): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | INFO_REALIGN_3_PRIME | chr18 | 14851237 | |||||
| chr18:14851237
|
G | GTTTT | 6 | a0008c0010t0001g0261a0008c0010t0001g0262a0008c0010t0008g0006others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3565-261_3565-258d others(6): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | INFO_REALIGN_3_PRIME | chr18 | 14851237 | |||||
| chr18:14851240
|
T | G | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3565-269T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | chr18 | 14851240 | ||||||
| chr18:14851371
|
T | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(155): Show | 161 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.3565-138T>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | chr18 | 14851371 | ||||||
| chr18:14851373
|
C | T | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3565-136C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | chr18 | 14851373 | ||||||
| chr18:14851465
|
C | T | 1 | a0028c0025t0001g0202 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3565-44C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 41/43 | chr18 | 14851465 | ||||||
| chr18:14852497
|
A | AAT | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.4476+91_4476+92dup others(2): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | INFO_REALIGN_3_PRIME | chr18 | 14852497 | |||||
| chr18:14852503
|
T | C | 5 | a0004c0007t0001g0005a0004c0007t0001g0299a0004c0007t0001g0309others(2): Show | 6 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.4476+83T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14852503 | ||||||
| chr18:14852591
|
C | T | 1 | a0002c0004t0001g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4476+171C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14852591 | ||||||
| chr18:14852778
|
G | C | 2 | a0002c0002t0001g0199a0002c0002t0001g0200 | 2 | NA18981.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.4476+358G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14852778 | ||||||
| chr18:14852879
|
A | ATTTATTC others(27): Show |
1 | a0001c0003t0002g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4476+462_4476+463i others(36): Show |
ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | INFO_REALIGN_3_PRIME | chr18 | 14852879 | |||||
| chr18:14852883
|
C | T | 1 | a0001c0003t0002g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4476+463C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14852883 | ||||||
| chr18:14853149
|
C | T | 1 | a0002c0002t0001g0178 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4477-660C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14853149 | ||||||
| chr18:14853213
|
T | C | 1 | a0003c0021t0001g0239 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4477-596T>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14853213 | ||||||
| chr18:14853418
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4477-391A>G | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14853418 | ||||||
| chr18:14853535
|
C | CT | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(153): Show | 159 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.4477-260dupT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | INFO_REALIGN_3_PRIME | chr18 | 14853535 | |||||
| chr18:14853557
|
C | A | 1 | a0001c0001t0003g0281 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4477-252C>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14853557 | ||||||
| chr18:14853697
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(166): Show | 172 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.4477-112G>A | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14853697 | ||||||
| chr18:14853702
|
C | T | 1 | a0002c0004t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4477-107C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14853702 | ||||||
| chr18:14853801
|
C | T | 7 | a0007c0009t0007g0128a0007c0009t0007g0129a0007c0009t0007g0226others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.4477-8C>T | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 42/43 | chr18 | 14853801 | ||||||
| chr18:14853971
|
G | C | 4 | a0009c0013t0005g0100a0009c0013t0005g0104a0009c0013t0005g0105others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.*33+28G>C | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 43/43 | chr18 | 14853971 | ||||||
| chr18:14854178
|
CT | C | 9 | a0001c0001t0002g0069a0004c0022t0001g0301a0004c0045t0010g0089others(6): Show | 9 | HG01243.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.*34-4delT | ANKRD30B | ENSG00000180777.15 | transcript | ENST00000690538.1 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr18 | 14854178 |