Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23243 |
|---|---|
| ensemblid | ENSG00000206560.12 |
| hgncid | 29024 |
| symbol | ANKRD28 |
| name | ankyrin repeat domain 28 |
| refseq_nuc | NM_001349278.2 |
| refseq_prot | NP_001336207.1 |
| ensembl_nuc | ENST00000683139.1 |
| ensembl_prot | ENSP00000508086.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 15667236 |
| end | 15797979 |
| strand | - |
| ver | v1.2 |
| region | chr3:15667236-15797979 |
| region5000 | chr3:15662236-15802979 |
| regionname0 | ANKRD28_chr3_15667236_15797979 |
| regionname5000 | ANKRD28_chr3_15662236_15802979 |
| 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 | 1/1 | 1083 | 329 | 91 | 55 | 139 | 10 | 32 | 105 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0002 | 0/0 | 1083 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0003 | 0/0 | 1083 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0004 | 0/0 | 1083 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0005 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0006 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0007 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| 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 | 1/0 | 3252 | 166 | 45 | 23 | 75 | 3 | 19 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0002 | 0/1 | 3252 | 124 | 12 | 30 | 61 | 7 | 13 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0003 | 0/0 | 3252 | 15 | 13 | 2 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0004 | 0/0 | 3252 | 9 | 9 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0005 | 0/0 | 3252 | 6 | 6 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0006 | 0/0 | 3252 | 4 | 0 | 2 | 0 | 0 | 2 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0007 | 0/0 | 3252 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0008 | 0/0 | 3252 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0009 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0010 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0011 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0012 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0013 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0014 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0015 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0016 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| c0017 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| 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 | 0/1 | 4494 | 99 | 11 | 23 | 44 | 7 | 13 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0002 | 0/0 | 4491 | 87 | 15 | 8 | 58 | 0 | 6 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0003 | 1/0 | 4493 | 21 | 3 | 6 | 7 | 1 | 3 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0004 | 0/0 | 4494 | 15 | 9 | 2 | 0 | 0 | 4 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0005 | 0/0 | 4493 | 12 | 10 | 2 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0006 | 0/0 | 4493 | 11 | 8 | 3 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0007 | 0/0 | 4494 | 8 | 0 | 0 | 8 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0008 | 0/0 | 4493 | 8 | 5 | 0 | 3 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0009 | 0/0 | 4491 | 6 | 6 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0010 | 0/0 | 4493 | 5 | 4 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0011 | 0/0 | 4495 | 4 | 0 | 3 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0012 | 0/0 | 4493 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0013 | 0/0 | 4490 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0014 | 0/0 | 4494 | 3 | 0 | 3 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0015 | 0/0 | 4493 | 3 | 0 | 0 | 0 | 0 | 3 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0016 | 0/0 | 4493 | 3 | 0 | 2 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0017 | 0/0 | 4492 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0018 | 0/0 | 4493 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0019 | 0/0 | 4492 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0020 | 0/0 | 4492 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0021 | 0/0 | 4493 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0022 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0023 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0024 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0025 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0026 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0027 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0028 | 0/0 | 4491 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0029 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0030 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0031 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0032 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0033 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0034 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0035 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0036 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0037 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0038 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0039 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0040 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0041 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0042 | 0/0 | 4495 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0043 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0044 | 0/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0045 | 0/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0046 | 0/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0047 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0048 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0049 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0050 | 0/0 | 4495 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0051 | 0/0 | 4495 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0052 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0053 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0054 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0055 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0056 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0057 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0058 | 0/0 | 4493 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| t0059 | 0/0 | 4492 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| 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 | 1/0 | 3252 | 166 | 45 | 23 | 75 | 3 | 19 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002 | 0/1 | 3252 | 124 | 12 | 30 | 61 | 7 | 13 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0003 | 0/0 | 3252 | 15 | 13 | 2 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0004 | 0/0 | 3252 | 9 | 9 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0005 | 0/0 | 3252 | 6 | 6 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0007 | 0/0 | 3252 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0009 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0010 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0014 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0017 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0002c0006 | 0/0 | 3252 | 4 | 0 | 2 | 0 | 0 | 2 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0003c0013 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0003c0015 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0004c0008 | 0/0 | 3252 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0005c0011 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0006c0012 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0007c0016 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0002 | 0/0 | 7742 | 85 | 15 | 8 | 56 | 0 | 6 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0003 | 1/0 | 7744 | 20 | 3 | 6 | 6 | 1 | 3 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0004 | 0/0 | 7745 | 14 | 8 | 2 | 0 | 0 | 4 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0006 | 0/0 | 7744 | 10 | 7 | 3 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0008 | 0/0 | 7744 | 8 | 5 | 0 | 3 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0010 | 0/0 | 7744 | 5 | 4 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0013 | 0/0 | 7741 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0015 | 0/0 | 7744 | 3 | 0 | 0 | 0 | 0 | 3 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0016 | 0/0 | 7744 | 3 | 0 | 2 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0023 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0024 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0026 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0027 | 0/0 | 7742 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0028 | 0/0 | 7742 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0029 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0032 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0033 | 0/0 | 7743 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0034 | 0/0 | 7743 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0039 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0044 | 0/0 | 7745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0056 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0058 | 0/0 | 7744 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0001t0059 | 0/0 | 7743 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0001 | 0/1 | 7745 | 94 | 11 | 21 | 44 | 7 | 10 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0007 | 0/0 | 7745 | 8 | 0 | 0 | 8 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0011 | 0/0 | 7746 | 3 | 0 | 2 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0014 | 0/0 | 7745 | 3 | 0 | 3 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0017 | 0/0 | 7743 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0022 | 0/0 | 7745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0030 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0038 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0040 | 0/0 | 7745 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0041 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0042 | 0/0 | 7746 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0043 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0045 | 0/0 | 7745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0046 | 0/0 | 7745 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0047 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0048 | 0/0 | 7744 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0049 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0051 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0002t0055 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0003t0005 | 0/0 | 7744 | 10 | 8 | 2 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0003t0018 | 0/0 | 7744 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0003t0019 | 0/0 | 7743 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0003t0053 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0004t0009 | 0/0 | 7742 | 6 | 6 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0004t0025 | 0/0 | 7742 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0004t0035 | 0/0 | 7742 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0004t0054 | 0/0 | 7743 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0005t0012 | 0/0 | 7744 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0005t0020 | 0/0 | 7743 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0005t0036 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0005t0057 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0007t0021 | 0/0 | 7744 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0007t0031 | 0/0 | 7742 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0009t0005 | 0/0 | 7744 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0010t0012 | 0/0 | 7744 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0014t0037 | 0/0 | 7745 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0001c0017t0004 | 0/0 | 7745 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0002c0006t0001 | 0/0 | 7745 | 4 | 0 | 2 | 0 | 0 | 2 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0003c0013t0052 | 0/0 | 7745 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0003c0015t0011 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0004c0008t0002 | 0/0 | 7742 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0005c0011t0003 | 0/0 | 7744 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0006c0012t0006 | 0/0 | 7744 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| a0007c0016t0050 | 0/0 | 7746 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | copy fasta | chr3 | 15662236 | 15802979 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0006g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0006g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0006g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0006g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0006g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0008g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0008g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0008g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0008g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0008g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0008g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0008g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0010g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0010g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0010g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0010g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0013g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0013g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0015g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0015g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0015g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0016g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0016g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0016g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0023g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0024g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0026g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0027g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0028g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0029g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0032g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0033g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0034g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0039g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0044g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0056g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0058g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0001t0059g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0011g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0011g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0011g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0014g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0014g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0014g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0017g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0017g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0022g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0030g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0038g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0040g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0041g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0042g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0043g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0045g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0046g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0047g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0048g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0049g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0051g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0002t0055g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0005g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0018g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0018g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0019g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0019g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0003t0053g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0004t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0004t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0004t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0004t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0004t0009g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0004t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0004t0025g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0004t0035g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0004t0054g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0005t0012g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0005t0012g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0005t0020g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0005t0020g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0005t0036g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0005t0057g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0007t0021g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0007t0021g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0007t0031g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0009t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0009t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0010t0012g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0010t0012g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0014t0037g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0001c0017t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0002c0006t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0002c0006t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0002c0006t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0002c0006t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0003c0013t0052g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0003c0015t0011g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0004c0008t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0004c0008t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0005c0011t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0006c0012t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| a0007c0016t0050g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0269 | EUR | GBR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0199 | EUR | GBR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00140 | hp1 | a0001 | c0001 | t0016 | g0327 | EUR | GBR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0221 | EUR | GBR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00597 | hp1 | a0001 | c0002 | t0017 | g0227 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00639 | hp2 | a0001 | c0002 | t0022 | g0002 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00642 | hp1 | a0002 | c0006 | t0001 | g0135 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0205 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00738 | hp2 | a0001 | c0002 | t0014 | g0110 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01099 | hp2 | a0001 | c0002 | t0051 | g0279 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01109 | hp1 | a0002 | c0006 | t0001 | g0207 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01109 | hp2 | a0001 | c0003 | t0005 | g0282 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0312 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01168 | hp2 | a0001 | c0003 | t0005 | g0286 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0311 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0247 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01192 | hp1 | a0001 | c0002 | t0014 | g0111 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0309 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01255 | hp1 | a0001 | c0002 | t0011 | g0237 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01255 | hp2 | a0001 | c0002 | t0040 | g0108 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0220 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01261 | hp2 | a0001 | c0001 | t0016 | g0328 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01433 | hp1 | a0001 | c0001 | t0016 | g0330 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01433 | hp2 | a0001 | c0001 | t0028 | g0008 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0216 | EUR | IBS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01515 | hp2 | a0001 | c0001 | t0058 | g0329 | EUR | IBS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0217 | EUR | IBS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0136 | EUR | IBS | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0305 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01884 | hp2 | a0003 | c0013 | t0052 | g0293 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01934 | hp2 | a0001 | c0001 | t0010 | g0274 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01981 | hp1 | a0001 | c0002 | t0014 | g0109 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01993 | hp2 | a0003 | c0015 | t0011 | g0234 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02004 | hp2 | a0001 | c0002 | t0011 | g0236 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02055 | hp1 | a0001 | c0003 | t0005 | g0289 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0275 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02071 | hp1 | a0001 | c0001 | t0008 | g0338 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02083 | hp1 | a0001 | c0002 | t0038 | g0106 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02145 | hp2 | a0001 | c0005 | t0020 | g0300 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CDX | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | CDX | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CDX | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | CDX | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02257 | hp1 | a0001 | c0004 | t0009 | g0296 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02258 | hp1 | a0001 | c0004 | t0009 | g0294 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0304 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02280 | hp2 | a0001 | c0003 | t0005 | g0291 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02300 | hp1 | a0001 | c0002 | t0048 | g0226 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02602 | hp1 | a0001 | c0002 | t0042 | g0133 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0246 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02615 | hp1 | a0001 | c0004 | t0009 | g0295 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02622 | hp1 | a0001 | c0010 | t0012 | g0316 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02630 | hp1 | a0001 | c0001 | t0039 | g0107 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02647 | hp1 | a0001 | c0003 | t0005 | g0287 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02647 | hp2 | a0001 | c0005 | t0036 | g0104 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02683 | hp2 | a0001 | c0001 | t0015 | g0326 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02717 | hp1 | a0001 | c0003 | t0005 | g0281 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0306 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0308 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02723 | hp2 | a0001 | c0004 | t0025 | g0005 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02809 | hp2 | a0001 | c0003 | t0005 | g0288 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02895 | hp1 | a0001 | c0001 | t0027 | g0007 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02896 | hp1 | a0001 | c0009 | t0005 | g0284 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0336 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02897 | hp2 | a0001 | c0009 | t0005 | g0283 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02922 | hp1 | a0001 | c0003 | t0005 | g0285 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0307 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02965 | hp1 | a0001 | c0014 | t0037 | g0105 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0277 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0278 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0268 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03041 | hp1 | a0001 | c0004 | t0054 | g0320 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03041 | hp2 | a0001 | c0003 | t0005 | g0292 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03098 | hp1 | a0001 | c0004 | t0009 | g0299 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03098 | hp2 | a0001 | c0005 | t0020 | g0301 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0337 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03130 | hp2 | a0001 | c0003 | t0018 | g0232 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03139 | hp2 | a0001 | c0004 | t0009 | g0298 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03195 | hp2 | a0001 | c0003 | t0018 | g0233 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03209 | hp1 | a0001 | c0005 | t0012 | g0318 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03209 | hp2 | a0001 | c0003 | t0019 | g0230 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03225 | hp1 | a0001 | c0005 | t0057 | g0323 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03486 | hp1 | a0001 | c0001 | t0056 | g0322 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03486 | hp2 | a0007 | c0016 | t0050 | g0280 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0222 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0332 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03516 | hp2 | a0001 | c0003 | t0053 | g0313 | AFR | ESN | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0249 | AFR | GWD | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0242 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0270 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0239 | SAS | PJL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0213 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03831 | hp2 | a0001 | c0001 | t0059 | g0333 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0238 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03927 | hp1 | a0001 | c0002 | t0046 | g0153 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0245 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03942 | hp2 | a0001 | c0001 | t0015 | g0324 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0261 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG04115 | hp2 | a0002 | c0006 | t0001 | g0202 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0156 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG04184 | hp2 | a0001 | c0001 | t0015 | g0325 | SAS | BEB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG04204 | hp1 | a0001 | c0002 | t0045 | g0161 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG04228 | hp1 | a0002 | c0006 | t0001 | g0203 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | STU | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18522 | hp1 | a0001 | c0003 | t0019 | g0231 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0314 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18747 | hp2 | a0001 | c0002 | t0049 | g0229 | EAS | CHB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0335 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18944 | hp2 | a0001 | c0002 | t0007 | g0179 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18945 | hp1 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18950 | hp1 | a0001 | c0002 | t0007 | g0175 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18954 | hp2 | a0001 | c0001 | t0029 | g0009 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18956 | hp1 | a0001 | c0002 | t0017 | g0228 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18956 | hp2 | a0001 | c0001 | t0008 | g0339 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18957 | hp1 | a0001 | c0007 | t0031 | g0049 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18961 | hp2 | a0005 | c0011 | t0003 | g0255 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18967 | hp1 | a0001 | c0002 | t0011 | g0235 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18967 | hp2 | a0001 | c0001 | t0026 | g0006 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18969 | hp1 | a0001 | c0001 | t0023 | g0003 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18970 | hp2 | a0001 | c0002 | t0055 | g0321 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0334 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18977 | hp2 | a0001 | c0001 | t0013 | g0028 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18980 | hp1 | a0001 | c0001 | t0033 | g0101 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18983 | hp1 | a0001 | c0002 | t0007 | g0182 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18985 | hp1 | a0001 | c0002 | t0007 | g0187 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18991 | hp1 | a0001 | c0002 | t0041 | g0169 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19003 | hp2 | a0001 | c0002 | t0007 | g0174 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19007 | hp1 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19011 | hp1 | a0001 | c0002 | t0007 | g0176 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0331 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19043 | hp2 | a0001 | c0005 | t0012 | g0319 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19054 | hp2 | a0001 | c0001 | t0032 | g0066 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19057 | hp2 | a0001 | c0002 | t0047 | g0189 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19058 | hp2 | a0001 | c0002 | t0007 | g0177 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19060 | hp2 | a0001 | c0002 | t0007 | g0184 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19068 | hp1 | a0001 | c0002 | t0043 | g0122 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19077 | hp1 | a0004 | c0008 | t0002 | g0043 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19077 | hp2 | a0004 | c0008 | t0002 | g0088 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19087 | hp1 | a0001 | c0007 | t0021 | g0302 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19089 | hp1 | a0001 | c0001 | t0034 | g0102 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19090 | hp1 | a0001 | c0007 | t0021 | g0303 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19091 | hp2 | a0001 | c0001 | t0024 | g0004 | EAS | JPT | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0276 | AFR | YRI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ASW | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | ASW | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0210 | EUR | TSI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0218 | EUR | TSI | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | GIH | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA20905 | hp2 | a0001 | c0001 | t0044 | g0178 | SAS | GIH | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | CLM | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02109 | hp1 | a0006 | c0012 | t0006 | g0310 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02486 | hp1 | a0001 | c0017 | t0004 | g0250 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02559 | hp1 | a0001 | c0004 | t0035 | g0103 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0315 | AFR | ACB | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03471 | hp1 | a0001 | c0010 | t0012 | g0317 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG03471 | hp2 | a0001 | c0003 | t0005 | g0290 | AFR | MSL | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG06807 | hp1 | a0001 | c0004 | t0009 | g0297 | AFR | USA | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | USA | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0243 | AFR | USA | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | USA | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| NA21309 | hp2 | a0001 | c0002 | t0030 | g0010 | AFR | LWK | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0212 | REF | REF | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0267 | REF | REF | ANKRD28_chr3_15662236_15802979 | ANKRD28 | chr3 | 15662236 | 15802979 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15677542
|
T | C | 1 | a0002 | 4 | HG00642.hp1 HG01109.hp1 HG04115.hp2 others(1): Show |
missense_variant | MODERATE | c.2728A>G | p.Ser910Gly | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 25/28 | 4186/7744 | 2728/3252 | 910/1083 | chr3 | 15677542 | ||
| chr3:15679512
|
G | A | 1 | a0003 | 2 | HG01884.hp2 HG01993.hp2 |
missense_variant | MODERATE | c.2441C>T | p.Thr814Met | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 22/28 | 3899/7744 | 2441/3252 | 814/1083 | chr3 | 15679512 | ||
| chr3:15707993
|
C | G | 1 | a0006 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1478G>C | p.Ser493Thr | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/28 | 2936/7744 | 1478/3252 | 493/1083 | chr3 | 15707993 | ||
| chr3:15713537
|
C | T | 1 | a0004 | 2 | NA19077.hp1 NA19077.hp2 |
missense_variant | MODERATE | c.1180G>A | p.Asp394Asn | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/28 | 2638/7744 | 1180/3252 | 394/1083 | chr3 | 15713537 | ||
| chr3:15721027
|
A | G | 1 | a0005 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.884T>C | p.Val295Ala | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/28 | 2342/7744 | 884/3252 | 295/1083 | chr3 | 15721027 | ||
| chr3:15737037
|
C | A | 1 | a0007 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.548G>T | p.Gly183Val | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/28 | 2006/7744 | 548/3252 | 183/1083 | chr3 | 15737037 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15675914
|
A | C | 1 | a0001c0007 | 3 | NA18957.hp1 NA19087.hp1 NA19090.hp1 |
synonymous_variant | LOW | c.2949T>G | p.Leu983Leu | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/28 | 4407/7744 | 2949/3252 | 983/1083 | chr3 | 15675914 | ||
| chr3:15678311
|
A | G | 1 | a0001c0014 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2605T>C | p.Leu869Leu | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/28 | 4063/7744 | 2605/3252 | 869/1083 | chr3 | 15678311 | ||
| chr3:15679478
|
G | A | 1 | a0001c0009 | 2 | HG02896.hp1 HG02897.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2475C>T | p.Ala825Ala | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 22/28 | 3933/7744 | 2475/3252 | 825/1083 | chr3 | 15679478 | ||
| chr3:15686293
|
T | C | 1 | a0001c0010 | 2 | HG02622.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.1980A>G | p.Ser660Ser | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 19/28 | 3438/7744 | 1980/3252 | 660/1083 | chr3 | 15686293 | ||
| chr3:15690029
|
A | T | 3 | a0001c0003a0001c0004a0001c0009 | 26 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(23): Show |
synonymous_variant | LOW | c.1953T>A | p.Ile651Ile | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/28 | 3411/7744 | 1953/3252 | 651/1083 | chr3 | 15690029 | ||
| chr3:15696182
|
G | A | 9 | a0001c0002a0001c0003a0001c0005others(6): Show | 156 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(153): Show |
synonymous_variant | LOW | c.1611C>T | p.Asn537Asn | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/28 | 3069/7744 | 1611/3252 | 537/1083 | chr3 | 15696182 | ||
| chr3:15696191
|
T | C | 6 | a0001c0002a0001c0004a0001c0014others(3): Show | 140 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(137): Show |
synonymous_variant | LOW | c.1602A>G | p.Gln534Gln | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/28 | 3060/7744 | 1602/3252 | 534/1083 | chr3 | 15696191 | ||
| chr3:15766256
|
G | A | 1 | a0001c0017 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.258C>T | p.Ile86Ile | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/28 | 1716/7744 | 258/3252 | 86/1083 | chr3 | 15766256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15667296
|
A | G | 2 | a0001c0007t0021a0001c0007t0031 | 3 | NA18957.hp1 NA19087.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2974T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2974 | chr3 | 15667296 | |||||
| chr3:15667359
|
G | C | 2 | a0001c0003t0005a0001c0009t0005 | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2911C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2911 | chr3 | 15667359 | |||||
| chr3:15667633
|
G | A | 2 | a0001c0002t0014a0001c0002t0051 | 4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2637C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2637 | chr3 | 15667633 | |||||
| chr3:15667807
|
A | T | 1 | a0001c0002t0043 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2463T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2463 | chr3 | 15667807 | |||||
| chr3:15667919
|
T | C | 2 | a0001c0001t0006a0006c0012t0006 | 11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2351A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2351 | chr3 | 15667919 | |||||
| chr3:15667942
|
G | A | 1 | a0001c0001t0032 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2328C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2328 | chr3 | 15667942 | |||||
| chr3:15668031
|
T | C | 2 | a0001c0002t0030a0001c0014t0037 | 2 | HG02965.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2239A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 2239 | chr3 | 15668031 | |||||
| chr3:15668355
|
A | AT | 5 | a0001c0002t0042a0001c0003t0018a0001c0003t0019others(2): Show | 7 | HG01884.hp2 HG02602.hp1 HG03130.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1914dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1914 | chr3 | 15668355 | |||||
| chr3:15668355
|
AT | A | 6 | a0001c0001t0013a0001c0001t0059a0001c0004t0009others(3): Show | 13 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1914delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1914 | chr3 | 15668355 | |||||
| chr3:15668504
|
T | C | 27 | a0001c0001t0002a0001c0001t0006a0001c0001t0013others(24): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1766A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1766 | chr3 | 15668504 | |||||
| chr3:15668766
|
A | T | 2 | a0001c0002t0007a0001c0002t0047 | 9 | NA18944.hp2 NA18950.hp1 NA18983.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1504T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1504 | chr3 | 15668766 | |||||
| chr3:15669006
|
T | A | 1 | a0001c0005t0020 | 2 | HG02145.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1264A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1264 | chr3 | 15669006 | |||||
| chr3:15669163
|
C | T | 2 | a0001c0003t0005a0001c0009t0005 | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1107G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1107 | chr3 | 15669163 | |||||
| chr3:15669259
|
A | G | 1 | a0001c0002t0041 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1011T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 1011 | chr3 | 15669259 | |||||
| chr3:15669286
|
G | C | 1 | a0001c0001t0058 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*984C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 984 | chr3 | 15669286 | |||||
| chr3:15669716
|
C | T | 2 | a0001c0001t0010a0001c0001t0056 | 6 | HG01934.hp2 HG02055.hp2 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*554G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 554 | chr3 | 15669716 | |||||
| chr3:15669853
|
C | A | 1 | a0001c0002t0045 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 417 | chr3 | 15669853 | |||||
| chr3:15669884
|
CT | C | 2 | a0001c0003t0019a0001c0003t0053 | 3 | HG03209.hp2 HG03516.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 385 | chr3 | 15669884 | |||||
| chr3:15669937
|
T | C | 1 | a0001c0002t0046 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*333A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 333 | chr3 | 15669937 | |||||
| chr3:15670198
|
T | A | 1 | a0001c0002t0047 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*72A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 28/28 | 72 | chr3 | 15670198 | |||||
| chr3:15796643
|
G | GT | 5 | a0001c0001t0004a0001c0002t0030a0001c0002t0048others(2): Show | 18 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-123dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 123 | chr3 | 15796643 | |||||
| chr3:15796643
|
G | GTT | 21 | a0001c0001t0001a0001c0001t0044a0001c0002t0001others(18): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
5_prime_UTR_variant | MODIFIER | c.-124_-123dupAA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 123 | chr3 | 15796643 | |||||
| chr3:15796643
|
GT | G | 13 | a0001c0001t0002a0001c0001t0013a0001c0001t0023others(10): Show | 100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
5_prime_UTR_variant | MODIFIER | c.-123delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 123 | chr3 | 15796643 | |||||
| chr3:15796752
|
G | A | 1 | a0001c0002t0049 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-231C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 231 | chr3 | 15796752 | |||||
| chr3:15796808
|
A | C | 1 | a0001c0002t0040 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-287T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 287 | chr3 | 15796808 | |||||
| chr3:15796828
|
T | A | 4 | a0001c0003t0005a0001c0003t0018a0001c0003t0019others(1): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-307A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 307 | chr3 | 15796828 | |||||
| chr3:15796920
|
A | C | 1 | a0001c0001t0029 | 1 | NA18954.hp2 | 5_prime_UTR_variant | MODIFIER | c.-399T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 399 | chr3 | 15796920 | |||||
| chr3:15797051
|
T | C | 1 | a0001c0005t0036 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-530A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 530 | chr3 | 15797051 | |||||
| chr3:15797102
|
A | G | 1 | a0001c0005t0036 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-581T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 581 | chr3 | 15797102 | |||||
| chr3:15797203
|
C | A | 56 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(53): Show | 281 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(278): Show |
5_prime_UTR_variant | MODIFIER | c.-682G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 682 | chr3 | 15797203 | |||||
| chr3:15797204
|
A | C | 1 | a0001c0001t0028 | 1 | HG01433.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-683T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797204 | ||||||
| chr3:15797205
|
A | C | 1 | a0001c0001t0027 | 1 | HG02895.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-684T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797205 | ||||||
| chr3:15797209
|
C | A | 4 | a0001c0001t0033a0001c0002t0011a0001c0007t0021others(1): Show | 7 | HG01255.hp1 HG01993.hp2 HG02004.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-688G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 688 | chr3 | 15797209 | |||||
| chr3:15797209
|
CA | C | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(39): Show | 245 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(242): Show |
5_prime_UTR_variant | MODIFIER | c.-689delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 689 | chr3 | 15797209 | |||||
| chr3:15797210
|
A | C | 4 | a0001c0001t0033a0001c0002t0011a0001c0007t0021others(1): Show | 7 | HG01255.hp1 HG01993.hp2 HG02004.hp2 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-689T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797210 | ||||||
| chr3:15797213
|
A | C | 2 | a0001c0001t0026a0003c0013t0052 | 2 | HG01884.hp2 NA18967.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-692T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797213 | ||||||
| chr3:15797248
|
C | T | 1 | a0001c0001t0039 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-727G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 727 | chr3 | 15797248 | |||||
| chr3:15797254
|
G | A | 10 | a0001c0001t0006a0001c0003t0053a0001c0004t0009others(7): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-733C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797254 | ||||||
| chr3:15797558
|
T | A | 1 | a0001c0002t0055 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1037A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1037 | chr3 | 15797558 | |||||
| chr3:15797558
|
T | TA | 5 | a0001c0004t0054a0001c0005t0012a0001c0005t0036others(2): Show | 7 | HG02622.hp1 HG02647.hp2 HG03041.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-1038dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1038 | chr3 | 15797558 | |||||
| chr3:15797559
|
A | T | 1 | a0001c0002t0038 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1038T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1038 | chr3 | 15797559 | |||||
| chr3:15797564
|
A | G | 2 | a0001c0001t0016a0001c0001t0058 | 4 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-1043T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1043 | chr3 | 15797564 | |||||
| chr3:15797569
|
A | G | 3 | a0001c0001t0015a0001c0002t0022a0001c0014t0037 | 5 | HG00639.hp2 HG02683.hp2 HG02965.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-1048T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1048 | chr3 | 15797569 | |||||
| chr3:15797578
|
A | G | 17 | a0001c0001t0002a0001c0001t0013a0001c0001t0023others(14): Show | 104 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
5_prime_UTR_variant | MODIFIER | c.-1057T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1057 | chr3 | 15797578 | |||||
| chr3:15797579
|
A | G | 2 | a0001c0001t0024a0001c0004t0025 | 2 | HG02723.hp2 NA19091.hp2 |
5_prime_UTR_variant | MODIFIER | c.-1058T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1058 | chr3 | 15797579 | |||||
| chr3:15797646
|
G | C | 1 | a0001c0001t0056 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1125C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1125 | chr3 | 15797646 | |||||
| chr3:15797657
|
G | A | 1 | a0001c0005t0057 | 1 | HG03225.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1136C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797657 | ||||||
| chr3:15797717
|
C | T | 1 | a0001c0001t0023 | 1 | NA18969.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1196G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1196 | chr3 | 15797717 | |||||
| chr3:15797728
|
T | C | 5 | a0001c0001t0008a0001c0001t0015a0001c0001t0016others(2): Show | 16 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(13): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1207A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | chr3 | 15797728 | ||||||
| chr3:15797924
|
A | C | 1 | a0001c0002t0022 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1403T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/28 | 1403 | chr3 | 15797924 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15670582
|
A | T | 1 | a0001c0002t0001g0138 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2966-26T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670582 | ||||||
| chr3:15670592
|
C | T | 1 | a0001c0001t0044g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2966-36G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670592 | ||||||
| chr3:15670629
|
A | C | 1 | a0001c0004t0009g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2966-73T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670629 | ||||||
| chr3:15670696
|
T | A | 1 | a0001c0001t0002g0048 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2966-140A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670696 | ||||||
| chr3:15670815
|
A | G | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2966-259T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670815 | ||||||
| chr3:15670862
|
A | G | 7 | a0001c0001t0008g0331a0001c0001t0008g0332a0001c0001t0008g0335others(4): Show | 7 | HG02896.hp2 HG03130.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2966-306T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15670862 | ||||||
| chr3:15671042
|
C | T | 2 | a0001c0002t0001g0204a0001c0002t0001g0205 | 2 | HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.2966-486G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671042 | ||||||
| chr3:15671322
|
C | T | 1 | a0001c0001t0008g0337 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2966-766G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671322 | ||||||
| chr3:15671353
|
G | T | 1 | a0001c0001t0002g0024 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2966-797C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671353 | ||||||
| chr3:15671364
|
A | G | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2966-808T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671364 | ||||||
| chr3:15671576
|
T | C | 39 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(36): Show | 40 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.2966-1020A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671576 | ||||||
| chr3:15671578
|
G | GT | 17 | a0001c0002t0001g0214a0001c0002t0001g0225a0001c0002t0040g0108others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.2966-1023dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671578 | ||||||
| chr3:15671578
|
G | T | 1 | a0001c0003t0005g0286 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2966-1022C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671578 | ||||||
| chr3:15671589
|
G | T | 24 | a0001c0001t0002g0085a0001c0003t0005g0281a0001c0003t0005g0282others(21): Show | 24 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.2966-1033C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671589 | ||||||
| chr3:15671618
|
C | T | 1 | a0001c0002t0048g0226 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2966-1062G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671618 | ||||||
| chr3:15671668
|
T | C | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2966-1112A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671668 | ||||||
| chr3:15671836
|
C | T | 10 | a0001c0001t0002g0076a0001c0004t0009g0294a0001c0004t0009g0295others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2966-1280G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671836 | ||||||
| chr3:15671953
|
A | G | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2966-1397T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15671953 | ||||||
| chr3:15672062
|
T | C | 1 | a0001c0002t0001g0128 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2966-1506A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672062 | ||||||
| chr3:15672146
|
A | AT | 18 | a0001c0001t0002g0054a0001c0001t0002g0085a0001c0001t0004g0238others(15): Show | 18 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2966-1591dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672146 | ||||||
| chr3:15672146
|
AT | A | 27 | a0001c0001t0003g0256a0001c0003t0005g0281a0001c0003t0005g0282others(24): Show | 27 | HG01109.hp2 HG01168.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2966-1591delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672146 | ||||||
| chr3:15672146
|
ATT | A | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2966-1592_2966-159 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672146 | ||||||
| chr3:15672172
|
G | T | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2966-1616C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672172 | ||||||
| chr3:15672215
|
G | A | 1 | a0001c0003t0005g0287 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2966-1659C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672215 | ||||||
| chr3:15672419
|
G | A | 8 | a0001c0004t0009g0295a0001c0004t0009g0296a0001c0004t0009g0297others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2966-1863C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672419 | ||||||
| chr3:15672437
|
C | A | 1 | a0001c0002t0001g0144 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2966-1881G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672437 | ||||||
| chr3:15672844
|
C | T | 2 | a0001c0001t0008g0331a0001c0001t0008g0332 | 2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2966-2288G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672844 | ||||||
| chr3:15672984
|
G | A | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2966-2428C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15672984 | ||||||
| chr3:15673028
|
GT | G | 338 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.2966-2473delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673028 | ||||||
| chr3:15673192
|
T | C | 1 | a0001c0001t0004g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2966-2636A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673192 | ||||||
| chr3:15673381
|
G | A | 1 | a0001c0001t0003g0257 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2965+2517C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673381 | ||||||
| chr3:15673438
|
T | A | 1 | a0001c0001t0002g0054 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2965+2460A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673438 | ||||||
| chr3:15673480
|
C | T | 20 | a0001c0002t0001g0183a0001c0002t0001g0194a0001c0002t0001g0195others(17): Show | 20 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.2965+2418G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673480 | ||||||
| chr3:15673642
|
A | G | 5 | a0001c0002t0017g0227a0001c0002t0017g0228a0001c0007t0021g0302others(2): Show | 5 | HG00597.hp1 NA18956.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.2965+2256T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673642 | ||||||
| chr3:15673649
|
G | C | 129 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2965+2249C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673649 | ||||||
| chr3:15673650
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2965+2248T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673650 | ||||||
| chr3:15673856
|
A | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | HG02155.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2965+2042T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673856 | ||||||
| chr3:15673979
|
C | T | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2965+1919G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15673979 | ||||||
| chr3:15674050
|
T | C | 1 | a0001c0002t0001g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2965+1848A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674050 | ||||||
| chr3:15674154
|
A | C | 1 | a0001c0001t0004g0245 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2965+1744T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674154 | ||||||
| chr3:15674174
|
C | CA | 16 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0245others(13): Show | 16 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.2965+1723dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | ||||||
| chr3:15674174
|
C | CAAA | 13 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0286others(10): Show | 13 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2965+1721_2965+172 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | ||||||
| chr3:15674174
|
C | CAAAAA | 25 | a0001c0001t0006g0309a0001c0002t0001g0136a0001c0002t0001g0137others(22): Show | 25 | HG00099.hp2 HG00642.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2965+1719_2965+172 others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | ||||||
| chr3:15674174
|
C | CAAAAAA | 75 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(72): Show | 75 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.2965+1718_2965+172 others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | ||||||
| chr3:15674174
|
C | CAAAAAAA | 25 | a0001c0001t0044g0178a0001c0002t0001g0118a0001c0002t0001g0124others(22): Show | 25 | HG00423.hp1 HG00673.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.2965+1717_2965+172 others(11): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | ||||||
| chr3:15674174
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0055g0321 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2965+1713_2965+172 others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | ||||||
| chr3:15674174
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2965+1714_2965+172 others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674174 | ||||||
| chr3:15674196
|
A | AAAAAAAA others(24): Show |
1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2965+1701_2965+170 others(35): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | ||||||
| chr3:15674196
|
A | AAAAAAAA others(4): Show |
2 | a0001c0001t0002g0045a0001c0001t0002g0055 | 2 | NA18986.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2965+1701_2965+170 others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | ||||||
| chr3:15674196
|
A | AAAAAAAA others(3): Show |
1 | a0004c0008t0002g0088 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2965+1701_2965+170 others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | ||||||
| chr3:15674196
|
A | AAAAAAAA others(2): Show |
10 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0022others(7): Show | 10 | HG00423.hp2 HG02132.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.2965+1701_2965+170 others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | ||||||
| chr3:15674196
|
A | AAAAAAAA others(1): Show |
34 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(31): Show | 34 | HG00597.hp2 HG01099.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.2965+1701_2965+170 others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | ||||||
| chr3:15674196
|
A | AAAAAAAG | 64 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0033others(61): Show | 65 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.2965+1701_2965+170 others(11): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | ||||||
| chr3:15674196
|
A | G | 3 | a0001c0001t0002g0076a0001c0001t0002g0085a0001c0001t0002g0087 | 3 | NA19001.hp2 NA19011.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2965+1702T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674196 | ||||||
| chr3:15674199
|
G | T | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2965+1699C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674199 | ||||||
| chr3:15674400
|
GT | G | 313 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(310): Show | 314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.2965+1497delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674400 | ||||||
| chr3:15674498
|
A | G | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2965+1400T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674498 | ||||||
| chr3:15674543
|
C | A | 1 | a0001c0001t0002g0021 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2965+1355G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674543 | ||||||
| chr3:15674718
|
G | C | 1 | a0001c0002t0001g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2965+1180C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674718 | ||||||
| chr3:15674746
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2965+1152C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674746 | ||||||
| chr3:15674761
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2965+1137A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674761 | ||||||
| chr3:15674821
|
A | C | 1 | a0002c0006t0001g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2965+1077T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674821 | ||||||
| chr3:15674896
|
T | C | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2965+1002A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674896 | ||||||
| chr3:15674955
|
C | T | 109 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(106): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2965+943G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674955 | ||||||
| chr3:15674960
|
C | A | 1 | a0001c0004t0009g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2965+938G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674960 | ||||||
| chr3:15674977
|
T | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2965+921A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15674977 | ||||||
| chr3:15675003
|
C | T | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2965+895G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675003 | ||||||
| chr3:15675185
|
C | T | 129 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2965+713G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675185 | ||||||
| chr3:15675266
|
G | A | 4 | a0002c0006t0001g0135a0002c0006t0001g0202a0002c0006t0001g0203others(1): Show | 4 | HG00642.hp1 HG01109.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2965+632C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675266 | ||||||
| chr3:15675332
|
G | T | 1 | a0001c0002t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2965+566C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675332 | ||||||
| chr3:15675391
|
C | T | 152 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2965+507G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675391 | ||||||
| chr3:15675534
|
G | A | 1 | a0001c0005t0012g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2965+364C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675534 | ||||||
| chr3:15675617
|
G | C | 127 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.2965+281C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675617 | ||||||
| chr3:15675692
|
C | T | 1 | a0001c0001t0004g0249 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2965+206G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 27/27 | chr3 | 15675692 | ||||||
| chr3:15676107
|
G | A | 10 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0138others(7): Show | 10 | HG00642.hp2 HG01071.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2874-118C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676107 | ||||||
| chr3:15676134
|
G | A | 13 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(10): Show | 13 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.2874-145C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676134 | ||||||
| chr3:15676186
|
G | A | 125 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2874-197C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676186 | ||||||
| chr3:15676195
|
G | A | 1 | a0001c0001t0015g0326 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2874-206C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676195 | ||||||
| chr3:15676265
|
T | A | 1 | a0001c0002t0038g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2874-276A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676265 | ||||||
| chr3:15676337
|
C | T | 128 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.2874-348G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676337 | ||||||
| chr3:15676455
|
C | T | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2874-466G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676455 | ||||||
| chr3:15676637
|
C | G | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2873+337G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676637 | ||||||
| chr3:15676881
|
A | G | 1 | a0001c0002t0017g0228 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2873+93T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676881 | ||||||
| chr3:15676891
|
A | G | 1 | a0001c0001t0003g0253 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2873+83T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 26/27 | chr3 | 15676891 | ||||||
| chr3:15677145
|
T | A | 156 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(153): Show | 156 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.2791-89A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 25/27 | chr3 | 15677145 | ||||||
| chr3:15677436
|
GTTAATA | G | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2790+38_2790+43del others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 25/27 | chr3 | 15677436 | ||||||
| chr3:15677701
|
A | G | 3 | a0001c0001t0001g0166a0001c0001t0003g0264a0001c0001t0003g0265 | 3 | HG01069.hp1 HG01071.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2708-139T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677701 | ||||||
| chr3:15677760
|
A | G | 1 | a0001c0003t0005g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2708-198T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677760 | ||||||
| chr3:15677772
|
T | C | 46 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(43): Show | 46 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.2708-210A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677772 | ||||||
| chr3:15677813
|
A | C | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2708-251T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677813 | ||||||
| chr3:15677856
|
C | T | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2708-294G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677856 | ||||||
| chr3:15677869
|
C | T | 2 | a0001c0001t0003g0261a0001c0001t0003g0263 | 2 | HG01243.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2708-307G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677869 | ||||||
| chr3:15677889
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2707+320A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677889 | ||||||
| chr3:15677933
|
A | C | 1 | a0001c0003t0019g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2707+276T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677933 | ||||||
| chr3:15677964
|
A | C | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2707+245T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 24/27 | chr3 | 15677964 | ||||||
| chr3:15678421
|
T | C | 1 | a0001c0002t0040g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2562-67A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 23/27 | chr3 | 15678421 | ||||||
| chr3:15678615
|
T | G | 121 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(118): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.2562-261A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 23/27 | chr3 | 15678615 | ||||||
| chr3:15678881
|
G | A | 109 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(106): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2561+420C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 23/27 | chr3 | 15678881 | ||||||
| chr3:15679135
|
C | CT | 6 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0036g0104others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2561+165dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 23/27 | chr3 | 15679135 | ||||||
| chr3:15679447
|
C | G | 1 | a0002c0006t0001g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2477+29G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 22/27 | chr3 | 15679447 | ||||||
| chr3:15679467
|
T | G | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2477+9A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 22/27 | chr3 | 15679467 | ||||||
| chr3:15679647
|
A | G | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2390-84T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15679647 | ||||||
| chr3:15679762
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2390-199G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15679762 | ||||||
| chr3:15679900
|
A | ATTATT | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2390-338_2390-337i others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15679900 | ||||||
| chr3:15679903
|
C | CCCTAAAT others(1): Show |
16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0286others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2390-341_2390-340i others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15679903 | ||||||
| chr3:15680765
|
A | C | 2 | a0001c0003t0018g0232a0001c0003t0018g0233 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1202T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680765 | ||||||
| chr3:15680769
|
G | C | 2 | a0001c0003t0018g0232a0001c0003t0018g0233 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1206C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680769 | ||||||
| chr3:15680771
|
T | A | 2 | a0001c0003t0018g0232a0001c0003t0018g0233 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1208A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680771 | ||||||
| chr3:15680777
|
C | G | 2 | a0001c0003t0018g0232a0001c0003t0018g0233 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1214G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680777 | ||||||
| chr3:15680778
|
A | G | 2 | a0001c0003t0018g0232a0001c0003t0018g0233 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1215T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680778 | ||||||
| chr3:15680779
|
C | G | 2 | a0001c0003t0018g0232a0001c0003t0018g0233 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2390-1216G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680779 | ||||||
| chr3:15680880
|
T | C | 6 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0036g0104others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2390-1317A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15680880 | ||||||
| chr3:15681015
|
A | G | 1 | a0001c0001t0008g0336 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2390-1452T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681015 | ||||||
| chr3:15681367
|
C | G | 34 | a0001c0002t0017g0227a0001c0002t0017g0228a0001c0003t0005g0281others(31): Show | 34 | HG00597.hp1 HG01109.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.2390-1804G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681367 | ||||||
| chr3:15681378
|
G | A | 6 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0036g0104others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2390-1815C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681378 | ||||||
| chr3:15681670
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2390-2107T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681670 | ||||||
| chr3:15681679
|
T | A | 1 | a0001c0002t0030g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2390-2116A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681679 | ||||||
| chr3:15681719
|
T | C | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2390-2156A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681719 | ||||||
| chr3:15681835
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2390-2272G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681835 | ||||||
| chr3:15681955
|
C | T | 1 | a0001c0002t0001g0181 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2390-2392G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15681955 | ||||||
| chr3:15682078
|
C | T | 1 | a0001c0001t0032g0066 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2390-2515G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682078 | ||||||
| chr3:15682079
|
G | A | 16 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(13): Show | 16 | HG00597.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.2390-2516C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682079 | ||||||
| chr3:15682344
|
C | T | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2390-2781G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682344 | ||||||
| chr3:15682584
|
C | T | 1 | a0001c0001t0003g0261 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2389+2642G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682584 | ||||||
| chr3:15682619
|
C | T | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2389+2607G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682619 | ||||||
| chr3:15682626
|
T | G | 127 | a0001c0001t0044g0178a0001c0002t0001g0112a0001c0002t0001g0113others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.2389+2600A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682626 | ||||||
| chr3:15682736
|
G | A | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2389+2490C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682736 | ||||||
| chr3:15682839
|
T | C | 124 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(121): Show | 125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.2389+2387A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15682839 | ||||||
| chr3:15683023
|
T | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2389+2203A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683023 | ||||||
| chr3:15683172
|
A | G | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2389+2054T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683172 | ||||||
| chr3:15683304
|
T | C | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2389+1922A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683304 | ||||||
| chr3:15683597
|
G | A | 3 | a0001c0001t0003g0254a0001c0001t0003g0261a0001c0001t0003g0263 | 3 | HG01167.hp1 HG01243.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2389+1629C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683597 | ||||||
| chr3:15683856
|
A | G | 2 | a0001c0001t0015g0324a0001c0001t0015g0325 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2389+1370T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683856 | ||||||
| chr3:15683945
|
G | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2389+1281C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683945 | ||||||
| chr3:15683965
|
C | T | 8 | a0001c0002t0017g0227a0001c0002t0017g0228a0001c0005t0012g0318others(5): Show | 8 | HG00597.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2389+1261G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15683965 | ||||||
| chr3:15684093
|
A | C | 3 | a0001c0007t0021g0302a0001c0007t0021g0303a0001c0007t0031g0049 | 3 | NA18957.hp1 NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2389+1133T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684093 | ||||||
| chr3:15684104
|
T | C | 6 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0036g0104others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2389+1122A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684104 | ||||||
| chr3:15684210
|
G | A | 6 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0036g0104others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2389+1016C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684210 | ||||||
| chr3:15684271
|
T | G | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2389+955A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684271 | ||||||
| chr3:15684286
|
T | C | 1 | a0001c0003t0005g0292 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2389+940A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684286 | ||||||
| chr3:15684298
|
T | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2389+928A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684298 | ||||||
| chr3:15684307
|
A | G | 279 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.2389+919T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684307 | ||||||
| chr3:15684392
|
A | G | 2 | a0001c0001t0002g0089a0001c0001t0002g0090 | 2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2389+834T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684392 | ||||||
| chr3:15684486
|
G | T | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2389+740C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684486 | ||||||
| chr3:15684635
|
T | C | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2389+591A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684635 | ||||||
| chr3:15684654
|
T | C | 124 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(121): Show | 125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.2389+572A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684654 | ||||||
| chr3:15684664
|
T | C | 1 | a0001c0002t0017g0228 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2389+562A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684664 | ||||||
| chr3:15684733
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2389+493T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684733 | ||||||
| chr3:15684805
|
C | G | 2 | a0001c0002t0001g0195a0001c0002t0001g0198 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2389+421G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684805 | ||||||
| chr3:15684858
|
T | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2389+368A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684858 | ||||||
| chr3:15684983
|
G | C | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2389+243C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15684983 | ||||||
| chr3:15685138
|
T | G | 1 | a0001c0004t0009g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2389+88A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15685138 | ||||||
| chr3:15685185
|
T | C | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2389+41A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 21/27 | chr3 | 15685185 | ||||||
| chr3:15685501
|
A | G | 121 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(118): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.2170-56T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 20/27 | chr3 | 15685501 | ||||||
| chr3:15685727
|
A | G | 130 | a0001c0001t0044g0178a0001c0002t0001g0112a0001c0002t0001g0113others(127): Show | 130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.2169+275T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 20/27 | chr3 | 15685727 | ||||||
| chr3:15686131
|
C | G | 6 | a0001c0002t0001g0115a0001c0002t0001g0132a0001c0002t0001g0172others(3): Show | 6 | NA18747.hp2 NA18965.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2052-12G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 19/27 | chr3 | 15686131 | ||||||
| chr3:15686183
|
C | T | 2 | a0001c0001t0015g0324a0001c0001t0015g0325 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2051+39G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 19/27 | chr3 | 15686183 | ||||||
| chr3:15686195
|
A | G | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2051+27T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 19/27 | chr3 | 15686195 | ||||||
| chr3:15686196
|
T | G | 1 | a0001c0004t0009g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2051+26A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 19/27 | chr3 | 15686196 | ||||||
| chr3:15686316
|
A | G | 112 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(109): Show | 113 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
splice_region_variant&intron_variant | LOW | c.1964-7T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686316 | ||||||
| chr3:15686449
|
A | C | 23 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(20): Show | 23 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1964-140T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686449 | ||||||
| chr3:15686740
|
C | T | 1 | a0001c0004t0009g0298 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1964-431G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686740 | ||||||
| chr3:15686845
|
C | T | 1 | a0001c0002t0041g0169 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1964-536G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686845 | ||||||
| chr3:15686901
|
C | T | 3 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0150 | 3 | HG00621.hp2 NA18945.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1964-592G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686901 | ||||||
| chr3:15686902
|
G | A | 2 | a0001c0001t0002g0073a0001c0001t0002g0074 | 2 | HG00408.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1964-593C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686902 | ||||||
| chr3:15686912
|
C | T | 6 | a0001c0001t0004g0240a0001c0001t0004g0241a0001c0001t0004g0242others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1964-603G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686912 | ||||||
| chr3:15686946
|
C | CT | 46 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(43): Show | 46 | HG00140.hp1 HG01109.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.1964-638dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686946 | ||||||
| chr3:15686947
|
T | C | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1964-638A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686947 | ||||||
| chr3:15686982
|
C | T | 16 | a0001c0002t0001g0180a0001c0002t0001g0181a0001c0002t0001g0188others(13): Show | 16 | HG00639.hp2 HG02004.hp1 HG02273.hp2 others(13): Show |
intron_variant | MODIFIER | c.1964-673G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15686982 | ||||||
| chr3:15687099
|
C | T | 3 | a0001c0003t0019g0230a0001c0003t0019g0231a0001c0003t0053g0313 | 3 | HG03209.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1964-790G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687099 | ||||||
| chr3:15687104
|
G | A | 2 | a0001c0001t0008g0331a0001c0001t0008g0332 | 2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1964-795C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687104 | ||||||
| chr3:15687106
|
C | A | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1964-797G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687106 | ||||||
| chr3:15687180
|
T | C | 276 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(273): Show | 277 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.1964-871A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687180 | ||||||
| chr3:15687223
|
A | G | 1 | a0001c0001t0002g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1964-914T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687223 | ||||||
| chr3:15687250
|
C | G | 295 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(292): Show | 296 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.1964-941G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687250 | ||||||
| chr3:15687308
|
T | C | 7 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0127others(4): Show | 7 | NA18940.hp2 NA18942.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1964-999A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687308 | ||||||
| chr3:15687332
|
G | GAT | 7 | a0001c0002t0017g0227a0001c0002t0017g0228a0001c0005t0012g0319others(4): Show | 7 | HG00597.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1964-1025_1964-102 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687332 | ||||||
| chr3:15687333
|
A | T | 1 | a0001c0001t0008g0335 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1964-1024T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687333 | ||||||
| chr3:15687547
|
A | C | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1964-1238T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687547 | ||||||
| chr3:15687566
|
G | A | 1 | a0001c0002t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1964-1257C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687566 | ||||||
| chr3:15687652
|
T | TGGAACAT others(17): Show |
1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1964-1344_1964-134 others(28): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687652 | ||||||
| chr3:15687656
|
A | G | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1964-1347T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687656 | ||||||
| chr3:15687659
|
A | T | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1964-1350T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687659 | ||||||
| chr3:15687684
|
G | T | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1964-1375C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687684 | ||||||
| chr3:15687817
|
T | G | 11 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1964-1508A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687817 | ||||||
| chr3:15687890
|
A | G | 1 | a0001c0001t0002g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1964-1581T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15687890 | ||||||
| chr3:15688062
|
T | C | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1964-1753A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688062 | ||||||
| chr3:15688078
|
T | C | 1 | a0001c0004t0009g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1964-1769A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688078 | ||||||
| chr3:15688207
|
C | G | 129 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1963+1812G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688207 | ||||||
| chr3:15688246
|
A | T | 7 | a0001c0002t0011g0236a0001c0002t0011g0237a0002c0006t0001g0135others(4): Show | 7 | HG00642.hp1 HG01109.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1963+1773T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688246 | ||||||
| chr3:15688274
|
T | C | 1 | a0001c0001t0002g0025 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1963+1745A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688274 | ||||||
| chr3:15688750
|
G | A | 129 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1963+1269C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688750 | ||||||
| chr3:15688785
|
T | C | 141 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(138): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1963+1234A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688785 | ||||||
| chr3:15688821
|
A | G | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1963+1198T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688821 | ||||||
| chr3:15688829
|
A | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1963+1190T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688829 | ||||||
| chr3:15688914
|
C | T | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1963+1105G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15688914 | ||||||
| chr3:15689372
|
T | C | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1963+647A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15689372 | ||||||
| chr3:15689528
|
G | A | 1 | a0001c0002t0001g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1963+491C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15689528 | ||||||
| chr3:15689577
|
A | G | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1963+442T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15689577 | ||||||
| chr3:15689759
|
G | C | 1 | a0001c0001t0003g0272 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1963+260C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 18/27 | chr3 | 15689759 | ||||||
| chr3:15690573
|
G | T | 1 | a0001c0003t0005g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1762-353C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690573 | ||||||
| chr3:15690653
|
C | T | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1762-433G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690653 | ||||||
| chr3:15690665
|
A | C | 2 | a0001c0001t0006g0311a0001c0001t0006g0312 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1762-445T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690665 | ||||||
| chr3:15690714
|
G | A | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1762-494C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690714 | ||||||
| chr3:15690749
|
G | T | 127 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1762-529C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690749 | ||||||
| chr3:15690778
|
G | C | 1 | a0001c0002t0001g0144 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1762-558C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690778 | ||||||
| chr3:15690786
|
C | T | 1 | a0001c0001t0003g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1762-566G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690786 | ||||||
| chr3:15690895
|
A | G | 1 | a0001c0002t0001g0148 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1762-675T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690895 | ||||||
| chr3:15690896
|
G | T | 1 | a0001c0002t0001g0148 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1762-676C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15690896 | ||||||
| chr3:15691032
|
T | G | 135 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1762-812A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691032 | ||||||
| chr3:15691037
|
A | T | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1762-817T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691037 | ||||||
| chr3:15691125
|
CT | C | 11 | a0001c0001t0002g0033a0001c0001t0002g0093a0001c0001t0004g0247others(8): Show | 11 | HG00558.hp2 HG01169.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.1762-906delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691125 | ||||||
| chr3:15691218
|
G | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1762-998C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691218 | ||||||
| chr3:15691280
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1762-1060A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691280 | ||||||
| chr3:15691366
|
G | A | 153 | a0001c0001t0002g0084a0001c0002t0001g0112a0001c0002t0001g0113others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1762-1146C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691366 | ||||||
| chr3:15691489
|
T | C | 1 | a0001c0004t0009g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1762-1269A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691489 | ||||||
| chr3:15691654
|
T | C | 5 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0127others(2): Show | 5 | NA18942.hp2 NA18966.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-1434A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691654 | ||||||
| chr3:15691707
|
T | C | 38 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(35): Show | 39 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.1762-1487A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691707 | ||||||
| chr3:15691838
|
G | T | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1762-1618C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691838 | ||||||
| chr3:15691998
|
G | A | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1762-1778C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15691998 | ||||||
| chr3:15692005
|
TG | T | 7 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0091others(4): Show | 7 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1762-1786delC | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692005 | ||||||
| chr3:15692011
|
ATGCCT | A | 7 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0091others(4): Show | 7 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1762-1796_1762-179 others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692011 | ||||||
| chr3:15692017
|
G | C | 7 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0091others(4): Show | 7 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1762-1797C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692017 | ||||||
| chr3:15692045
|
C | T | 137 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1762-1825G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692045 | ||||||
| chr3:15692063
|
C | G | 1 | a0001c0001t0002g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1762-1843G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692063 | ||||||
| chr3:15692093
|
A | T | 154 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1762-1873T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692093 | ||||||
| chr3:15692139
|
C | T | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1762-1919G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692139 | ||||||
| chr3:15692144
|
T | TA | 123 | a0001c0001t0002g0023a0001c0001t0002g0039a0001c0001t0015g0325others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1762-1925dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692144 | ||||||
| chr3:15692144
|
T | TAA | 40 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(37): Show | 41 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1762-1926_1762-192 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692144 | ||||||
| chr3:15692147
|
A | T | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1762-1927T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692147 | ||||||
| chr3:15692285
|
C | A | 26 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0118others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1762-2065G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692285 | ||||||
| chr3:15692337
|
T | C | 1 | a0001c0001t0002g0074 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1762-2117A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692337 | ||||||
| chr3:15692390
|
T | C | 166 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1762-2170A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692390 | ||||||
| chr3:15692589
|
C | G | 156 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(153): Show | 156 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1761+2150G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692589 | ||||||
| chr3:15692813
|
T | C | 3 | a0001c0001t0004g0242a0001c0001t0004g0244a0001c0001t0004g0249 | 3 | HG02258.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1761+1926A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692813 | ||||||
| chr3:15692814
|
A | G | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1761+1925T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692814 | ||||||
| chr3:15692863
|
G | T | 1 | a0001c0001t0003g0261 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1761+1876C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692863 | ||||||
| chr3:15692946
|
G | A | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+1793C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692946 | ||||||
| chr3:15692948
|
C | A | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1761+1791G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15692948 | ||||||
| chr3:15693146
|
C | A | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1761+1593G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693146 | ||||||
| chr3:15693194
|
A | T | 2 | a0001c0002t0001g0134a0001c0002t0042g0133 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1761+1545T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693194 | ||||||
| chr3:15693206
|
C | T | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1761+1533G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693206 | ||||||
| chr3:15693246
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1761+1493A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693246 | ||||||
| chr3:15693327
|
C | CAG | 13 | a0001c0002t0030g0010a0001c0003t0005g0281a0001c0003t0005g0282others(10): Show | 13 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1761+1410_1761+141 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693327 | ||||||
| chr3:15693376
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1761+1363G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693376 | ||||||
| chr3:15693405
|
A | C | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1761+1334T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693405 | ||||||
| chr3:15693426
|
G | A | 2 | a0001c0001t0008g0331a0001c0001t0008g0332 | 2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1761+1313C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693426 | ||||||
| chr3:15693428
|
GT | G | 338 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1761+1310delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693428 | ||||||
| chr3:15693474
|
A | G | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1761+1265T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693474 | ||||||
| chr3:15693517
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1761+1222A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693517 | ||||||
| chr3:15693544
|
C | G | 163 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1761+1195G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693544 | ||||||
| chr3:15693605
|
A | ATGC | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1761+1131_1761+113 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693605 | ||||||
| chr3:15693930
|
G | A | 1 | a0001c0001t0008g0335 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1761+809C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15693930 | ||||||
| chr3:15694115
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1761+624A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694115 | ||||||
| chr3:15694146
|
T | A | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1761+593A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694146 | ||||||
| chr3:15694214
|
G | GA | 131 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1761+524dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694214 | ||||||
| chr3:15694360
|
C | T | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1761+379G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694360 | ||||||
| chr3:15694493
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1761+246C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694493 | ||||||
| chr3:15694612
|
T | G | 1 | a0001c0002t0001g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1761+127A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694612 | ||||||
| chr3:15694717
|
C | T | 1 | a0001c0002t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1761+22G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694717 | ||||||
| chr3:15694723
|
T | A | 1 | a0001c0001t0002g0032 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1761+16A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 17/27 | chr3 | 15694723 | ||||||
| chr3:15694838
|
T | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01433.hp2 NA18940.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1687-25A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 16/27 | chr3 | 15694838 | ||||||
| chr3:15694878
|
A | T | 338 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1687-65T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 16/27 | chr3 | 15694878 | ||||||
| chr3:15695164
|
G | A | 2 | a0001c0001t0002g0035a0001c0005t0012g0318 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1686+24C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 16/27 | chr3 | 15695164 | ||||||
| chr3:15695304
|
C | T | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1660-90G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695304 | ||||||
| chr3:15695321
|
C | T | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1660-107G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695321 | ||||||
| chr3:15695424
|
C | T | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1660-210G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695424 | ||||||
| chr3:15695436
|
G | C | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1660-222C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695436 | ||||||
| chr3:15695510
|
G | A | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1660-296C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695510 | ||||||
| chr3:15695539
|
C | G | 1 | a0001c0002t0001g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1660-325G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695539 | ||||||
| chr3:15695549
|
T | C | 2 | a0001c0002t0001g0199a0001c0005t0012g0319 | 2 | HG00099.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1660-335A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695549 | ||||||
| chr3:15695652
|
G | A | 1 | a0001c0002t0001g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1660-438C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695652 | ||||||
| chr3:15695742
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1659+392A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695742 | ||||||
| chr3:15695771
|
C | T | 1 | a0001c0005t0057g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1659+363G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695771 | ||||||
| chr3:15695807
|
C | T | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02615.hp2 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1659+327G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15695807 | ||||||
| chr3:15696103
|
T | C | 140 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1659+31A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 15/27 | chr3 | 15696103 | ||||||
| chr3:15696317
|
A | G | 1 | a0001c0001t0033g0101 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1548-72T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696317 | ||||||
| chr3:15696375
|
C | T | 3 | a0001c0005t0012g0318a0001c0010t0012g0316a0001c0010t0012g0317 | 3 | HG02622.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1548-130G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696375 | ||||||
| chr3:15696463
|
G | A | 1 | a0001c0002t0001g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1548-218C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696463 | ||||||
| chr3:15696583
|
C | T | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1548-338G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696583 | ||||||
| chr3:15696620
|
T | C | 1 | a0002c0006t0001g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1548-375A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696620 | ||||||
| chr3:15696675
|
A | T | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1548-430T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696675 | ||||||
| chr3:15696808
|
G | A | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1548-563C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696808 | ||||||
| chr3:15696833
|
A | C | 6 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0127others(3): Show | 6 | NA18942.hp2 NA18951.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1548-588T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696833 | ||||||
| chr3:15696882
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1548-637A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696882 | ||||||
| chr3:15696952
|
A | G | 1 | a0001c0002t0040g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1548-707T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15696952 | ||||||
| chr3:15697011
|
G | A | 16 | a0001c0001t0002g0055a0001c0001t0002g0057a0001c0001t0002g0058others(13): Show | 16 | HG00597.hp2 HG00673.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.1548-766C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697011 | ||||||
| chr3:15697066
|
C | G | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-821G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697066 | ||||||
| chr3:15697139
|
G | A | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1548-894C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697139 | ||||||
| chr3:15697214
|
G | A | 1 | a0001c0003t0019g0230 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1548-969C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697214 | ||||||
| chr3:15697282
|
G | C | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1548-1037C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697282 | ||||||
| chr3:15697363
|
T | C | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1548-1118A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697363 | ||||||
| chr3:15697477
|
A | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1548-1232T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697477 | ||||||
| chr3:15697504
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1548-1259C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697504 | ||||||
| chr3:15697511
|
T | G | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-1266A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697511 | ||||||
| chr3:15697612
|
T | G | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1548-1367A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697612 | ||||||
| chr3:15697674
|
C | T | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-1429G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697674 | ||||||
| chr3:15697697
|
T | C | 257 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(254): Show | 258 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1548-1452A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697697 | ||||||
| chr3:15697839
|
C | T | 1 | a0001c0005t0012g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1548-1594G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697839 | ||||||
| chr3:15697894
|
T | C | 131 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1548-1649A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15697894 | ||||||
| chr3:15698017
|
C | T | 8 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0020g0300others(5): Show | 8 | HG02145.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1548-1772G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698017 | ||||||
| chr3:15698077
|
T | C | 1 | a0001c0001t0002g0098 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1548-1832A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698077 | ||||||
| chr3:15698174
|
C | T | 4 | a0001c0002t0001g0159a0001c0002t0001g0185a0001c0002t0001g0186others(1): Show | 4 | HG00558.hp1 NA19000.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548-1929G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698174 | ||||||
| chr3:15698177
|
C | A | 2 | a0001c0003t0018g0232a0001c0003t0018g0233 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1548-1932G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698177 | ||||||
| chr3:15698270
|
C | A | 24 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0118others(21): Show | 24 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1548-2025G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698270 | ||||||
| chr3:15698299
|
A | C | 131 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1548-2054T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698299 | ||||||
| chr3:15698314
|
C | T | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1548-2069G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698314 | ||||||
| chr3:15698329
|
C | T | 1 | a0001c0001t0004g0240 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1548-2084G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698329 | ||||||
| chr3:15698336
|
G | A | 279 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1548-2091C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698336 | ||||||
| chr3:15698368
|
T | C | 251 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(248): Show | 252 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.1548-2123A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698368 | ||||||
| chr3:15698566
|
G | A | 24 | a0001c0002t0001g0119a0001c0002t0001g0120a0001c0002t0001g0121others(21): Show | 24 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1548-2321C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698566 | ||||||
| chr3:15698578
|
G | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1548-2333C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698578 | ||||||
| chr3:15698675
|
A | C | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1548-2430T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698675 | ||||||
| chr3:15698872
|
C | G | 120 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(117): Show | 121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1548-2627G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698872 | ||||||
| chr3:15698935
|
C | G | 1 | a0001c0002t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1548-2690G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698935 | ||||||
| chr3:15698951
|
G | T | 135 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1548-2706C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15698951 | ||||||
| chr3:15699122
|
C | T | 1 | a0001c0002t0001g0199 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1548-2877G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699122 | ||||||
| chr3:15699211
|
C | G | 1 | a0001c0001t0002g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1548-2966G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699211 | ||||||
| chr3:15699287
|
C | T | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548-3042G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699287 | ||||||
| chr3:15699392
|
G | A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-3147C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699392 | ||||||
| chr3:15699396
|
TCTAATTA others(3): Show |
T | 1 | a0001c0002t0001g0157 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1548-3161_1548-315 others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699396 | ||||||
| chr3:15699502
|
G | A | 131 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1548-3257C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699502 | ||||||
| chr3:15699624
|
A | G | 1 | a0001c0001t0008g0337 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1548-3379T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699624 | ||||||
| chr3:15699755
|
G | A | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02615.hp2 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1548-3510C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699755 | ||||||
| chr3:15699789
|
A | C | 1 | a0001c0005t0057g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1548-3544T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699789 | ||||||
| chr3:15699882
|
T | C | 131 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1548-3637A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699882 | ||||||
| chr3:15699932
|
A | C | 268 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(265): Show | 269 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1548-3687T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699932 | ||||||
| chr3:15699936
|
G | A | 14 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(11): Show | 14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1548-3691C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15699936 | ||||||
| chr3:15700092
|
A | G | 279 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1548-3847T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700092 | ||||||
| chr3:15700169
|
C | T | 24 | a0001c0002t0001g0119a0001c0002t0001g0120a0001c0002t0001g0121others(21): Show | 24 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1548-3924G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700169 | ||||||
| chr3:15700286
|
G | A | 156 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(153): Show | 156 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1548-4041C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700286 | ||||||
| chr3:15700300
|
G | T | 1 | a0001c0001t0008g0331 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1548-4055C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700300 | ||||||
| chr3:15700304
|
G | A | 7 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0002g0044others(4): Show | 7 | HG00423.hp2 HG02132.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.1548-4059C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700304 | ||||||
| chr3:15700306
|
G | GC | 5 | a0001c0001t0002g0038a0001c0001t0015g0325a0001c0002t0001g0148others(2): Show | 5 | HG02056.hp2 HG03927.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548-4062dupG | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700306 | ||||||
| chr3:15700458
|
C | CA | 154 | a0001c0001t0002g0038a0001c0001t0002g0070a0001c0002t0001g0112others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1548-4214dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700458 | ||||||
| chr3:15700502
|
G | A | 1 | a0001c0005t0057g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1548-4257C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700502 | ||||||
| chr3:15700502
|
G | C | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1548-4257C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700502 | ||||||
| chr3:15700542
|
G | A | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1548-4297C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700542 | ||||||
| chr3:15700599
|
T | A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-4354A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700599 | ||||||
| chr3:15700599
|
T | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1548-4354A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700599 | ||||||
| chr3:15700632
|
G | C | 1 | a0001c0001t0002g0095 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1548-4387C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700632 | ||||||
| chr3:15700646
|
C | T | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1548-4401G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700646 | ||||||
| chr3:15700730
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG00423.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1548-4485G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700730 | ||||||
| chr3:15700731
|
G | A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-4486C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700731 | ||||||
| chr3:15700782
|
A | G | 46 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(43): Show | 46 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1548-4537T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700782 | ||||||
| chr3:15700829
|
A | G | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-4584T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700829 | ||||||
| chr3:15700830
|
A | G | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548-4585T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15700830 | ||||||
| chr3:15701002
|
C | T | 1 | a0001c0002t0001g0145 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1548-4757G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701002 | ||||||
| chr3:15701158
|
T | C | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1548-4913A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701158 | ||||||
| chr3:15701315
|
T | C | 320 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(317): Show | 321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1548-5070A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701315 | ||||||
| chr3:15701401
|
T | C | 1 | a0001c0002t0001g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1548-5156A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701401 | ||||||
| chr3:15701528
|
C | T | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1548-5283G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701528 | ||||||
| chr3:15701569
|
A | T | 7 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(4): Show | 7 | HG01433.hp2 NA18940.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548-5324T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701569 | ||||||
| chr3:15701622
|
CAAG | C | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-5380_1548-537 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701622 | ||||||
| chr3:15701647
|
A | AAAAT | 7 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0020g0300others(4): Show | 7 | HG02145.hp2 HG02622.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1548-5406_1548-540 others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701647 | ||||||
| chr3:15701647
|
A | AAAATAAA others(9): Show |
1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1548-5418_1548-540 others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701647 | ||||||
| chr3:15701696
|
T | C | 10 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0138others(7): Show | 10 | HG00642.hp2 HG01071.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1548-5451A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701696 | ||||||
| chr3:15701947
|
A | G | 1 | a0001c0001t0023g0003 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1548-5702T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701947 | ||||||
| chr3:15701972
|
T | TTA | 14 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(11): Show | 14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1548-5729_1548-572 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15701972 | ||||||
| chr3:15702139
|
C | T | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1547+5785G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702139 | ||||||
| chr3:15702214
|
C | T | 179 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(176): Show | 179 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1547+5710G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702214 | ||||||
| chr3:15702245
|
C | G | 8 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0020g0300others(5): Show | 8 | HG02145.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1547+5679G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702245 | ||||||
| chr3:15702337
|
A | G | 177 | a0001c0001t0003g0260a0001c0001t0006g0304a0001c0001t0006g0305others(174): Show | 177 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.1547+5587T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702337 | ||||||
| chr3:15702357
|
G | A | 2 | a0001c0002t0001g0163a0001c0002t0001g0164 | 2 | NA18969.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1547+5567C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702357 | ||||||
| chr3:15702383
|
C | T | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1547+5541G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702383 | ||||||
| chr3:15702419
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1547+5505C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702419 | ||||||
| chr3:15702443
|
C | G | 3 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0011g0235 | 3 | NA18948.hp2 NA18967.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1547+5481G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702443 | ||||||
| chr3:15702659
|
T | C | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547+5265A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702659 | ||||||
| chr3:15702689
|
G | C | 1 | a0001c0002t0001g0148 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1547+5235C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702689 | ||||||
| chr3:15702899
|
A | G | 120 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(117): Show | 121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1547+5025T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15702899 | ||||||
| chr3:15703303
|
A | C | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1547+4621T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703303 | ||||||
| chr3:15703422
|
A | G | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547+4502T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703422 | ||||||
| chr3:15703595
|
C | G | 1 | a0001c0001t0039g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1547+4329G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703595 | ||||||
| chr3:15703653
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1547+4271G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703653 | ||||||
| chr3:15703746
|
G | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1547+4178C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703746 | ||||||
| chr3:15703915
|
A | G | 1 | a0001c0005t0057g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1547+4009T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15703915 | ||||||
| chr3:15704041
|
T | C | 1 | a0001c0001t0006g0306 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1547+3883A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704041 | ||||||
| chr3:15704197
|
T | C | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | HG02155.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1547+3727A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704197 | ||||||
| chr3:15704204
|
A | G | 1 | a0001c0001t0002g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1547+3720T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704204 | ||||||
| chr3:15704299
|
T | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | NA18986.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1547+3625A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704299 | ||||||
| chr3:15704703
|
AT | A | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547+3220delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704703 | ||||||
| chr3:15704727
|
T | C | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1547+3197A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704727 | ||||||
| chr3:15704767
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1547+3157T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704767 | ||||||
| chr3:15704830
|
C | A | 1 | a0001c0001t0003g0262 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1547+3094G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704830 | ||||||
| chr3:15704878
|
C | A | 1 | a0001c0002t0001g0167 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1547+3046G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704878 | ||||||
| chr3:15704927
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1547+2997A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15704927 | ||||||
| chr3:15705089
|
C | A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1547+2835G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705089 | ||||||
| chr3:15705236
|
A | C | 1 | a0001c0001t0002g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1547+2688T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705236 | ||||||
| chr3:15705318
|
C | T | 11 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1547+2606G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705318 | ||||||
| chr3:15705336
|
G | C | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547+2588C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705336 | ||||||
| chr3:15705353
|
G | A | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1547+2571C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705353 | ||||||
| chr3:15705430
|
G | A | 148 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.1547+2494C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705430 | ||||||
| chr3:15705453
|
T | C | 1 | a0001c0001t0002g0086 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1547+2471A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705453 | ||||||
| chr3:15705696
|
A | G | 1 | a0001c0005t0012g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1547+2228T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705696 | ||||||
| chr3:15705858
|
G | GCAC | 122 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(119): Show | 123 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1547+2065_1547+206 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15705858 | ||||||
| chr3:15706006
|
G | A | 338 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1547+1918C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706006 | ||||||
| chr3:15706047
|
C | CA | 179 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(176): Show | 179 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1547+1876dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706047 | ||||||
| chr3:15706047
|
CAAAA | C | 3 | a0001c0001t0010g0276a0001c0001t0010g0277a0001c0001t0010g0278 | 3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1547+1873_1547+187 others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706047 | ||||||
| chr3:15706071
|
T | G | 1 | a0001c0001t0059g0333 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1547+1853A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706071 | ||||||
| chr3:15706073
|
G | T | 38 | a0001c0001t0002g0011a0001c0001t0002g0033a0001c0001t0002g0034others(35): Show | 38 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1547+1851C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706073 | ||||||
| chr3:15706102
|
T | G | 3 | a0001c0001t0015g0324a0001c0001t0015g0325a0001c0001t0015g0326 | 3 | HG02683.hp2 HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1547+1822A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706102 | ||||||
| chr3:15706197
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1547+1727G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706197 | ||||||
| chr3:15706236
|
C | A | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547+1688G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706236 | ||||||
| chr3:15706359
|
C | A | 1 | a0001c0002t0001g0191 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1547+1565G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706359 | ||||||
| chr3:15706359
|
C | T | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547+1565G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706359 | ||||||
| chr3:15706379
|
T | TG | 338 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1547+1544dupC | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706379 | ||||||
| chr3:15706410
|
G | A | 2 | a0001c0002t0001g0204a0001c0002t0001g0205 | 2 | HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1547+1514C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706410 | ||||||
| chr3:15706417
|
ACTC | A | 153 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1547+1504_1547+150 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706417 | ||||||
| chr3:15706522
|
C | T | 22 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(19): Show | 22 | HG00597.hp1 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1547+1402G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706522 | ||||||
| chr3:15706533
|
A | G | 22 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(19): Show | 22 | HG00597.hp1 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1547+1391T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706533 | ||||||
| chr3:15706537
|
T | C | 1 | a0001c0002t0001g0221 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1547+1387A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706537 | ||||||
| chr3:15706539
|
A | G | 1 | a0001c0002t0001g0221 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1547+1385T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706539 | ||||||
| chr3:15706654
|
T | G | 279 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1547+1270A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706654 | ||||||
| chr3:15706723
|
C | T | 2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | NA19005.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1547+1201G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706723 | ||||||
| chr3:15706886
|
T | A | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1547+1038A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706886 | ||||||
| chr3:15706892
|
A | T | 279 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1547+1032T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706892 | ||||||
| chr3:15706945
|
A | C | 1 | a0001c0001t0003g0259 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1547+979T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15706945 | ||||||
| chr3:15707071
|
G | A | 24 | a0001c0002t0001g0119a0001c0002t0001g0120a0001c0002t0001g0121others(21): Show | 24 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1547+853C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707071 | ||||||
| chr3:15707155
|
T | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1547+769A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707155 | ||||||
| chr3:15707249
|
G | A | 4 | a0001c0001t0016g0327a0001c0001t0016g0328a0001c0001t0016g0330others(1): Show | 4 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+675C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707249 | ||||||
| chr3:15707258
|
GA | G | 137 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1547+665delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707258 | ||||||
| chr3:15707400
|
C | G | 1 | a0001c0001t0002g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1547+524G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707400 | ||||||
| chr3:15707459
|
A | G | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1547+465T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707459 | ||||||
| chr3:15707493
|
C | T | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1547+431G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707493 | ||||||
| chr3:15707706
|
C | T | 133 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(130): Show | 133 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1547+218G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707706 | ||||||
| chr3:15707807
|
A | ATT | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547+116_1547+117i others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707807 | ||||||
| chr3:15707841
|
C | A | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1547+83G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707841 | ||||||
| chr3:15707845
|
T | C | 100 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(97): Show | 101 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1547+79A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 14/27 | chr3 | 15707845 | ||||||
| chr3:15708103
|
G | A | 1 | a0001c0001t0008g0337 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1407-39C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708103 | ||||||
| chr3:15708549
|
G | A | 139 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1407-485C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708549 | ||||||
| chr3:15708573
|
T | C | 4 | a0001c0001t0016g0327a0001c0001t0016g0328a0001c0001t0016g0330others(1): Show | 4 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1407-509A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708573 | ||||||
| chr3:15708586
|
G | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1407-522C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708586 | ||||||
| chr3:15708663
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1407-599C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708663 | ||||||
| chr3:15708696
|
G | A | 126 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1407-632C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708696 | ||||||
| chr3:15708761
|
G | A | 129 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1407-697C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708761 | ||||||
| chr3:15708837
|
A | C | 259 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(256): Show | 260 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.1407-773T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708837 | ||||||
| chr3:15708985
|
C | T | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1406+683G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15708985 | ||||||
| chr3:15709182
|
G | A | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1406+486C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15709182 | ||||||
| chr3:15709377
|
T | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1406+291A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15709377 | ||||||
| chr3:15709534
|
G | C | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1406+134C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 13/27 | chr3 | 15709534 | ||||||
| chr3:15709820
|
T | A | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1338-84A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15709820 | ||||||
| chr3:15709821
|
G | A | 1 | a0001c0002t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1338-85C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15709821 | ||||||
| chr3:15709900
|
A | G | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1338-164T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15709900 | ||||||
| chr3:15710036
|
G | GT | 291 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(288): Show | 292 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.1338-301dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710036 | ||||||
| chr3:15710076
|
T | A | 150 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1338-340A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710076 | ||||||
| chr3:15710077
|
T | C | 279 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1338-341A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710077 | ||||||
| chr3:15710142
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1338-406G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710142 | ||||||
| chr3:15710398
|
G | C | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1338-662C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710398 | ||||||
| chr3:15710446
|
C | T | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1338-710G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710446 | ||||||
| chr3:15710487
|
C | G | 1 | a0001c0001t0002g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1337+724G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710487 | ||||||
| chr3:15710621
|
T | C | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1337+590A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710621 | ||||||
| chr3:15710780
|
T | C | 1 | a0001c0002t0022g0002 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1337+431A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15710780 | ||||||
| chr3:15711068
|
C | T | 1 | a0001c0002t0014g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1337+143G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15711068 | ||||||
| chr3:15711098
|
T | C | 2 | a0001c0001t0004g0238a0001c0001t0004g0239 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1337+113A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15711098 | ||||||
| chr3:15711125
|
GAATT | G | 5 | a0001c0001t0003g0256a0001c0001t0003g0257a0001c0001t0003g0258others(2): Show | 5 | NA18957.hp2 NA18961.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.1337+82_1337+85del others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 12/27 | chr3 | 15711125 | ||||||
| chr3:15711322
|
C | T | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1274-48G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711322 | ||||||
| chr3:15711323
|
T | C | 131 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1274-49A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711323 | ||||||
| chr3:15711593
|
T | C | 120 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(117): Show | 121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1274-319A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711593 | ||||||
| chr3:15711792
|
T | C | 1 | a0001c0001t0002g0056 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1273+348A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711792 | ||||||
| chr3:15711843
|
C | G | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273+297G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711843 | ||||||
| chr3:15711843
|
C | T | 131 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1273+297G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711843 | ||||||
| chr3:15711865
|
A | AT | 126 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1273+274dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711865 | ||||||
| chr3:15711865
|
A | ATT | 7 | a0001c0002t0001g0124a0001c0002t0001g0162a0001c0002t0001g0163others(4): Show | 7 | HG00673.hp1 HG02145.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1273+273_1273+274d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711865 | ||||||
| chr3:15711885
|
G | A | 1 | a0005c0011t0003g0255 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1273+255C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711885 | ||||||
| chr3:15711963
|
T | C | 6 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0036g0104others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273+177A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15711963 | ||||||
| chr3:15712002
|
C | T | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1273+138G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15712002 | ||||||
| chr3:15712029
|
T | G | 1 | a0001c0002t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1273+111A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15712029 | ||||||
| chr3:15712134
|
A | G | 126 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(123): Show |
splice_region_variant&intron_variant | LOW | c.1273+6T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 11/27 | chr3 | 15712134 | ||||||
| chr3:15712245
|
G | A | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1191-23C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712245 | ||||||
| chr3:15712361
|
A | G | 120 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(117): Show | 121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1191-139T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712361 | ||||||
| chr3:15712389
|
G | A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1191-167C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712389 | ||||||
| chr3:15712557
|
C | T | 2 | a0001c0001t0008g0334a0001c0001t0008g0339 | 2 | NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1191-335G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712557 | ||||||
| chr3:15712568
|
A | G | 1 | a0001c0001t0006g0308 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1191-346T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712568 | ||||||
| chr3:15712740
|
T | C | 259 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(256): Show | 260 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.1191-518A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15712740 | ||||||
| chr3:15713031
|
A | G | 135 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1190+496T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15713031 | ||||||
| chr3:15713342
|
C | T | 157 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1190+185G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15713342 | ||||||
| chr3:15713478
|
C | T | 20 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(17): Show | 20 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1190+49G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 10/27 | chr3 | 15713478 | ||||||
| chr3:15713669
|
C | A | 11 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1076-28G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713669 | ||||||
| chr3:15713696
|
G | A | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1076-55C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713696 | ||||||
| chr3:15713862
|
T | C | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03831.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1076-221A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713862 | ||||||
| chr3:15713889
|
A | C | 3 | a0001c0002t0001g0159a0001c0002t0001g0185a0001c0002t0001g0186 | 3 | HG00558.hp1 NA19000.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1076-248T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713889 | ||||||
| chr3:15713900
|
A | G | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1076-259T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713900 | ||||||
| chr3:15713983
|
C | T | 1 | a0001c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1076-342G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15713983 | ||||||
| chr3:15714299
|
G | A | 1 | a0001c0005t0012g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1075+279C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15714299 | ||||||
| chr3:15714532
|
G | GA | 33 | a0001c0001t0001g0166a0001c0001t0002g0017a0001c0001t0002g0035others(30): Show | 33 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1075+45dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15714532 | ||||||
| chr3:15714532
|
G | GAA | 116 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(113): Show | 116 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1075+44_1075+45dup others(2): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15714532 | ||||||
| chr3:15714532
|
G | GAAA | 10 | a0001c0002t0001g0154a0001c0002t0001g0156a0001c0002t0001g0186others(7): Show | 10 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1075+43_1075+45dup others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15714532 | ||||||
| chr3:15714552
|
A | C | 1 | a0001c0001t0006g0314 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1075+26T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 9/27 | chr3 | 15714552 | ||||||
| chr3:15714661
|
G | T | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | splice_region_variant&intron_variant | LOW | c.997-5C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15714661 | ||||||
| chr3:15714708
|
A | T | 179 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(176): Show | 179 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.997-52T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15714708 | ||||||
| chr3:15714835
|
G | A | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.997-179C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15714835 | ||||||
| chr3:15715048
|
AT | A | 3 | a0001c0001t0001g0166a0001c0001t0003g0264a0001c0001t0003g0265 | 3 | HG01069.hp1 HG01071.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.997-393delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715048 | ||||||
| chr3:15715291
|
G | A | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.997-635C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715291 | ||||||
| chr3:15715453
|
T | G | 8 | a0001c0001t0002g0011a0001c0001t0002g0033a0001c0001t0002g0034others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.997-797A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715453 | ||||||
| chr3:15715526
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.997-870A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715526 | ||||||
| chr3:15715559
|
T | C | 3 | a0001c0003t0019g0230a0001c0003t0019g0231a0001c0003t0053g0313 | 3 | HG03209.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.997-903A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715559 | ||||||
| chr3:15715766
|
G | A | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-1110C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15715766 | ||||||
| chr3:15716068
|
C | T | 1 | a0001c0001t0002g0041 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.997-1412G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716068 | ||||||
| chr3:15716069
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.997-1413C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716069 | ||||||
| chr3:15716124
|
A | C | 1 | a0001c0001t0039g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.997-1468T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716124 | ||||||
| chr3:15716281
|
C | CT | 12 | a0001c0001t0002g0015a0001c0001t0002g0045a0001c0001t0002g0094others(9): Show | 12 | HG01109.hp2 HG02602.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.997-1626dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716281 | ||||||
| chr3:15716281
|
CT | C | 20 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0093others(17): Show | 20 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.997-1626delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716281 | ||||||
| chr3:15716394
|
T | C | 132 | a0001c0001t0002g0051a0001c0002t0001g0112a0001c0002t0001g0113others(129): Show | 132 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.997-1738A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716394 | ||||||
| chr3:15716642
|
T | A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.997-1986A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716642 | ||||||
| chr3:15716674
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0002g0074 | 2 | HG00408.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.997-2018G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716674 | ||||||
| chr3:15716775
|
A | G | 1 | a0001c0002t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.997-2119T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716775 | ||||||
| chr3:15716822
|
C | T | 1 | a0001c0002t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.997-2166G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15716822 | ||||||
| chr3:15717003
|
T | G | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.997-2347A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717003 | ||||||
| chr3:15717502
|
T | G | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.997-2846A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717502 | ||||||
| chr3:15717543
|
T | G | 127 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.997-2887A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717543 | ||||||
| chr3:15717733
|
C | T | 254 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(251): Show | 255 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.997-3077G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717733 | ||||||
| chr3:15717764
|
T | A | 1 | a0001c0002t0040g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.997-3108A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717764 | ||||||
| chr3:15717853
|
T | A | 279 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.996+3062A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717853 | ||||||
| chr3:15717856
|
C | T | 1 | a0001c0001t0003g0270 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.996+3059G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717856 | ||||||
| chr3:15717899
|
T | C | 20 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(17): Show | 20 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.996+3016A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717899 | ||||||
| chr3:15717984
|
A | G | 256 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(253): Show | 257 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.996+2931T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15717984 | ||||||
| chr3:15718073
|
A | G | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.996+2842T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718073 | ||||||
| chr3:15718098
|
A | G | 1 | a0001c0002t0040g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.996+2817T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718098 | ||||||
| chr3:15718123
|
T | C | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.996+2792A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718123 | ||||||
| chr3:15718149
|
A | G | 3 | a0001c0001t0015g0324a0001c0001t0015g0325a0001c0001t0015g0326 | 3 | HG02683.hp2 HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.996+2766T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718149 | ||||||
| chr3:15718290
|
T | C | 11 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.996+2625A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718290 | ||||||
| chr3:15718442
|
T | A | 6 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0036g0104others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.996+2473A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718442 | ||||||
| chr3:15718490
|
C | T | 1 | a0001c0001t0004g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.996+2425G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718490 | ||||||
| chr3:15718550
|
T | C | 1 | a0002c0006t0001g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.996+2365A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718550 | ||||||
| chr3:15718733
|
A | C | 1 | a0001c0001t0002g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.996+2182T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718733 | ||||||
| chr3:15718789
|
A | G | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.996+2126T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718789 | ||||||
| chr3:15718833
|
C | T | 254 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(251): Show | 255 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.996+2082G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718833 | ||||||
| chr3:15718955
|
C | T | 256 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(253): Show | 257 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.996+1960G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718955 | ||||||
| chr3:15718967
|
A | G | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.996+1948T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15718967 | ||||||
| chr3:15719014
|
A | G | 3 | a0001c0002t0011g0236a0001c0002t0011g0237a0003c0015t0011g0234 | 3 | HG01255.hp1 HG01993.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.996+1901T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15719014 | ||||||
| chr3:15719252
|
C | T | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.996+1663G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15719252 | ||||||
| chr3:15719455
|
C | A | 256 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(253): Show | 257 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.996+1460G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15719455 | ||||||
| chr3:15719820
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.996+1095T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15719820 | ||||||
| chr3:15719852
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.996+1063G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15719852 | ||||||
| chr3:15720155
|
T | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.996+760A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720155 | ||||||
| chr3:15720218
|
C | CA | 20 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(17): Show | 20 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.996+696dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720218 | ||||||
| chr3:15720228
|
C | A | 1 | a0001c0004t0009g0295 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.996+687G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720228 | ||||||
| chr3:15720272
|
T | A | 1 | a0001c0001t0004g0245 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.996+643A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720272 | ||||||
| chr3:15720554
|
G | GACAAATG others(29): Show |
1 | a0002c0006t0001g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.996+325_996+360dup others(36): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720554 | ||||||
| chr3:15720613
|
C | A | 279 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.996+302G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720613 | ||||||
| chr3:15720698
|
CCCA | C | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.996+214_996+216del others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720698 | ||||||
| chr3:15720702
|
T | A | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.996+213A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 8/27 | chr3 | 15720702 | ||||||
| chr3:15721189
|
C | G | 46 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(43): Show | 46 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.784-62G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721189 | ||||||
| chr3:15721235
|
C | T | 1 | a0001c0002t0001g0139 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.784-108G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721235 | ||||||
| chr3:15721340
|
G | A | 137 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.784-213C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721340 | ||||||
| chr3:15721363
|
G | T | 3 | a0001c0001t0010g0276a0001c0001t0010g0277a0001c0001t0010g0278 | 3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.784-236C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721363 | ||||||
| chr3:15721395
|
A | G | 1 | a0001c0001t0003g0272 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.784-268T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721395 | ||||||
| chr3:15721413
|
C | T | 137 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.784-286G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721413 | ||||||
| chr3:15721588
|
A | G | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.784-461T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721588 | ||||||
| chr3:15721636
|
T | A | 5 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(2): Show | 5 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-509A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721636 | ||||||
| chr3:15721848
|
G | A | 3 | a0001c0005t0012g0318a0001c0010t0012g0316a0001c0010t0012g0317 | 3 | HG02622.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.784-721C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721848 | ||||||
| chr3:15721990
|
C | T | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.784-863G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15721990 | ||||||
| chr3:15722024
|
C | T | 7 | a0001c0001t0002g0011a0001c0001t0002g0033a0001c0001t0002g0034others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-897G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722024 | ||||||
| chr3:15722066
|
A | G | 47 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.784-939T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722066 | ||||||
| chr3:15722277
|
T | C | 1 | a0001c0001t0004g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.784-1150A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722277 | ||||||
| chr3:15722464
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.784-1337G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722464 | ||||||
| chr3:15722591
|
A | G | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.784-1464T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722591 | ||||||
| chr3:15722592
|
T | C | 1 | a0001c0001t0059g0333 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.784-1465A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722592 | ||||||
| chr3:15722921
|
C | G | 278 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(275): Show | 279 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.783+1461G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15722921 | ||||||
| chr3:15723084
|
A | AT | 11 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+1297_783+1298i others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723084 | ||||||
| chr3:15723085
|
A | C | 11 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+1297T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723085 | ||||||
| chr3:15723086
|
T | C | 11 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+1296A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723086 | ||||||
| chr3:15723119
|
C | T | 11 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+1263G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723119 | ||||||
| chr3:15723192
|
T | G | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.783+1190A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723192 | ||||||
| chr3:15723248
|
G | A | 1 | a0001c0001t0006g0305 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.783+1134C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723248 | ||||||
| chr3:15723411
|
T | C | 1 | a0001c0007t0021g0303 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.783+971A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723411 | ||||||
| chr3:15723459
|
A | T | 1 | a0001c0007t0021g0303 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.783+923T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723459 | ||||||
| chr3:15723503
|
G | A | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.783+879C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723503 | ||||||
| chr3:15723632
|
T | TA | 20 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(17): Show | 20 | HG00408.hp2 HG01433.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.783+749dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723632 | ||||||
| chr3:15723760
|
C | G | 1 | a0002c0006t0001g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.783+622G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723760 | ||||||
| chr3:15723881
|
G | A | 265 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(262): Show | 266 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.783+501C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723881 | ||||||
| chr3:15723988
|
T | C | 1 | a0001c0001t0003g0271 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.783+394A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 7/27 | chr3 | 15723988 | ||||||
| chr3:15724717
|
G | A | 1 | a0001c0002t0030g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.641-193C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15724717 | ||||||
| chr3:15724767
|
C | T | 1 | a0001c0002t0001g0199 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.641-243G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15724767 | ||||||
| chr3:15724802
|
G | A | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.641-278C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15724802 | ||||||
| chr3:15724873
|
T | G | 25 | a0001c0001t0044g0178a0001c0002t0001g0119a0001c0002t0001g0120others(22): Show | 25 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.641-349A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15724873 | ||||||
| chr3:15724981
|
G | A | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.641-457C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15724981 | ||||||
| chr3:15725186
|
T | C | 17 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(14): Show | 17 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.641-662A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725186 | ||||||
| chr3:15725364
|
C | T | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-840G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725364 | ||||||
| chr3:15725380
|
C | T | 1 | a0001c0001t0002g0041 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.641-856G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725380 | ||||||
| chr3:15725453
|
C | T | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.641-929G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725453 | ||||||
| chr3:15725515
|
CATCTTGT others(12): Show |
C | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-1010_641-992de others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725515 | ||||||
| chr3:15725534
|
T | A | 6 | a0001c0002t0001g0134a0001c0002t0014g0109a0001c0002t0014g0110others(3): Show | 6 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-1010A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725534 | ||||||
| chr3:15725578
|
A | AT | 99 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.641-1055dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725578 | ||||||
| chr3:15725614
|
G | T | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.641-1090C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725614 | ||||||
| chr3:15725796
|
C | T | 132 | a0001c0001t0044g0178a0001c0002t0001g0112a0001c0002t0001g0113others(129): Show | 132 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.641-1272G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15725796 | ||||||
| chr3:15726095
|
C | T | 124 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(121): Show | 125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.641-1571G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726095 | ||||||
| chr3:15726257
|
G | T | 4 | a0001c0002t0001g0180a0001c0002t0001g0190a0001c0002t0022g0002others(1): Show | 4 | HG00639.hp2 HG02004.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-1733C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726257 | ||||||
| chr3:15726315
|
T | C | 12 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-1791A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726315 | ||||||
| chr3:15726317
|
G | C | 1 | a0001c0001t0003g0272 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.641-1793C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726317 | ||||||
| chr3:15726339
|
C | T | 277 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(274): Show | 278 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.641-1815G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726339 | ||||||
| chr3:15726349
|
TA | T | 90 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(87): Show | 91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.641-1826delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726349 | ||||||
| chr3:15726438
|
G | A | 1 | a0001c0002t0001g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.641-1914C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726438 | ||||||
| chr3:15726479
|
C | T | 1 | a0001c0002t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.641-1955G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726479 | ||||||
| chr3:15726580
|
T | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.641-2056A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726580 | ||||||
| chr3:15726584
|
G | C | 140 | a0001c0001t0044g0178a0001c0002t0001g0112a0001c0002t0001g0113others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.641-2060C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726584 | ||||||
| chr3:15726590
|
A | T | 140 | a0001c0001t0044g0178a0001c0002t0001g0112a0001c0002t0001g0113others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.641-2066T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726590 | ||||||
| chr3:15726618
|
G | A | 99 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.641-2094C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726618 | ||||||
| chr3:15726698
|
A | C | 6 | a0001c0002t0001g0216a0001c0002t0001g0217a0001c0002t0001g0218others(3): Show | 6 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-2174T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726698 | ||||||
| chr3:15726762
|
T | G | 3 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0032 | 3 | HG01934.hp1 HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.641-2238A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726762 | ||||||
| chr3:15726786
|
T | C | 279 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.641-2262A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726786 | ||||||
| chr3:15726812
|
C | T | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-2288G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726812 | ||||||
| chr3:15726820
|
C | G | 47 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.641-2296G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15726820 | ||||||
| chr3:15727019
|
AAAG | A | 6 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0036g0104others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-2498_641-2496d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727019 | ||||||
| chr3:15727072
|
C | A | 132 | a0001c0001t0044g0178a0001c0002t0001g0112a0001c0002t0001g0113others(129): Show | 132 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.641-2548G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727072 | ||||||
| chr3:15727241
|
T | C | 124 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(121): Show | 125 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.641-2717A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727241 | ||||||
| chr3:15727270
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.641-2746A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727270 | ||||||
| chr3:15727296
|
G | T | 1 | a0001c0002t0030g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.641-2772C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727296 | ||||||
| chr3:15727364
|
C | T | 1 | a0001c0002t0051g0279 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.641-2840G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727364 | ||||||
| chr3:15727403
|
C | A | 1 | a0001c0001t0002g0056 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.641-2879G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727403 | ||||||
| chr3:15727549
|
A | C | 2 | a0001c0001t0010g0274a0001c0001t0010g0275 | 2 | HG01934.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.641-3025T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727549 | ||||||
| chr3:15727564
|
C | CA | 22 | a0001c0001t0002g0023a0001c0001t0002g0080a0001c0001t0002g0084others(19): Show | 22 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.641-3041dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | ||||||
| chr3:15727564
|
C | CAA | 106 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(103): Show | 107 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.641-3042_641-3041d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | ||||||
| chr3:15727564
|
C | CAAA | 13 | a0001c0001t0002g0033a0001c0001t0002g0037a0001c0001t0002g0062others(10): Show | 13 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-3043_641-3041d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | ||||||
| chr3:15727564
|
CA | C | 17 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(14): Show | 17 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.641-3041delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | ||||||
| chr3:15727564
|
CAA | C | 121 | a0001c0001t0006g0314a0001c0002t0001g0112a0001c0002t0001g0113others(118): Show | 121 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.641-3042_641-3041d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | ||||||
| chr3:15727564
|
CAAA | C | 6 | a0001c0002t0001g0167a0001c0002t0001g0170a0001c0002t0001g0171others(3): Show | 6 | HG00099.hp2 HG02015.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.641-3043_641-3041d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727564 | ||||||
| chr3:15727583
|
A | G | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.641-3059T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727583 | ||||||
| chr3:15727587
|
A | G | 140 | a0001c0001t0044g0178a0001c0002t0001g0112a0001c0002t0001g0113others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.641-3063T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727587 | ||||||
| chr3:15727592
|
A | C | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.641-3068T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727592 | ||||||
| chr3:15727596
|
A | C | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-3072T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727596 | ||||||
| chr3:15727793
|
A | G | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-3269T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727793 | ||||||
| chr3:15727883
|
T | C | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-3359A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15727883 | ||||||
| chr3:15728012
|
A | C | 1 | a0001c0001t0002g0064 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.641-3488T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728012 | ||||||
| chr3:15728092
|
T | C | 1 | a0001c0002t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.641-3568A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728092 | ||||||
| chr3:15728104
|
C | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.641-3580G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728104 | ||||||
| chr3:15728108
|
A | G | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.641-3584T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728108 | ||||||
| chr3:15728153
|
AT | A | 14 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(11): Show | 14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.641-3630delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728153 | ||||||
| chr3:15728292
|
GTAAT | G | 237 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(234): Show | 238 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.641-3772_641-3769d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728292 | ||||||
| chr3:15728301
|
T | C | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-3777A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728301 | ||||||
| chr3:15728327
|
C | T | 2 | a0001c0001t0002g0013a0001c0001t0002g0014 | 2 | NA18983.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.641-3803G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728327 | ||||||
| chr3:15728385
|
C | G | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.641-3861G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15728385 | ||||||
| chr3:15729141
|
T | C | 293 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(290): Show | 294 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.641-4617A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729141 | ||||||
| chr3:15729165
|
G | A | 4 | a0001c0001t0002g0081a0001c0001t0002g0098a0001c0001t0002g0099others(1): Show | 4 | HG00621.hp1 HG02129.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-4641C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729165 | ||||||
| chr3:15729287
|
T | C | 1 | a0001c0001t0008g0337 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641-4763A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729287 | ||||||
| chr3:15729613
|
C | T | 4 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0160others(1): Show | 4 | NA18948.hp2 NA18954.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-5089G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729613 | ||||||
| chr3:15729709
|
T | G | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.641-5185A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729709 | ||||||
| chr3:15729784
|
G | C | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.641-5260C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729784 | ||||||
| chr3:15729842
|
T | C | 1 | a0001c0002t0001g0167 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.641-5318A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729842 | ||||||
| chr3:15729865
|
T | C | 279 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.641-5341A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729865 | ||||||
| chr3:15729902
|
A | T | 1 | a0001c0001t0002g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.641-5378T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15729902 | ||||||
| chr3:15730181
|
C | T | 1 | a0002c0006t0001g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.640+5229G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15730181 | ||||||
| chr3:15730653
|
C | T | 7 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0091others(4): Show | 7 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+4757G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15730653 | ||||||
| chr3:15730794
|
A | C | 48 | a0001c0001t0001g0166a0001c0002t0001g0112a0001c0002t0001g0113others(45): Show | 48 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.640+4616T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15730794 | ||||||
| chr3:15730799
|
G | A | 1 | a0001c0001t0008g0335 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.640+4611C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15730799 | ||||||
| chr3:15730827
|
T | C | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.640+4583A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15730827 | ||||||
| chr3:15731035
|
C | T | 1 | a0001c0007t0021g0303 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.640+4375G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731035 | ||||||
| chr3:15731141
|
A | G | 1 | a0001c0001t0002g0091 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.640+4269T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731141 | ||||||
| chr3:15731304
|
GA | G | 14 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(11): Show | 14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.640+4105delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731304 | ||||||
| chr3:15731314
|
GT | G | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+4095delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731314 | ||||||
| chr3:15731520
|
G | A | 1 | a0001c0001t0002g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.640+3890C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731520 | ||||||
| chr3:15731586
|
T | C | 1 | a0001c0001t0039g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.640+3824A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731586 | ||||||
| chr3:15731811
|
T | C | 6 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0036g0104others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+3599A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731811 | ||||||
| chr3:15731848
|
C | CA | 71 | a0001c0001t0002g0012a0001c0001t0002g0014a0001c0001t0002g0016others(68): Show | 71 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.640+3561dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | ||||||
| chr3:15731848
|
C | CAA | 9 | a0001c0001t0002g0020a0001c0001t0002g0038a0001c0001t0004g0245others(6): Show | 9 | HG02132.hp1 HG02486.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+3560_640+3561d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | ||||||
| chr3:15731848
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0006g0311a0001c0001t0006g0312a0001c0004t0009g0296others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+3554_640+3561d others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | ||||||
| chr3:15731848
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0307others(3): Show | 6 | HG01192.hp2 HG01884.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+3552_640+3561d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | ||||||
| chr3:15731848
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0006g0308 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.640+3551_640+3561d others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | ||||||
| chr3:15731848
|
C | CAAAAAAA others(5): Show |
1 | a0006c0012t0006g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.640+3550_640+3561d others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731848 | ||||||
| chr3:15731859
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.640+3535_640+3550d others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731859 | ||||||
| chr3:15731874
|
A | AAG | 22 | a0001c0001t0003g0266a0001c0001t0010g0275a0001c0002t0001g0168others(19): Show | 22 | HG00639.hp2 HG01243.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.640+3535_640+3536i others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731874 | ||||||
| chr3:15731874
|
A | AAGG | 7 | a0001c0002t0001g0132a0001c0002t0001g0167a0001c0002t0001g0172others(4): Show | 7 | NA18944.hp2 NA18965.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+3535_640+3536i others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731874 | ||||||
| chr3:15731874
|
A | G | 1 | a0001c0003t0005g0281 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.640+3536T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731874 | ||||||
| chr3:15731874
|
AG | A | 40 | a0001c0001t0002g0017a0001c0001t0002g0029a0001c0001t0002g0031others(37): Show | 40 | HG00408.hp1 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.640+3535delC | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731874 | ||||||
| chr3:15731875
|
G | A | 182 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(179): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.640+3535C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731875 | ||||||
| chr3:15731876
|
G | A | 109 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(106): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.640+3534C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731876 | ||||||
| chr3:15731877
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.640+3533C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731877 | ||||||
| chr3:15731882
|
G | T | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+3528C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731882 | ||||||
| chr3:15731883
|
G | T | 7 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0019others(4): Show | 7 | HG01099.hp1 HG01981.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+3527C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731883 | ||||||
| chr3:15731884
|
G | GT | 8 | a0001c0003t0005g0285a0001c0003t0005g0286a0001c0003t0005g0287others(5): Show | 8 | HG01168.hp2 HG02280.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.640+3525_640+3526i others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731884 | ||||||
| chr3:15731884
|
G | T | 9 | a0001c0003t0005g0281a0001c0003t0018g0232a0001c0003t0018g0233others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+3526C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15731884 | ||||||
| chr3:15732304
|
T | C | 1 | a0001c0002t0040g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.640+3106A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732304 | ||||||
| chr3:15732500
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.640+2910C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732500 | ||||||
| chr3:15732515
|
C | T | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.640+2895G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732515 | ||||||
| chr3:15732823
|
G | A | 4 | a0001c0001t0016g0327a0001c0001t0016g0328a0001c0001t0016g0330others(1): Show | 4 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2587C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732823 | ||||||
| chr3:15732840
|
A | T | 1 | a0001c0001t0004g0244 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.640+2570T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732840 | ||||||
| chr3:15732845
|
T | C | 1 | a0001c0002t0001g0224 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.640+2565A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732845 | ||||||
| chr3:15732937
|
G | A | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.640+2473C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15732937 | ||||||
| chr3:15733096
|
G | A | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.640+2314C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733096 | ||||||
| chr3:15733120
|
GTGCCGC | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0019others(1): Show | 4 | HG01099.hp1 HG01981.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2284_640+2289d others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733120 | ||||||
| chr3:15733271
|
A | G | 4 | a0001c0002t0001g0162a0001c0002t0001g0163a0001c0002t0001g0164others(1): Show | 4 | HG00673.hp1 NA18962.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2139T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733271 | ||||||
| chr3:15733287
|
G | A | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+2123C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733287 | ||||||
| chr3:15733318
|
A | G | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.640+2092T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733318 | ||||||
| chr3:15733388
|
T | A | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.640+2022A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733388 | ||||||
| chr3:15733418
|
G | A | 4 | a0001c0001t0002g0081a0001c0001t0002g0098a0001c0001t0002g0099others(1): Show | 4 | HG00621.hp1 HG02129.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+1992C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733418 | ||||||
| chr3:15733566
|
G | A | 1 | a0001c0001t0006g0305 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.640+1844C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733566 | ||||||
| chr3:15733661
|
T | C | 3 | a0001c0001t0010g0276a0001c0001t0010g0277a0001c0001t0010g0278 | 3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.640+1749A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733661 | ||||||
| chr3:15733766
|
C | T | 1 | a0001c0001t0015g0325 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.640+1644G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733766 | ||||||
| chr3:15733909
|
A | G | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.640+1501T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733909 | ||||||
| chr3:15733918
|
T | C | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.640+1492A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733918 | ||||||
| chr3:15733939
|
T | C | 2 | a0001c0002t0001g0200a0001c0002t0001g0201 | 2 | HG02735.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.640+1471A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733939 | ||||||
| chr3:15733955
|
T | C | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.640+1455A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15733955 | ||||||
| chr3:15734012
|
C | G | 1 | a0005c0011t0003g0255 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.640+1398G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734012 | ||||||
| chr3:15734087
|
T | C | 8 | a0001c0001t0002g0011a0001c0001t0002g0033a0001c0001t0002g0034others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+1323A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734087 | ||||||
| chr3:15734090
|
A | G | 2 | a0001c0002t0001g0134a0001c0002t0042g0133 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.640+1320T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734090 | ||||||
| chr3:15734094
|
T | A | 2 | a0001c0002t0001g0134a0001c0002t0042g0133 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.640+1316A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734094 | ||||||
| chr3:15734142
|
T | C | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.640+1268A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734142 | ||||||
| chr3:15734187
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.640+1223A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734187 | ||||||
| chr3:15734191
|
G | T | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.640+1219C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734191 | ||||||
| chr3:15734265
|
C | T | 7 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0245others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+1145G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734265 | ||||||
| chr3:15734280
|
C | T | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.640+1130G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734280 | ||||||
| chr3:15734337
|
G | A | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.640+1073C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734337 | ||||||
| chr3:15734357
|
C | A | 1 | a0001c0002t0014g0110 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.640+1053G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734357 | ||||||
| chr3:15734361
|
T | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.640+1049A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734361 | ||||||
| chr3:15734376
|
C | A | 1 | a0001c0001t0016g0328 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.640+1034G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734376 | ||||||
| chr3:15734456
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.640+954A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734456 | ||||||
| chr3:15734516
|
A | G | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+894T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734516 | ||||||
| chr3:15734667
|
C | T | 1 | a0001c0002t0011g0237 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.640+743G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734667 | ||||||
| chr3:15734686
|
T | G | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.640+724A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734686 | ||||||
| chr3:15734719
|
C | T | 1 | a0001c0002t0030g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.640+691G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734719 | ||||||
| chr3:15734913
|
CTG | C | 238 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(235): Show | 239 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.640+495_640+496del others(2): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15734913 | ||||||
| chr3:15735017
|
G | A | 254 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(251): Show | 255 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.640+393C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15735017 | ||||||
| chr3:15735177
|
A | G | 238 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(235): Show | 239 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.640+233T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 6/27 | chr3 | 15735177 | ||||||
| chr3:15735643
|
G | A | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-146C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15735643 | ||||||
| chr3:15735838
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.553-341G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15735838 | ||||||
| chr3:15735840
|
T | C | 3 | a0001c0002t0001g0194a0001c0002t0001g0204a0001c0002t0001g0205 | 3 | HG00733.hp2 HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.553-343A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15735840 | ||||||
| chr3:15735916
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.553-419C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15735916 | ||||||
| chr3:15735982
|
A | G | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-485T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15735982 | ||||||
| chr3:15736232
|
T | C | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.553-735A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15736232 | ||||||
| chr3:15736284
|
C | T | 2 | a0001c0002t0001g0112a0001c0002t0001g0113 | 2 | NA19063.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.552+749G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15736284 | ||||||
| chr3:15736353
|
G | C | 2 | a0001c0001t0002g0067a0004c0008t0002g0088 | 2 | HG02071.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.552+680C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15736353 | ||||||
| chr3:15736454
|
C | T | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+579G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 5/27 | chr3 | 15736454 | ||||||
| chr3:15737276
|
T | C | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352-43A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737276 | ||||||
| chr3:15737312
|
G | T | 12 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.352-79C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737312 | ||||||
| chr3:15737375
|
A | T | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-142T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737375 | ||||||
| chr3:15737521
|
A | AAAAGAAA others(137): Show |
1 | a0001c0002t0030g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.352-289_352-288ins others(144): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737521 | ||||||
| chr3:15737522
|
G | GAAGAAAT others(137): Show |
279 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(276): Show | 280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.352-290_352-289ins others(144): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737522 | ||||||
| chr3:15737522
|
G | T | 1 | a0001c0002t0030g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.352-289C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737522 | ||||||
| chr3:15737608
|
G | C | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352-375C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737608 | ||||||
| chr3:15737687
|
C | A | 254 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(251): Show | 255 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.352-454G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737687 | ||||||
| chr3:15737707
|
C | T | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.352-474G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737707 | ||||||
| chr3:15737899
|
TA | T | 209 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0017others(206): Show | 209 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.352-667delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737899 | ||||||
| chr3:15737925
|
G | A | 1 | a0001c0001t0002g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.352-692C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15737925 | ||||||
| chr3:15738162
|
C | T | 1 | a0001c0002t0001g0183 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.352-929G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738162 | ||||||
| chr3:15738163
|
G | A | 21 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.352-930C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738163 | ||||||
| chr3:15738304
|
G | A | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.352-1071C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738304 | ||||||
| chr3:15738349
|
G | C | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-1116C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738349 | ||||||
| chr3:15738350
|
T | A | 1 | a0001c0002t0001g0221 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.352-1117A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738350 | ||||||
| chr3:15738355
|
G | A | 15 | a0001c0002t0001g0180a0001c0002t0001g0181a0001c0002t0001g0190others(12): Show | 15 | HG00639.hp2 HG02004.hp1 HG02273.hp2 others(12): Show |
intron_variant | MODIFIER | c.352-1122C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738355 | ||||||
| chr3:15738531
|
C | T | 1 | a0001c0003t0005g0287 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.352-1298G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738531 | ||||||
| chr3:15738576
|
G | A | 1 | a0001c0001t0016g0330 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.352-1343C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738576 | ||||||
| chr3:15738588
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.352-1355C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738588 | ||||||
| chr3:15738608
|
C | G | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.352-1375G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738608 | ||||||
| chr3:15738660
|
G | A | 3 | a0001c0001t0002g0018a0001c0002t0030g0010a0001c0014t0037g0105 | 3 | HG01993.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.352-1427C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738660 | ||||||
| chr3:15738665
|
C | A | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-1432G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738665 | ||||||
| chr3:15738770
|
A | T | 1 | a0001c0001t0059g0333 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.352-1537T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738770 | ||||||
| chr3:15738875
|
A | G | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-1642T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738875 | ||||||
| chr3:15738911
|
T | C | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.352-1678A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15738911 | ||||||
| chr3:15739016
|
T | C | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-1783A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739016 | ||||||
| chr3:15739082
|
T | C | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-1849A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739082 | ||||||
| chr3:15739149
|
T | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-1916A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739149 | ||||||
| chr3:15739429
|
C | T | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.352-2196G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739429 | ||||||
| chr3:15739498
|
C | T | 238 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(235): Show | 239 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.352-2265G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739498 | ||||||
| chr3:15739652
|
A | C | 2 | a0001c0003t0018g0232a0001c0003t0018g0233 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.352-2419T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739652 | ||||||
| chr3:15739776
|
A | T | 1 | a0001c0002t0001g0196 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.352-2543T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739776 | ||||||
| chr3:15739797
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.352-2564T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739797 | ||||||
| chr3:15739848
|
C | T | 1 | a0001c0002t0001g0208 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.352-2615G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739848 | ||||||
| chr3:15739853
|
G | A | 2 | a0001c0001t0003g0258a0001c0005t0012g0318 | 2 | HG03209.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.352-2620C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15739853 | ||||||
| chr3:15740029
|
TAAAC | T | 6 | a0001c0002t0001g0134a0001c0002t0014g0109a0001c0002t0014g0110others(3): Show | 6 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-2800_352-2797d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740029 | ||||||
| chr3:15740113
|
G | C | 238 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(235): Show | 239 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.352-2880C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740113 | ||||||
| chr3:15740298
|
A | C | 99 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.352-3065T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740298 | ||||||
| chr3:15740304
|
C | T | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-3071G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740304 | ||||||
| chr3:15740357
|
A | G | 6 | a0001c0002t0001g0134a0001c0002t0014g0109a0001c0002t0014g0110others(3): Show | 6 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-3124T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740357 | ||||||
| chr3:15740552
|
G | C | 2 | a0001c0002t0001g0167a0001c0002t0001g0168 | 2 | NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.352-3319C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740552 | ||||||
| chr3:15740667
|
C | T | 254 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(251): Show | 255 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.352-3434G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740667 | ||||||
| chr3:15740831
|
C | T | 5 | a0001c0002t0007g0174a0001c0002t0007g0175a0001c0002t0007g0176others(2): Show | 5 | NA18944.hp2 NA18950.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-3598G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740831 | ||||||
| chr3:15740834
|
T | G | 3 | a0001c0002t0001g0119a0001c0002t0001g0120a0001c0002t0001g0121 | 3 | HG01978.hp1 HG02148.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.352-3601A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740834 | ||||||
| chr3:15740928
|
C | T | 4 | a0001c0001t0002g0061a0001c0001t0010g0276a0001c0001t0010g0277others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-3695G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740928 | ||||||
| chr3:15740995
|
T | G | 1 | a0001c0001t0002g0021 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.352-3762A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15740995 | ||||||
| chr3:15741025
|
C | T | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352-3792G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741025 | ||||||
| chr3:15741042
|
T | A | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-3809A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741042 | ||||||
| chr3:15741060
|
G | A | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02615.hp2 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.352-3827C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741060 | ||||||
| chr3:15741068
|
G | A | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.352-3835C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741068 | ||||||
| chr3:15741143
|
G | A | 1 | a0001c0002t0017g0227 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.352-3910C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741143 | ||||||
| chr3:15741198
|
CAAAAAAA | C | 48 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(45): Show | 49 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.352-3972_352-3966d others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741198 | ||||||
| chr3:15741204
|
A | C | 184 | a0001c0001t0001g0166a0001c0001t0002g0055a0001c0001t0002g0056others(181): Show | 184 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.352-3971T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741204 | ||||||
| chr3:15741205
|
A | C | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-3972T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741205 | ||||||
| chr3:15741424
|
C | T | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.352-4191G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741424 | ||||||
| chr3:15741697
|
C | CTTTTTT | 7 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0311others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.352-4470_352-4465d others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0006g0314a0001c0004t0009g0296 | 2 | HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.352-4474_352-4465d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0004g0238a0001c0001t0004g0239 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.352-4476_352-4465d others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
C | CTTTTTTT others(6): Show |
2 | a0001c0003t0053g0313a0001c0004t0009g0297 | 2 | HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.352-4477_352-4465d others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0004g0248 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.352-4481_352-4465d others(19): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0004g0247 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.352-4482_352-4465d others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CT | C | 16 | a0001c0001t0003g0254a0001c0001t0003g0256a0001c0001t0003g0258others(13): Show | 16 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-4465delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTT | C | 14 | a0001c0001t0003g0272a0001c0001t0008g0334a0001c0001t0008g0338others(11): Show | 14 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.352-4466_352-4465d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTT | C | 14 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0041others(11): Show | 14 | HG01168.hp2 HG01433.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.352-4467_352-4465d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTT | C | 31 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0016others(28): Show | 32 | HG00423.hp2 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.352-4468_352-4465d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTT | C | 37 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(34): Show | 37 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.352-4469_352-4465d others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTT | C | 13 | a0001c0002t0001g0116a0001c0002t0001g0118a0001c0002t0001g0183others(10): Show | 13 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.352-4470_352-4465d others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT | C | 9 | a0001c0001t0001g0166a0001c0001t0004g0246a0001c0002t0001g0124others(6): Show | 9 | HG00738.hp2 HG02602.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-4471_352-4465d others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(1): Show |
C | 22 | a0001c0001t0006g0309a0001c0001t0044g0178a0001c0002t0001g0120others(19): Show | 22 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.352-4472_352-4465d others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(2): Show |
C | 65 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(62): Show | 65 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.352-4473_352-4465d others(11): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(3): Show |
C | 8 | a0001c0002t0001g0150a0001c0002t0001g0158a0001c0002t0001g0167others(5): Show | 8 | HG00621.hp2 HG02965.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-4474_352-4465d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0245 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.352-4475_352-4465d others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0002g0055a0001c0001t0002g0071a0001c0001t0002g0078others(3): Show | 6 | HG00597.hp2 HG01884.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.352-4479_352-4465d others(17): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(9): Show |
C | 44 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(41): Show | 44 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.352-4480_352-4465d others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(10): Show |
C | 5 | a0001c0001t0002g0076a0001c0001t0002g0080a0001c0001t0002g0082others(2): Show | 5 | HG01069.hp2 HG03490.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-4481_352-4465d others(19): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0002t0001g0170 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.352-4483_352-4465d others(21): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(13): Show |
C | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.352-4484_352-4465d others(22): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0002g0038a0001c0001t0004g0252 | 2 | HG03225.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.352-4485_352-4465d others(23): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(15): Show |
C | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352-4486_352-4465d others(24): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741697
|
CTTTTTTT others(19): Show |
C | 6 | a0001c0001t0004g0240a0001c0001t0004g0241a0001c0001t0004g0242others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.352-4490_352-4465d others(28): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741697 | ||||||
| chr3:15741848
|
T | C | 3 | a0001c0004t0009g0298a0001c0004t0009g0299a0001c0004t0025g0005 | 3 | HG02723.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.352-4615A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741848 | ||||||
| chr3:15741865
|
T | C | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-4632A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741865 | ||||||
| chr3:15741874
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.352-4641A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741874 | ||||||
| chr3:15741881
|
C | T | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.352-4648G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741881 | ||||||
| chr3:15741883
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.352-4650G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741883 | ||||||
| chr3:15741893
|
C | T | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-4660G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741893 | ||||||
| chr3:15741935
|
C | T | 2 | a0001c0002t0001g0195a0001c0002t0001g0198 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.352-4702G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741935 | ||||||
| chr3:15741948
|
G | A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.352-4715C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741948 | ||||||
| chr3:15741964
|
C | G | 232 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.352-4731G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15741964 | ||||||
| chr3:15742011
|
T | C | 14 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(11): Show | 14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.352-4778A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742011 | ||||||
| chr3:15742019
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.352-4786C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742019 | ||||||
| chr3:15742089
|
A | G | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-4856T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742089 | ||||||
| chr3:15742126
|
G | A | 2 | a0001c0002t0001g0167a0001c0002t0001g0168 | 2 | NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.352-4893C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742126 | ||||||
| chr3:15742157
|
A | AC | 4 | a0001c0001t0002g0075a0001c0002t0001g0112a0001c0002t0001g0194others(1): Show | 4 | HG00738.hp1 HG00741.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-4925dupG | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742157 | ||||||
| chr3:15742180
|
G | A | 243 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(240): Show | 244 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.352-4947C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742180 | ||||||
| chr3:15742194
|
G | A | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.352-4961C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742194 | ||||||
| chr3:15742195
|
C | T | 3 | a0001c0002t0001g0194a0001c0002t0001g0204a0001c0002t0001g0205 | 3 | HG00733.hp2 HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.352-4962G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742195 | ||||||
| chr3:15742269
|
C | T | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-5036G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742269 | ||||||
| chr3:15742356
|
C | T | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-5123G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742356 | ||||||
| chr3:15742357
|
G | A | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.352-5124C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742357 | ||||||
| chr3:15742389
|
G | A | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.352-5156C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742389 | ||||||
| chr3:15742394
|
G | A | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.352-5161C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742394 | ||||||
| chr3:15742408
|
A | G | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.352-5175T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742408 | ||||||
| chr3:15742411
|
C | T | 1 | a0001c0001t0003g0272 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.352-5178G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742411 | ||||||
| chr3:15742428
|
G | A | 23 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.352-5195C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742428 | ||||||
| chr3:15742434
|
G | A | 1 | a0001c0005t0057g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.352-5201C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742434 | ||||||
| chr3:15742465
|
C | T | 3 | a0001c0002t0001g0194a0001c0002t0001g0204a0001c0002t0001g0205 | 3 | HG00733.hp2 HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.352-5232G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742465 | ||||||
| chr3:15742470
|
C | T | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.352-5237G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742470 | ||||||
| chr3:15742471
|
G | A | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.352-5238C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742471 | ||||||
| chr3:15742506
|
G | A | 48 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(45): Show | 49 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.352-5273C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742506 | ||||||
| chr3:15742515
|
G | A | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352-5282C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742515 | ||||||
| chr3:15742534
|
C | T | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352-5301G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742534 | ||||||
| chr3:15742538
|
C | T | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-5305G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742538 | ||||||
| chr3:15742579
|
A | G | 1 | a0001c0001t0006g0309 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.352-5346T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742579 | ||||||
| chr3:15742594
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.352-5361G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742594 | ||||||
| chr3:15742595
|
G | A | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-5362C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742595 | ||||||
| chr3:15742614
|
G | A | 40 | a0001c0001t0002g0027a0001c0001t0002g0055a0001c0001t0002g0056others(37): Show | 40 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.352-5381C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742614 | ||||||
| chr3:15742619
|
CT | C | 337 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(334): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.352-5387delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742619 | ||||||
| chr3:15742621
|
G | A | 6 | a0001c0002t0001g0115a0001c0002t0001g0132a0001c0002t0001g0172others(3): Show | 6 | NA18747.hp2 NA18965.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-5388C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742621 | ||||||
| chr3:15742624
|
A | C | 1 | a0001c0001t0002g0079 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5391T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742624 | ||||||
| chr3:15742625
|
G | A | 1 | a0001c0001t0002g0079 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5392C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742625 | ||||||
| chr3:15742659
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5426T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742659 | ||||||
| chr3:15742669
|
T | C | 1 | a0001c0001t0002g0079 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5436A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742669 | ||||||
| chr3:15742671
|
C | CCCGGCCA others(693): Show |
1 | a0001c0001t0002g0079 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5439_352-5438i others(702): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742671 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
1 | a0001c0005t0012g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
4 | a0001c0005t0012g0319a0001c0005t0057g0323a0001c0010t0012g0316others(1): Show | 4 | HG02622.hp1 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
3 | a0001c0002t0011g0236a0001c0002t0011g0237a0003c0015t0011g0234 | 3 | HG01255.hp1 HG01993.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(746): Show |
1 | a0001c0001t0008g0338 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(755): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
1 | a0001c0001t0002g0021 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(729): Show |
1 | a0001c0003t0005g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(738): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(792): Show |
1 | a0001c0003t0053g0313 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(801): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(791): Show |
10 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(791): Show |
1 | a0001c0004t0009g0298 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(792): Show |
1 | a0001c0001t0006g0309 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(801): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(791): Show |
2 | a0001c0001t0006g0311a0001c0001t0006g0312 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(791): Show |
8 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
2 | a0001c0001t0002g0055a0001c0001t0029g0009 | 2 | NA18954.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(744): Show |
3 | a0001c0001t0004g0244a0001c0001t0004g0245a0001c0001t0004g0246 | 3 | HG02258.hp2 HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(753): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
1 | a0001c0001t0015g0325 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
12 | a0001c0001t0003g0261a0001c0001t0004g0238a0001c0001t0004g0239others(9): Show | 12 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(731): Show |
1 | a0001c0003t0005g0287 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(740): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(747): Show |
1 | a0001c0001t0002g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(756): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(744): Show |
1 | a0001c0002t0001g0220 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(753): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(745): Show |
1 | a0001c0002t0017g0227 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(754): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
3 | a0001c0001t0002g0042a0001c0002t0017g0228a0004c0008t0002g0088 | 3 | NA18956.hp1 NA18998.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(744): Show |
1 | a0001c0002t0051g0279 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(753): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
5 | a0001c0002t0001g0121a0001c0002t0001g0204a0001c0002t0001g0219others(2): Show | 5 | HG00741.hp2 HG01978.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
2 | a0001c0001t0008g0334a0001c0001t0008g0339 | 2 | NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
7 | a0001c0001t0015g0324a0001c0001t0015g0326a0001c0001t0016g0327others(4): Show | 7 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
3 | a0001c0001t0008g0335a0001c0001t0008g0336a0001c0001t0008g0337 | 3 | HG02896.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0001t0008g0332 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0002t0001g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0002t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
26 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0003g0256others(23): Show | 26 | HG00099.hp1 HG00733.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0001t0010g0274 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
1 | a0001c0001t0002g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
1 | a0001c0002t0041g0169 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(729): Show |
1 | a0001c0009t0005g0284 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(738): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(744): Show |
1 | a0004c0008t0002g0043 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(753): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0001t0002g0092 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
1 | a0001c0001t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
86 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 87 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(728): Show |
8 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(737): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(728): Show |
1 | a0001c0003t0005g0292 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(737): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0002t0001g0147 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
1 | a0001c0002t0042g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(743): Show |
1 | a0001c0002t0001g0194 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(752): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
110 | a0001c0001t0001g0166a0001c0002t0001g0112a0001c0002t0001g0113others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(693): Show |
1 | a0001c0002t0038g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(702): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0001t0002g0097 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
2 | a0001c0002t0001g0214a0001c0002t0001g0225 | 2 | HG01081.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0001t0044g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(791): Show |
2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCC others(742): Show |
1 | a0001c0001t0003g0272 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(751): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | AGCCAGCT others(791): Show |
1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352-5442_352-5441i others(800): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742674
|
A | C | 1 | a0001c0001t0002g0079 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5441T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742674 | ||||||
| chr3:15742675
|
T | G | 338 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.352-5442A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742675 | ||||||
| chr3:15742683
|
T | G | 338 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.352-5450A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742683 | ||||||
| chr3:15742684
|
G | C | 338 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.352-5451C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742684 | ||||||
| chr3:15742688
|
G | A | 338 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.352-5455C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742688 | ||||||
| chr3:15742736
|
C | T | 1 | a0001c0001t0002g0079 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.352-5503G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742736 | ||||||
| chr3:15742769
|
G | A | 2 | a0001c0001t0004g0238a0001c0001t0004g0239 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.352-5536C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742769 | ||||||
| chr3:15742773
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.352-5540C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742773 | ||||||
| chr3:15742781
|
A | G | 264 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(261): Show | 265 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.352-5548T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742781 | ||||||
| chr3:15742803
|
C | T | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-5570G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742803 | ||||||
| chr3:15742814
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.352-5581C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742814 | ||||||
| chr3:15742817
|
C | T | 2 | a0001c0002t0001g0171a0001c0002t0001g0218 | 2 | HG02015.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.352-5584G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742817 | ||||||
| chr3:15742897
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.352-5664C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742897 | ||||||
| chr3:15742900
|
C | T | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-5667G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742900 | ||||||
| chr3:15742909
|
C | T | 3 | a0001c0007t0021g0302a0001c0007t0021g0303a0003c0013t0052g0293 | 3 | HG01884.hp2 NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-5676G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742909 | ||||||
| chr3:15742915
|
T | C | 5 | a0001c0005t0020g0300a0001c0005t0020g0301a0001c0007t0021g0302others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-5682A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742915 | ||||||
| chr3:15742996
|
T | A | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-5763A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15742996 | ||||||
| chr3:15743355
|
A | AAAAC | 9 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0138others(6): Show | 9 | HG00642.hp1 HG01071.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-6126_352-6123d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743355 | ||||||
| chr3:15743370
|
ACAAAC | A | 3 | a0001c0007t0021g0302a0001c0007t0021g0303a0003c0013t0052g0293 | 3 | HG01884.hp2 NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.352-6142_352-6138d others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743370 | ||||||
| chr3:15743375
|
C | A | 1 | a0001c0001t0013g0001 | 2 | NA18945.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.352-6142G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743375 | ||||||
| chr3:15743375
|
C | CA | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-6143dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743375 | ||||||
| chr3:15743384
|
A | C | 232 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(229): Show | 233 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.352-6151T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743384 | ||||||
| chr3:15743539
|
C | T | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-6306G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743539 | ||||||
| chr3:15743545
|
A | AAC | 16 | a0001c0001t0002g0020a0001c0001t0002g0072a0001c0001t0002g0075others(13): Show | 16 | HG00733.hp1 HG01099.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.352-6314_352-6313d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | ||||||
| chr3:15743545
|
A | AACAC | 4 | a0001c0001t0002g0071a0001c0002t0001g0120a0001c0002t0001g0197others(1): Show | 4 | HG00642.hp2 HG01192.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-6316_352-6313d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | ||||||
| chr3:15743545
|
A | AACACACA others(9): Show |
1 | a0002c0006t0001g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.352-6328_352-6313d others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | ||||||
| chr3:15743545
|
AAC | A | 80 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.352-6314_352-6313d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | ||||||
| chr3:15743545
|
AACAC | A | 61 | a0001c0001t0002g0022a0001c0001t0002g0051a0001c0001t0002g0052others(58): Show | 61 | HG00639.hp2 HG00738.hp2 HG01891.hp1 others(58): Show |
intron_variant | MODIFIER | c.352-6316_352-6313d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | ||||||
| chr3:15743545
|
AACACAC | A | 32 | a0001c0001t0002g0011a0001c0001t0002g0016a0001c0001t0002g0018others(29): Show | 33 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.352-6318_352-6313d others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | ||||||
| chr3:15743545
|
AACACACA others(1): Show |
A | 41 | a0001c0001t0001g0166a0001c0001t0002g0012a0001c0001t0002g0019others(38): Show | 41 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.352-6320_352-6313d others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | ||||||
| chr3:15743545
|
AACACACA others(3): Show |
A | 4 | a0001c0001t0002g0032a0001c0001t0002g0037a0001c0002t0001g0141others(1): Show | 4 | HG01891.hp2 HG02293.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-6322_352-6313d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | ||||||
| chr3:15743545
|
AACACACA others(7): Show |
A | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.352-6326_352-6313d others(16): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743545 | ||||||
| chr3:15743580
|
A | ACACACAC others(9): Show |
2 | a0001c0003t0005g0281a0001c0003t0005g0282 | 2 | HG01109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.352-6348_352-6347i others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743580 | ||||||
| chr3:15743580
|
A | ACACACAC others(5): Show |
1 | a0001c0003t0005g0287 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.352-6348_352-6347i others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743580 | ||||||
| chr3:15743580
|
A | ACACACAC others(3): Show |
3 | a0001c0003t0005g0289a0001c0003t0005g0292a0001c0009t0005g0284 | 3 | HG02055.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.352-6348_352-6347i others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743580 | ||||||
| chr3:15743580
|
A | ACACACAC others(1): Show |
5 | a0001c0003t0005g0285a0001c0003t0005g0286a0001c0003t0005g0288others(2): Show | 5 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-6348_352-6347i others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743580 | ||||||
| chr3:15743580
|
A | G | 1 | a0001c0001t0004g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.352-6347T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743580 | ||||||
| chr3:15743582
|
ACACACAC others(10): Show |
A | 1 | a0001c0001t0004g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.352-6366_352-6350d others(19): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743582 | ||||||
| chr3:15743593
|
C | T | 2 | a0001c0001t0003g0254a0001c0001t0003g0261 | 2 | HG01167.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.352-6360G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743593 | ||||||
| chr3:15743645
|
G | A | 2 | a0001c0001t0003g0253a0001c0001t0003g0271 | 2 | HG00733.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.352-6412C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743645 | ||||||
| chr3:15743679
|
T | C | 1 | a0001c0001t0002g0025 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.352-6446A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743679 | ||||||
| chr3:15743749
|
G | A | 1 | a0001c0005t0012g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.352-6516C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743749 | ||||||
| chr3:15743827
|
C | T | 1 | a0001c0002t0001g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.352-6594G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15743827 | ||||||
| chr3:15744046
|
G | C | 2 | a0001c0001t0002g0086a0001c0001t0033g0101 | 2 | NA18952.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.352-6813C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744046 | ||||||
| chr3:15744148
|
T | C | 42 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.352-6915A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744148 | ||||||
| chr3:15744251
|
T | G | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.352-7018A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744251 | ||||||
| chr3:15744406
|
C | A | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-7173G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744406 | ||||||
| chr3:15744455
|
G | A | 1 | a0001c0001t0010g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.352-7222C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744455 | ||||||
| chr3:15744473
|
C | CT | 111 | a0001c0001t0002g0018a0001c0001t0002g0033a0001c0001t0002g0070others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(108): Show |
intron_variant | MODIFIER | c.352-7241dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744473 | ||||||
| chr3:15744473
|
C | CTT | 97 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(94): Show | 98 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.352-7242_352-7241d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744473 | ||||||
| chr3:15744597
|
G | A | 1 | a0001c0002t0007g0184 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.351+7153C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744597 | ||||||
| chr3:15744623
|
G | A | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.351+7127C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744623 | ||||||
| chr3:15744664
|
T | G | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.351+7086A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744664 | ||||||
| chr3:15744771
|
G | A | 1 | a0001c0001t0039g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.351+6979C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744771 | ||||||
| chr3:15744774
|
T | C | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.351+6976A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15744774 | ||||||
| chr3:15745046
|
T | C | 1 | a0001c0002t0001g0145 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.351+6704A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745046 | ||||||
| chr3:15745151
|
T | C | 4 | a0001c0001t0002g0091a0001c0001t0002g0094a0001c0001t0002g0095others(1): Show | 4 | HG02886.hp2 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+6599A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745151 | ||||||
| chr3:15745621
|
A | G | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+6129T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745621 | ||||||
| chr3:15745667
|
G | C | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.351+6083C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745667 | ||||||
| chr3:15745721
|
A | G | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+6029T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745721 | ||||||
| chr3:15745722
|
ATT | A | 30 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0118others(27): Show | 30 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.351+6026_351+6027d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745722 | ||||||
| chr3:15745777
|
C | T | 19 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(16): Show | 19 | HG01109.hp2 HG01168.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+5973G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745777 | ||||||
| chr3:15745785
|
G | A | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+5965C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745785 | ||||||
| chr3:15745805
|
T | A | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+5945A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745805 | ||||||
| chr3:15745836
|
C | T | 1 | a0001c0002t0014g0110 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.351+5914G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15745836 | ||||||
| chr3:15746042
|
T | C | 3 | a0001c0002t0001g0159a0001c0002t0001g0185a0001c0002t0001g0186 | 3 | HG00558.hp1 NA19000.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.351+5708A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746042 | ||||||
| chr3:15746333
|
C | T | 294 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(291): Show | 295 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.351+5417G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746333 | ||||||
| chr3:15746379
|
T | A | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+5371A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746379 | ||||||
| chr3:15746388
|
T | C | 1 | a0001c0003t0018g0233 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.351+5362A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746388 | ||||||
| chr3:15746405
|
G | A | 1 | a0001c0005t0057g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.351+5345C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746405 | ||||||
| chr3:15746491
|
G | C | 1 | a0001c0002t0046g0153 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.351+5259C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746491 | ||||||
| chr3:15746528
|
T | C | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+5222A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746528 | ||||||
| chr3:15746550
|
C | T | 1 | a0001c0001t0004g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.351+5200G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746550 | ||||||
| chr3:15746631
|
A | C | 1 | a0001c0002t0043g0122 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.351+5119T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746631 | ||||||
| chr3:15746985
|
A | G | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+4765T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15746985 | ||||||
| chr3:15747166
|
CT | C | 27 | a0001c0001t0002g0052a0001c0001t0002g0054a0001c0001t0016g0327others(24): Show | 27 | HG00140.hp1 HG01109.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.351+4583delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747166 | ||||||
| chr3:15747198
|
T | C | 42 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.351+4552A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747198 | ||||||
| chr3:15747406
|
T | C | 1 | a0001c0002t0051g0279 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.351+4344A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747406 | ||||||
| chr3:15747447
|
G | T | 47 | a0001c0001t0001g0166a0001c0002t0001g0112a0001c0002t0001g0113others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.351+4303C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747447 | ||||||
| chr3:15747457
|
C | T | 1 | a0001c0001t0003g0272 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.351+4293G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747457 | ||||||
| chr3:15747463
|
C | G | 1 | a0001c0005t0057g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.351+4287G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747463 | ||||||
| chr3:15747474
|
GTTATTTA others(3): Show |
G | 1 | a0001c0002t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.351+4266_351+4275d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747474 | ||||||
| chr3:15747564
|
A | G | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.351+4186T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747564 | ||||||
| chr3:15747735
|
C | T | 131 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.351+4015G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747735 | ||||||
| chr3:15747836
|
G | A | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.351+3914C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747836 | ||||||
| chr3:15747881
|
G | C | 1 | a0001c0001t0002g0031 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.351+3869C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747881 | ||||||
| chr3:15747939
|
A | T | 1 | a0001c0002t0001g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.351+3811T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747939 | ||||||
| chr3:15747971
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.351+3779C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15747971 | ||||||
| chr3:15748063
|
T | A | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+3687A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748063 | ||||||
| chr3:15748128
|
T | G | 1 | a0001c0001t0002g0054 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.351+3622A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748128 | ||||||
| chr3:15748130
|
A | T | 1 | a0001c0001t0002g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.351+3620T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748130 | ||||||
| chr3:15748193
|
T | C | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+3557A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748193 | ||||||
| chr3:15748208
|
G | A | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.351+3542C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748208 | ||||||
| chr3:15748215
|
A | G | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+3535T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748215 | ||||||
| chr3:15748489
|
C | T | 280 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(277): Show | 281 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.351+3261G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748489 | ||||||
| chr3:15748547
|
C | T | 1 | a0001c0002t0046g0153 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.351+3203G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748547 | ||||||
| chr3:15748663
|
T | C | 1 | a0001c0002t0001g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.351+3087A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748663 | ||||||
| chr3:15748895
|
A | T | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0024others(2): Show | 5 | HG00597.hp1 NA18956.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+2855T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748895 | ||||||
| chr3:15748896
|
T | A | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+2854A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748896 | ||||||
| chr3:15748951
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.351+2799C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748951 | ||||||
| chr3:15748992
|
T | G | 1 | a0001c0005t0012g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.351+2758A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15748992 | ||||||
| chr3:15749093
|
A | ATGTTTTT others(1): Show |
37 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(34): Show | 38 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.351+2656_351+2657i others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749093 | ||||||
| chr3:15749095
|
G | GT | 11 | a0001c0001t0004g0246a0001c0001t0006g0315a0001c0002t0030g0010others(8): Show | 11 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.351+2654dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTT | 7 | a0001c0003t0005g0281a0001c0003t0005g0285a0001c0003t0005g0286others(4): Show | 7 | HG01168.hp2 HG02055.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+2653_351+2654d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTTT | 7 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0003t0005g0282others(4): Show | 7 | HG01109.hp2 HG02129.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+2652_351+2654d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTTTTTTT others(2): Show |
9 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0044others(6): Show | 9 | HG01433.hp2 HG03195.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+2654_351+2655i others(11): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTTTTTTT others(3): Show |
1 | a0001c0002t0017g0227 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.351+2654_351+2655i others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTTTTTTT others(2): Show |
17 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0061others(14): Show | 17 | HG00408.hp1 HG01069.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.351+2654_351+2655i others(11): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTTTTTTT others(3): Show |
13 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0060others(10): Show | 13 | HG02040.hp1 HG02523.hp2 HG03239.hp1 others(10): Show |
intron_variant | MODIFIER | c.351+2654_351+2655i others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTTTTTTT others(4): Show |
11 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0067others(8): Show | 11 | HG02071.hp2 NA18747.hp1 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.351+2654_351+2655i others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTTTTTTT others(5): Show |
5 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0065others(2): Show | 5 | HG00597.hp2 HG00673.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2654_351+2655i others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0057 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.351+2654_351+2655i others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTTTTTTT others(7): Show |
2 | a0001c0001t0002g0081a0001c0001t0002g0087 | 2 | HG00621.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.351+2654_351+2655i others(16): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | GTTTTTTT others(11): Show |
1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.351+2654_351+2655i others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
G | T | 1 | a0001c0001t0002g0079 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.351+2655C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
GTTTTTGT | G | 29 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0134others(26): Show | 29 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.351+2648_351+2654d others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749095
|
GTTTTTGT others(1): Show |
G | 97 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(94): Show | 97 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.351+2647_351+2654d others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749095 | ||||||
| chr3:15749101
|
G | T | 159 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(156): Show | 160 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.351+2649C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749101 | ||||||
| chr3:15749101
|
GT | G | 9 | a0001c0001t0008g0334a0001c0001t0008g0339a0001c0001t0015g0324others(6): Show | 9 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.351+2648delA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749101 | ||||||
| chr3:15749169
|
G | C | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.351+2581C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749169 | ||||||
| chr3:15749197
|
G | A | 1 | a0001c0001t0003g0261 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.351+2553C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749197 | ||||||
| chr3:15749268
|
G | A | 137 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.351+2482C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749268 | ||||||
| chr3:15749271
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.351+2479G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749271 | ||||||
| chr3:15749302
|
C | T | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.351+2448G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749302 | ||||||
| chr3:15749315
|
T | C | 3 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0150 | 3 | HG00621.hp2 NA18945.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.351+2435A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749315 | ||||||
| chr3:15749334
|
G | A | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.351+2416C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749334 | ||||||
| chr3:15749358
|
C | T | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+2392G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749358 | ||||||
| chr3:15749360
|
C | T | 4 | a0001c0001t0016g0327a0001c0001t0016g0328a0001c0001t0016g0330others(1): Show | 4 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+2390G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749360 | ||||||
| chr3:15749493
|
C | A | 3 | a0001c0007t0021g0302a0001c0007t0021g0303a0003c0013t0052g0293 | 3 | HG01884.hp2 NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+2257G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749493 | ||||||
| chr3:15749601
|
T | C | 2 | a0001c0001t0003g0253a0001c0001t0003g0271 | 2 | HG00733.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.351+2149A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749601 | ||||||
| chr3:15749772
|
G | A | 129 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.351+1978C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15749772 | ||||||
| chr3:15750046
|
G | A | 39 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(36): Show | 40 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.351+1704C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750046 | ||||||
| chr3:15750164
|
A | G | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.351+1586T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750164 | ||||||
| chr3:15750243
|
C | T | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.351+1507G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750243 | ||||||
| chr3:15750339
|
A | C | 1 | a0001c0001t0003g0270 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.351+1411T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750339 | ||||||
| chr3:15750447
|
C | T | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.351+1303G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750447 | ||||||
| chr3:15750808
|
G | A | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.351+942C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750808 | ||||||
| chr3:15750889
|
A | G | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+861T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750889 | ||||||
| chr3:15750967
|
T | G | 294 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(291): Show | 295 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.351+783A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15750967 | ||||||
| chr3:15751004
|
G | A | 1 | a0001c0002t0055g0321 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.351+746C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751004 | ||||||
| chr3:15751030
|
A | G | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.351+720T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751030 | ||||||
| chr3:15751114
|
T | C | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.351+636A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751114 | ||||||
| chr3:15751241
|
A | G | 131 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.351+509T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751241 | ||||||
| chr3:15751305
|
A | G | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.351+445T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751305 | ||||||
| chr3:15751504
|
T | G | 2 | a0001c0003t0018g0232a0001c0003t0018g0233 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.351+246A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751504 | ||||||
| chr3:15751558
|
C | T | 2 | a0001c0003t0005g0281a0001c0003t0005g0282 | 2 | HG01109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.351+192G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751558 | ||||||
| chr3:15751561
|
G | A | 25 | a0001c0001t0044g0178a0001c0002t0001g0119a0001c0002t0001g0120others(22): Show | 25 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.351+189C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751561 | ||||||
| chr3:15751565
|
C | T | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+185G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751565 | ||||||
| chr3:15751671
|
T | C | 1 | a0001c0001t0044g0178 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.351+79A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 4/27 | chr3 | 15751671 | ||||||
| chr3:15751988
|
A | G | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-168T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15751988 | ||||||
| chr3:15752049
|
A | G | 25 | a0001c0001t0044g0178a0001c0002t0001g0119a0001c0002t0001g0120others(22): Show | 25 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-229T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752049 | ||||||
| chr3:15752182
|
A | G | 1 | a0001c0002t0030g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.281-362T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752182 | ||||||
| chr3:15752291
|
C | T | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.281-471G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752291 | ||||||
| chr3:15752335
|
T | C | 21 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(18): Show | 21 | HG00408.hp2 HG01433.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.281-515A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752335 | ||||||
| chr3:15752356
|
T | C | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-536A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752356 | ||||||
| chr3:15752508
|
G | A | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.281-688C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752508 | ||||||
| chr3:15752558
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.281-738C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752558 | ||||||
| chr3:15752820
|
G | A | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.281-1000C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752820 | ||||||
| chr3:15752829
|
A | T | 1 | a0001c0002t0001g0157 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-1009T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752829 | ||||||
| chr3:15752880
|
G | T | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-1060C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15752880 | ||||||
| chr3:15753012
|
T | C | 1 | a0001c0001t0039g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.281-1192A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753012 | ||||||
| chr3:15753060
|
T | C | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.281-1240A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753060 | ||||||
| chr3:15753193
|
G | A | 15 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(12): Show | 15 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.281-1373C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753193 | ||||||
| chr3:15753266
|
A | G | 1 | a0001c0004t0009g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.281-1446T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753266 | ||||||
| chr3:15753495
|
A | G | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-1675T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753495 | ||||||
| chr3:15753504
|
C | T | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-1684G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753504 | ||||||
| chr3:15753507
|
A | G | 1 | a0001c0002t0001g0218 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.281-1687T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753507 | ||||||
| chr3:15753663
|
AG | A | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-1844delC | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753663 | ||||||
| chr3:15753671
|
G | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.281-1851C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753671 | ||||||
| chr3:15753723
|
G | GCCCA | 42 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-1904_281-1903i others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753723 | ||||||
| chr3:15753725
|
T | C | 42 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-1905A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753725 | ||||||
| chr3:15753727
|
G | C | 42 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-1907C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753727 | ||||||
| chr3:15753729
|
A | G | 42 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-1909T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753729 | ||||||
| chr3:15753760
|
T | C | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.281-1940A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753760 | ||||||
| chr3:15753869
|
G | A | 1 | a0001c0002t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.281-2049C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753869 | ||||||
| chr3:15753893
|
G | A | 1 | a0001c0001t0004g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.281-2073C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753893 | ||||||
| chr3:15753955
|
G | A | 1 | a0001c0004t0025g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281-2135C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15753955 | ||||||
| chr3:15754041
|
C | T | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-2221G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754041 | ||||||
| chr3:15754158
|
T | A | 1 | a0001c0002t0001g0191 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.281-2338A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754158 | ||||||
| chr3:15754170
|
T | C | 1 | a0004c0008t0002g0043 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.281-2350A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754170 | ||||||
| chr3:15754187
|
C | T | 1 | a0001c0002t0001g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.281-2367G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754187 | ||||||
| chr3:15754290
|
T | G | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-2470A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754290 | ||||||
| chr3:15754518
|
A | C | 1 | a0001c0001t0003g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.281-2698T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754518 | ||||||
| chr3:15754527
|
A | G | 1 | a0001c0002t0001g0157 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-2707T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754527 | ||||||
| chr3:15754706
|
C | T | 1 | a0001c0002t0001g0115 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.281-2886G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754706 | ||||||
| chr3:15754839
|
G | A | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.281-3019C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754839 | ||||||
| chr3:15754892
|
A | G | 294 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(291): Show | 295 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.281-3072T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754892 | ||||||
| chr3:15754986
|
C | T | 143 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(140): Show | 144 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.281-3166G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754986 | ||||||
| chr3:15754998
|
G | A | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.281-3178C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754998 | ||||||
| chr3:15754999
|
C | T | 42 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-3179G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15754999 | ||||||
| chr3:15755173
|
C | A | 23 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.281-3353G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755173 | ||||||
| chr3:15755208
|
G | A | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.281-3388C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755208 | ||||||
| chr3:15755339
|
A | G | 43 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(40): Show | 43 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.281-3519T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755339 | ||||||
| chr3:15755346
|
G | A | 127 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.281-3526C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755346 | ||||||
| chr3:15755453
|
G | A | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.281-3633C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755453 | ||||||
| chr3:15755690
|
G | A | 21 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.281-3870C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755690 | ||||||
| chr3:15755729
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.281-3909C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755729 | ||||||
| chr3:15755947
|
A | G | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.281-4127T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15755947 | ||||||
| chr3:15756133
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.281-4313C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756133 | ||||||
| chr3:15756279
|
T | C | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.281-4459A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756279 | ||||||
| chr3:15756382
|
T | C | 1 | a0001c0002t0030g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.281-4562A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756382 | ||||||
| chr3:15756399
|
A | G | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.281-4579T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756399 | ||||||
| chr3:15756430
|
C | T | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.281-4610G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756430 | ||||||
| chr3:15756533
|
A | T | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-4713T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756533 | ||||||
| chr3:15756535
|
G | T | 2 | a0001c0002t0001g0158a0001c0002t0045g0161 | 2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.281-4715C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756535 | ||||||
| chr3:15756589
|
C | T | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-4769G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756589 | ||||||
| chr3:15756725
|
G | C | 22 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.281-4905C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756725 | ||||||
| chr3:15756739
|
A | G | 280 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(277): Show | 281 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.281-4919T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756739 | ||||||
| chr3:15756834
|
G | A | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.281-5014C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15756834 | ||||||
| chr3:15757210
|
T | C | 2 | a0001c0001t0008g0334a0001c0001t0008g0339 | 2 | NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.281-5390A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757210 | ||||||
| chr3:15757486
|
G | A | 1 | a0001c0002t0001g0114 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.281-5666C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757486 | ||||||
| chr3:15757682
|
G | A | 24 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(21): Show | 24 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.281-5862C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757682 | ||||||
| chr3:15757723
|
C | A | 1 | a0001c0002t0001g0114 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.281-5903G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757723 | ||||||
| chr3:15757800
|
C | T | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.281-5980G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757800 | ||||||
| chr3:15757908
|
T | C | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.281-6088A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15757908 | ||||||
| chr3:15758078
|
G | T | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.281-6258C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758078 | ||||||
| chr3:15758391
|
G | A | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0036 | 3 | HG02622.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.281-6571C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758391 | ||||||
| chr3:15758468
|
T | G | 53 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(50): Show | 53 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.281-6648A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758468 | ||||||
| chr3:15758486
|
T | C | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.281-6666A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758486 | ||||||
| chr3:15758740
|
A | G | 1 | a0001c0001t0006g0315 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.281-6920T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758740 | ||||||
| chr3:15758866
|
C | T | 11 | a0001c0001t0008g0334a0001c0001t0008g0338a0001c0001t0008g0339others(8): Show | 11 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-7046G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15758866 | ||||||
| chr3:15759233
|
C | T | 136 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(133): Show | 136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.280+7001G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15759233 | ||||||
| chr3:15759301
|
T | C | 256 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(253): Show | 257 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.280+6933A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15759301 | ||||||
| chr3:15759326
|
C | CA | 23 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.280+6907dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15759326 | ||||||
| chr3:15759693
|
C | A | 24 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(21): Show | 24 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.280+6541G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15759693 | ||||||
| chr3:15760032
|
G | A | 1 | a0001c0002t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+6202C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760032 | ||||||
| chr3:15760056
|
ACTAT | A | 23 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.280+6174_280+6177d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760056 | ||||||
| chr3:15760161
|
G | A | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.280+6073C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760161 | ||||||
| chr3:15760336
|
A | G | 1 | a0001c0003t0005g0282 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.280+5898T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760336 | ||||||
| chr3:15760390
|
A | G | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280+5844T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760390 | ||||||
| chr3:15760624
|
A | T | 51 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(48): Show | 51 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.280+5610T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760624 | ||||||
| chr3:15760697
|
G | C | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.280+5537C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760697 | ||||||
| chr3:15760892
|
C | T | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.280+5342G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15760892 | ||||||
| chr3:15761064
|
G | T | 1 | a0001c0002t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+5170C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761064 | ||||||
| chr3:15761337
|
T | C | 40 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(37): Show | 41 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.280+4897A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761337 | ||||||
| chr3:15761740
|
T | G | 1 | a0001c0010t0012g0317 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.280+4494A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761740 | ||||||
| chr3:15761757
|
C | G | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.280+4477G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761757 | ||||||
| chr3:15761762
|
G | A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.280+4472C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761762 | ||||||
| chr3:15761797
|
T | A | 1 | a0001c0002t0001g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280+4437A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761797 | ||||||
| chr3:15761981
|
T | C | 338 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.280+4253A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761981 | ||||||
| chr3:15761998
|
C | T | 1 | a0001c0001t0002g0060 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.280+4236G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15761998 | ||||||
| chr3:15762154
|
C | T | 1 | a0001c0002t0001g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280+4080G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762154 | ||||||
| chr3:15762188
|
T | TA | 34 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0003g0256others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.280+4045dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762188 | ||||||
| chr3:15762189
|
A | T | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.280+4045T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762189 | ||||||
| chr3:15762189
|
AAAAAAAA others(23): Show |
A | 3 | a0001c0002t0001g0173a0001c0007t0021g0302a0001c0007t0021g0303 | 3 | NA19001.hp1 NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.280+4015_280+4044d others(32): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762189 | ||||||
| chr3:15762190
|
AAAAAAAA others(22): Show |
A | 126 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.280+4015_280+4043d others(31): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762190 | ||||||
| chr3:15762191
|
AAAAAAAA others(21): Show |
A | 9 | a0001c0002t0001g0206a0001c0002t0001g0213a0001c0002t0001g0223others(6): Show | 9 | HG01361.hp1 HG01361.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.280+4015_280+4042d others(30): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762191 | ||||||
| chr3:15762203
|
A | C | 4 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031others(1): Show | 4 | HG01934.hp1 HG02273.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+4031T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762203 | ||||||
| chr3:15762207
|
A | C | 1 | a0001c0001t0026g0006 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.280+4027T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762207 | ||||||
| chr3:15762209
|
A | AC | 11 | a0001c0001t0003g0266a0001c0001t0004g0238a0001c0001t0004g0239others(8): Show | 11 | HG01891.hp1 HG02056.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.280+4024_280+4025i others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762209 | ||||||
| chr3:15762209
|
A | C | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.280+4025T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762209 | ||||||
| chr3:15762212
|
A | AAAC | 52 | a0001c0001t0002g0012a0001c0001t0002g0019a0001c0001t0002g0026others(49): Show | 52 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.280+4021_280+4022i others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762212 | ||||||
| chr3:15762212
|
AAC | A | 6 | a0001c0004t0009g0294a0001c0004t0009g0296a0001c0004t0009g0299others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+4020_280+4021d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762212 | ||||||
| chr3:15762213
|
AC | A | 3 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306 | 3 | HG01884.hp1 HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.280+4020delG | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762213 | ||||||
| chr3:15762214
|
C | A | 83 | a0001c0001t0002g0012a0001c0001t0002g0019a0001c0001t0002g0026others(80): Show | 83 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.280+4020G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762214 | ||||||
| chr3:15762214
|
C | CAA | 43 | a0001c0001t0002g0011a0001c0001t0002g0013a0001c0001t0002g0014others(40): Show | 44 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.280+4018_280+4019d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762214 | ||||||
| chr3:15762217
|
A | C | 5 | a0001c0002t0001g0225a0001c0003t0018g0232a0001c0003t0018g0233others(2): Show | 5 | HG01081.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+4017T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762217 | ||||||
| chr3:15762219
|
C | A | 43 | a0001c0001t0002g0076a0001c0001t0002g0087a0001c0001t0006g0304others(40): Show | 43 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.280+4015G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762219 | ||||||
| chr3:15762221
|
A | AC | 48 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(45): Show | 48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.280+4012_280+4013i others(3): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762221 | ||||||
| chr3:15762221
|
A | ACAAC | 3 | a0001c0001t0002g0076a0001c0001t0002g0087a0001c0001t0034g0102 | 3 | NA19011.hp2 NA19087.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.280+4012_280+4013i others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762221 | ||||||
| chr3:15762222
|
A | C | 50 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(47): Show | 51 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.280+4012T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762222 | ||||||
| chr3:15762223
|
A | C | 6 | a0001c0001t0010g0274a0001c0001t0010g0275a0001c0001t0010g0276others(3): Show | 6 | HG01934.hp2 HG02055.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+4011T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762223 | ||||||
| chr3:15762224
|
A | C | 24 | a0001c0001t0003g0268a0001c0001t0003g0272a0001c0001t0004g0238others(21): Show | 24 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.280+4010T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762224 | ||||||
| chr3:15762492
|
T | C | 1 | a0001c0002t0038g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.280+3742A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762492 | ||||||
| chr3:15762834
|
T | C | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+3400A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762834 | ||||||
| chr3:15762835
|
C | T | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+3399G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15762835 | ||||||
| chr3:15763046
|
T | C | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280+3188A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763046 | ||||||
| chr3:15763051
|
T | G | 53 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(50): Show | 53 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.280+3183A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763051 | ||||||
| chr3:15763244
|
T | C | 3 | a0001c0002t0011g0236a0001c0002t0011g0237a0003c0015t0011g0234 | 3 | HG01255.hp1 HG01993.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.280+2990A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763244 | ||||||
| chr3:15763550
|
A | G | 4 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0160others(1): Show | 4 | NA18948.hp2 NA18954.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+2684T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763550 | ||||||
| chr3:15763658
|
A | G | 253 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(250): Show | 254 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.280+2576T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763658 | ||||||
| chr3:15763689
|
G | A | 1 | a0001c0002t0011g0235 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.280+2545C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763689 | ||||||
| chr3:15763717
|
A | G | 296 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(293): Show | 297 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.280+2517T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763717 | ||||||
| chr3:15763753
|
G | A | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+2481C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763753 | ||||||
| chr3:15763865
|
T | G | 1 | a0001c0002t0001g0123 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.280+2369A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763865 | ||||||
| chr3:15763874
|
T | C | 1 | a0001c0002t0001g0131 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.280+2360A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763874 | ||||||
| chr3:15763982
|
C | T | 1 | a0001c0001t0058g0329 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.280+2252G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15763982 | ||||||
| chr3:15764203
|
A | G | 1 | a0002c0006t0001g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.280+2031T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764203 | ||||||
| chr3:15764386
|
T | A | 1 | a0001c0001t0002g0048 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.280+1848A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764386 | ||||||
| chr3:15764541
|
GA | G | 152 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.280+1692delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764541 | ||||||
| chr3:15764569
|
A | T | 1 | a0001c0001t0002g0062 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.280+1665T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764569 | ||||||
| chr3:15764755
|
C | T | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+1479G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764755 | ||||||
| chr3:15764964
|
A | G | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.280+1270T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764964 | ||||||
| chr3:15764982
|
C | CTGTT | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.280+1251_280+1252i others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764982 | ||||||
| chr3:15764998
|
C | T | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.280+1236G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15764998 | ||||||
| chr3:15765013
|
A | C | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.280+1221T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765013 | ||||||
| chr3:15765181
|
T | A | 1 | a0001c0002t0001g0132 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.280+1053A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765181 | ||||||
| chr3:15765314
|
A | G | 2 | a0001c0002t0001g0170a0001c0002t0001g0171 | 2 | HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.280+920T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765314 | ||||||
| chr3:15765486
|
G | T | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.280+748C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765486 | ||||||
| chr3:15765612
|
C | T | 1 | a0001c0001t0016g0327 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.280+622G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765612 | ||||||
| chr3:15765690
|
A | G | 1 | a0001c0001t0006g0314 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.280+544T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765690 | ||||||
| chr3:15765702
|
T | C | 1 | a0001c0002t0001g0192 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.280+532A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765702 | ||||||
| chr3:15765722
|
C | A | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.280+512G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765722 | ||||||
| chr3:15765839
|
C | A | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.280+395G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765839 | ||||||
| chr3:15765847
|
CA | C | 60 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0056others(57): Show | 60 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.280+386delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765847 | ||||||
| chr3:15765847
|
CAA | C | 181 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(178): Show | 182 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.280+385_280+386del others(2): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765847 | ||||||
| chr3:15765881
|
G | A | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.280+353C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765881 | ||||||
| chr3:15765907
|
G | A | 6 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0036g0104others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+327C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765907 | ||||||
| chr3:15765919
|
C | A | 50 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(47): Show | 50 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.280+315G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15765919 | ||||||
| chr3:15766052
|
A | G | 1 | a0001c0002t0001g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.280+182T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15766052 | ||||||
| chr3:15766091
|
T | C | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.280+143A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15766091 | ||||||
| chr3:15766108
|
T | A | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.280+126A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15766108 | ||||||
| chr3:15766185
|
A | G | 4 | a0001c0002t0014g0109a0001c0002t0014g0110a0001c0002t0014g0111others(1): Show | 4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+49T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15766185 | ||||||
| chr3:15766218
|
T | A | 136 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(133): Show | 136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.280+16A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 3/27 | chr3 | 15766218 | ||||||
| chr3:15766326
|
G | A | 1 | a0001c0002t0049g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.202-14C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766326 | ||||||
| chr3:15766496
|
C | A | 1 | a0001c0002t0001g0199 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.202-184G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766496 | ||||||
| chr3:15766581
|
A | G | 99 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.202-269T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766581 | ||||||
| chr3:15766646
|
T | C | 12 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-334A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766646 | ||||||
| chr3:15766690
|
A | C | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.202-378T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766690 | ||||||
| chr3:15766851
|
TGATA | T | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.202-543_202-540del others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766851 | ||||||
| chr3:15766947
|
G | C | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-635C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15766947 | ||||||
| chr3:15767097
|
T | C | 2 | a0001c0002t0001g0134a0001c0002t0042g0133 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.202-785A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767097 | ||||||
| chr3:15767165
|
A | C | 136 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(133): Show | 136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.202-853T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767165 | ||||||
| chr3:15767200
|
C | T | 7 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0245others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-888G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767200 | ||||||
| chr3:15767329
|
TACTC | T | 23 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-1021_202-1018d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767329 | ||||||
| chr3:15767352
|
C | T | 1 | a0001c0001t0002g0097 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.202-1040G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767352 | ||||||
| chr3:15767383
|
A | T | 264 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(261): Show | 265 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.202-1071T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767383 | ||||||
| chr3:15767600
|
G | A | 1 | a0001c0002t0007g0182 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.202-1288C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767600 | ||||||
| chr3:15767657
|
G | A | 1 | a0001c0002t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.202-1345C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767657 | ||||||
| chr3:15767682
|
A | G | 280 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(277): Show | 281 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.202-1370T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767682 | ||||||
| chr3:15767700
|
T | TA | 10 | a0001c0001t0003g0254a0001c0001t0003g0271a0001c0001t0008g0332others(7): Show | 10 | HG00140.hp1 HG01167.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.202-1389dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
T | TAA | 6 | a0001c0001t0003g0261a0001c0001t0003g0263a0001c0001t0003g0266others(3): Show | 6 | HG01243.hp1 HG02056.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-1390_202-1389d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0003g0259 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.202-1399_202-1389d others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0003g0256 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.202-1400_202-1389d others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
T | TAAAAAAA others(12): Show |
1 | a0001c0001t0016g0328 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.202-1407_202-1389d others(21): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TA | T | 21 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0272others(18): Show | 21 | HG00099.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.202-1389delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAA | T | 9 | a0001c0002t0001g0196a0001c0002t0001g0200a0001c0002t0001g0201others(6): Show | 9 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-1390_202-1389d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAA | T | 7 | a0001c0002t0001g0117a0001c0002t0001g0118a0001c0002t0001g0134others(4): Show | 7 | HG01255.hp1 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-1391_202-1389d others(5): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAA | T | 16 | a0001c0002t0001g0116a0001c0002t0001g0193a0001c0002t0001g0194others(13): Show | 16 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.202-1392_202-1389d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAA | T | 7 | a0001c0002t0001g0197a0001c0002t0001g0199a0001c0002t0001g0204others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-1393_202-1389d others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAAAA others(3): Show |
T | 4 | a0001c0001t0004g0239a0001c0001t0004g0240a0001c0001t0004g0246others(1): Show | 4 | HG02486.hp1 HG02602.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-1398_202-1389d others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAAAA others(4): Show |
T | 5 | a0001c0001t0004g0238a0001c0001t0004g0245a0001c0001t0004g0247others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-1399_202-1389d others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAAAA others(5): Show |
T | 9 | a0001c0003t0005g0282a0001c0003t0005g0287a0001c0003t0005g0289others(6): Show | 9 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.202-1400_202-1389d others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAAAA others(6): Show |
T | 12 | a0001c0003t0005g0281a0001c0003t0005g0285a0001c0003t0005g0286others(9): Show | 12 | HG01168.hp2 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-1401_202-1389d others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAAAA others(10): Show |
T | 19 | a0001c0001t0002g0011a0001c0001t0002g0019a0001c0001t0002g0027others(16): Show | 20 | HG00597.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.202-1405_202-1389d others(19): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAAAA others(11): Show |
T | 80 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.202-1406_202-1389d others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAAAA others(12): Show |
T | 2 | a0001c0001t0002g0089a0001c0001t0002g0090 | 2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.202-1407_202-1389d others(21): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAAAA others(14): Show |
T | 1 | a0001c0001t0004g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202-1409_202-1389d others(23): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAAAA others(19): Show |
T | 7 | a0001c0002t0001g0115a0001c0002t0001g0183a0001c0002t0001g0191others(4): Show | 7 | HG02300.hp1 HG02300.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-1414_202-1389d others(28): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767700
|
TAAAAAAA others(20): Show |
T | 87 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(84): Show | 87 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.202-1415_202-1389d others(29): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767700 | ||||||
| chr3:15767751
|
G | A | 1 | a0001c0004t0009g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.202-1439C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767751 | ||||||
| chr3:15767783
|
G | C | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.202-1471C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767783 | ||||||
| chr3:15767786
|
G | C | 1 | a0001c0002t0001g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.202-1474C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767786 | ||||||
| chr3:15767813
|
G | A | 6 | a0001c0002t0001g0134a0001c0002t0014g0109a0001c0002t0014g0110others(3): Show | 6 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-1501C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767813 | ||||||
| chr3:15767908
|
CAACAAA | C | 11 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-1602_202-1597d others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767908 | ||||||
| chr3:15767910
|
AC | A | 15 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.202-1599delG | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767910 | ||||||
| chr3:15767914
|
A | C | 15 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.202-1602T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15767914 | ||||||
| chr3:15768098
|
A | G | 2 | a0001c0002t0001g0112a0001c0002t0001g0113 | 2 | NA19063.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.202-1786T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768098 | ||||||
| chr3:15768390
|
C | T | 24 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(21): Show | 24 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.202-2078G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768390 | ||||||
| chr3:15768613
|
T | C | 1 | a0001c0002t0001g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.202-2301A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768613 | ||||||
| chr3:15768640
|
A | C | 1 | a0001c0002t0030g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.202-2328T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768640 | ||||||
| chr3:15768687
|
T | C | 2 | a0001c0002t0001g0163a0001c0002t0001g0164 | 2 | NA18969.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.202-2375A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768687 | ||||||
| chr3:15768777
|
G | A | 2 | a0001c0002t0001g0193a0001c0002t0001g0196 | 2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.202-2465C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768777 | ||||||
| chr3:15768802
|
A | G | 136 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(133): Show | 136 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.202-2490T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15768802 | ||||||
| chr3:15769071
|
G | A | 1 | a0001c0001t0033g0101 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.202-2759C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769071 | ||||||
| chr3:15769091
|
A | G | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.202-2779T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769091 | ||||||
| chr3:15769098
|
C | T | 280 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(277): Show | 281 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.202-2786G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769098 | ||||||
| chr3:15769136
|
A | G | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-2824T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769136 | ||||||
| chr3:15769158
|
G | C | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.202-2846C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769158 | ||||||
| chr3:15769410
|
C | T | 2 | a0001c0001t0010g0276a0001c0001t0010g0278 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.202-3098G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769410 | ||||||
| chr3:15769426
|
A | T | 4 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0160others(1): Show | 4 | NA18948.hp2 NA18954.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-3114T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769426 | ||||||
| chr3:15769540
|
A | G | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-3228T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769540 | ||||||
| chr3:15769725
|
G | A | 4 | a0001c0002t0014g0109a0001c0002t0014g0110a0001c0002t0014g0111others(1): Show | 4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-3413C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769725 | ||||||
| chr3:15769840
|
A | G | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.202-3528T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15769840 | ||||||
| chr3:15770007
|
C | T | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.202-3695G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770007 | ||||||
| chr3:15770033
|
A | G | 1 | a0001c0002t0046g0153 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.202-3721T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770033 | ||||||
| chr3:15770034
|
A | T | 1 | a0001c0002t0046g0153 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.202-3722T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770034 | ||||||
| chr3:15770037
|
T | A | 1 | a0001c0002t0046g0153 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.202-3725A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770037 | ||||||
| chr3:15770037
|
T | TA | 7 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0099others(4): Show | 7 | HG00621.hp1 HG02129.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-3726dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770037 | ||||||
| chr3:15770119
|
T | A | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.202-3807A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770119 | ||||||
| chr3:15770342
|
GAA | G | 21 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.202-4032_202-4031d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770342 | ||||||
| chr3:15770396
|
T | C | 1 | a0001c0001t0004g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202-4084A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770396 | ||||||
| chr3:15770413
|
C | CAT | 86 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(83): Show | 87 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.202-4103_202-4102d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770413 | ||||||
| chr3:15770413
|
C | CATAT | 13 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(10): Show | 13 | HG01099.hp1 HG01891.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.202-4105_202-4102d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770413 | ||||||
| chr3:15770413
|
C | T | 1 | a0001c0002t0040g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.202-4101G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770413 | ||||||
| chr3:15770413
|
CAT | C | 38 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(35): Show | 38 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.202-4103_202-4102d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770413 | ||||||
| chr3:15770567
|
C | T | 43 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(40): Show | 44 | HG00408.hp2 HG00423.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.202-4255G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770567 | ||||||
| chr3:15770578
|
T | C | 42 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.202-4266A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770578 | ||||||
| chr3:15770751
|
G | A | 3 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0024g0004 | 3 | HG01069.hp2 NA18948.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.202-4439C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770751 | ||||||
| chr3:15770836
|
G | A | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-4524C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770836 | ||||||
| chr3:15770873
|
G | C | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.202-4561C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15770873 | ||||||
| chr3:15771015
|
G | C | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.202-4703C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771015 | ||||||
| chr3:15771324
|
C | G | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.202-5012G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771324 | ||||||
| chr3:15771409
|
C | CA | 103 | a0001c0001t0001g0166a0001c0001t0015g0326a0001c0001t0033g0101others(100): Show | 103 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.202-5098dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771409 | ||||||
| chr3:15771409
|
C | CAA | 24 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0194others(21): Show | 24 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.202-5099_202-5098d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771409 | ||||||
| chr3:15771409
|
CA | C | 40 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(37): Show | 40 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.202-5098delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771409 | ||||||
| chr3:15771462
|
A | G | 2 | a0001c0009t0005g0283a0001c0009t0005g0284 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.202-5150T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771462 | ||||||
| chr3:15771514
|
G | C | 1 | a0001c0002t0001g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.202-5202C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771514 | ||||||
| chr3:15771560
|
A | G | 1 | a0001c0002t0001g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.202-5248T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771560 | ||||||
| chr3:15771739
|
C | A | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-5427G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771739 | ||||||
| chr3:15771740
|
G | T | 23 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-5428C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771740 | ||||||
| chr3:15771869
|
T | C | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.202-5557A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771869 | ||||||
| chr3:15771916
|
A | G | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-5604T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15771916 | ||||||
| chr3:15772109
|
T | C | 47 | a0001c0001t0001g0166a0001c0002t0001g0112a0001c0002t0001g0113others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.202-5797A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772109 | ||||||
| chr3:15772453
|
C | T | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.202-6141G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772453 | ||||||
| chr3:15772549
|
T | G | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.202-6237A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772549 | ||||||
| chr3:15772732
|
G | A | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-6420C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772732 | ||||||
| chr3:15772747
|
C | T | 9 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-6435G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772747 | ||||||
| chr3:15772782
|
G | C | 1 | a0001c0005t0012g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202-6470C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772782 | ||||||
| chr3:15772789
|
C | T | 5 | a0001c0005t0012g0319a0001c0005t0036g0104a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-6477G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772789 | ||||||
| chr3:15772790
|
G | T | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.202-6478C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772790 | ||||||
| chr3:15772812
|
G | C | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.202-6500C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15772812 | ||||||
| chr3:15773135
|
TA | T | 13 | a0001c0001t0002g0060a0001c0003t0005g0281a0001c0003t0005g0282others(10): Show | 13 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.202-6824delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773135 | ||||||
| chr3:15773228
|
T | C | 31 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0118others(28): Show | 31 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.202-6916A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773228 | ||||||
| chr3:15773279
|
G | A | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.202-6967C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773279 | ||||||
| chr3:15773400
|
G | A | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-7088C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773400 | ||||||
| chr3:15773403
|
T | C | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.202-7091A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773403 | ||||||
| chr3:15773592
|
G | A | 2 | a0001c0002t0001g0163a0001c0002t0001g0164 | 2 | NA18969.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.202-7280C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773592 | ||||||
| chr3:15773947
|
G | T | 1 | a0001c0001t0033g0101 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.202-7635C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15773947 | ||||||
| chr3:15774042
|
C | T | 1 | a0001c0002t0051g0279 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.202-7730G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774042 | ||||||
| chr3:15774229
|
T | C | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-7917A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774229 | ||||||
| chr3:15774250
|
A | G | 4 | a0001c0002t0014g0109a0001c0002t0014g0110a0001c0002t0014g0111others(1): Show | 4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.202-7938T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774250 | ||||||
| chr3:15774281
|
C | A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.202-7969G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774281 | ||||||
| chr3:15774644
|
A | G | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-8332T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774644 | ||||||
| chr3:15774717
|
A | G | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-8405T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774717 | ||||||
| chr3:15774819
|
C | T | 137 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.202-8507G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774819 | ||||||
| chr3:15774849
|
G | T | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-8537C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774849 | ||||||
| chr3:15774985
|
T | TCCTGCCT others(30): Show |
101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.202-8710_202-8674d others(39): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15774985 | ||||||
| chr3:15775029
|
A | C | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-8717T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775029 | ||||||
| chr3:15775040
|
C | T | 1 | a0001c0002t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.202-8728G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775040 | ||||||
| chr3:15775297
|
G | A | 1 | a0001c0002t0040g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.202-8985C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775297 | ||||||
| chr3:15775378
|
C | T | 1 | a0001c0001t0002g0097 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.202-9066G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775378 | ||||||
| chr3:15775540
|
T | C | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-9228A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775540 | ||||||
| chr3:15775561
|
A | C | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.202-9249T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775561 | ||||||
| chr3:15775660
|
A | G | 1 | a0001c0002t0040g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.202-9348T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775660 | ||||||
| chr3:15775811
|
C | A | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-9499G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775811 | ||||||
| chr3:15775811
|
C | T | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.202-9499G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775811 | ||||||
| chr3:15775876
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.202-9564G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775876 | ||||||
| chr3:15775917
|
A | G | 1 | a0001c0005t0012g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202-9605T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775917 | ||||||
| chr3:15775995
|
T | G | 280 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(277): Show | 281 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.202-9683A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15775995 | ||||||
| chr3:15776095
|
T | A | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-9783A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15776095 | ||||||
| chr3:15776134
|
A | G | 1 | a0001c0001t0002g0059 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.202-9822T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15776134 | ||||||
| chr3:15776623
|
G | C | 1 | a0001c0002t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.202-10311C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15776623 | ||||||
| chr3:15776936
|
T | A | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-10624A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15776936 | ||||||
| chr3:15777071
|
C | T | 23 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.202-10759G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777071 | ||||||
| chr3:15777084
|
G | T | 1 | a0001c0002t0001g0214 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.202-10772C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777084 | ||||||
| chr3:15777107
|
C | T | 1 | a0001c0002t0042g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.202-10795G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777107 | ||||||
| chr3:15777140
|
A | G | 294 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(291): Show | 295 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.202-10828T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777140 | ||||||
| chr3:15777222
|
T | C | 280 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(277): Show | 281 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.202-10910A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777222 | ||||||
| chr3:15777271
|
CA | C | 21 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0010g0274others(18): Show | 21 | HG01109.hp2 HG01168.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.202-10960delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777271 | ||||||
| chr3:15777271
|
CAA | C | 213 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(210): Show | 214 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.202-10961_202-1096 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777271 | ||||||
| chr3:15777271
|
CAAA | C | 45 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(42): Show | 45 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.202-10962_202-1096 others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777271 | ||||||
| chr3:15777388
|
C | T | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-11076G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777388 | ||||||
| chr3:15777577
|
CAT | C | 3 | a0001c0003t0005g0288a0001c0003t0005g0290a0001c0003t0005g0291 | 3 | HG02280.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.202-11267_202-1126 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777577 | ||||||
| chr3:15777586
|
T | G | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-11274A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777586 | ||||||
| chr3:15777684
|
G | A | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-11372C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777684 | ||||||
| chr3:15777812
|
C | G | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.202-11500G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777812 | ||||||
| chr3:15777849
|
T | TAC | 31 | a0001c0001t0003g0258a0001c0001t0003g0268a0001c0001t0039g0107others(28): Show | 31 | HG00642.hp1 HG01515.hp1 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.202-11539_202-1153 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
T | TACAC | 41 | a0001c0001t0003g0259a0001c0001t0003g0269a0001c0001t0004g0238others(38): Show | 41 | HG00099.hp1 HG00423.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.202-11541_202-1153 others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
T | TACACAC | 36 | a0001c0001t0003g0253a0001c0001t0003g0270a0001c0001t0003g0271others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.202-11543_202-1153 others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
T | TACACACA others(1): Show |
26 | a0001c0001t0001g0166a0001c0001t0003g0272a0001c0001t0004g0239others(23): Show | 26 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.202-11545_202-1153 others(12): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
T | TACACACA others(3): Show |
15 | a0001c0001t0003g0273a0001c0001t0008g0331a0001c0001t0008g0335others(12): Show | 15 | HG00639.hp1 HG00738.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.202-11547_202-1153 others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
T | TACACACA others(5): Show |
7 | a0001c0001t0008g0336a0001c0002t0001g0114a0001c0002t0001g0130others(4): Show | 7 | HG01255.hp1 HG02257.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-11549_202-1153 others(16): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
T | TACACACA others(7): Show |
5 | a0001c0001t0016g0330a0001c0001t0058g0329a0001c0002t0001g0148others(2): Show | 5 | HG01109.hp1 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-11551_202-1153 others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
T | TACACACA others(9): Show |
1 | a0003c0015t0011g0234 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.202-11553_202-1153 others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
T | TACACACA others(11): Show |
1 | a0001c0001t0008g0337 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.202-11555_202-1153 others(22): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
T | TACACACA others(15): Show |
2 | a0001c0002t0001g0123a0001c0002t0001g0149 | 2 | HG00558.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.202-11559_202-1153 others(26): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
TAC | T | 14 | a0001c0001t0003g0256a0001c0001t0003g0260a0001c0001t0003g0264others(11): Show | 14 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.202-11539_202-1153 others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
TACAC | T | 7 | a0001c0001t0002g0011a0001c0001t0002g0036a0001c0001t0002g0037others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-11541_202-1153 others(8): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
TACACAC | T | 14 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0003g0254others(11): Show | 14 | HG01123.hp2 HG01167.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.202-11543_202-1153 others(10): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
TACACACA others(3): Show |
T | 6 | a0001c0001t0002g0033a0001c0001t0002g0051a0001c0004t0009g0297others(3): Show | 6 | HG02622.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-11547_202-1153 others(14): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
TACACACA others(5): Show |
T | 53 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0018others(50): Show | 54 | HG00408.hp2 HG00423.hp2 HG01433.hp2 others(51): Show |
intron_variant | MODIFIER | c.202-11549_202-1153 others(16): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
TACACACA others(7): Show |
T | 12 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(9): Show | 12 | HG02258.hp1 HG02647.hp2 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-11551_202-1153 others(18): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777849
|
TACACACA others(9): Show |
T | 39 | a0001c0001t0002g0052a0001c0001t0002g0055a0001c0001t0002g0056others(36): Show | 39 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.202-11553_202-1153 others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777849 | ||||||
| chr3:15777886
|
A | C | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-11574T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777886 | ||||||
| chr3:15777888
|
ACACACAC others(8): Show |
A | 1 | a0001c0001t0002g0100 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.202-11591_202-1157 others(19): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777888 | ||||||
| chr3:15777892
|
ACACACAC others(4): Show |
A | 1 | a0001c0001t0002g0039 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.202-11591_202-1158 others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777892 | ||||||
| chr3:15777902
|
A | C | 1 | a0001c0014t0037g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.202-11590T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777902 | ||||||
| chr3:15777903
|
C | CACACA | 5 | a0001c0002t0001g0131a0001c0002t0001g0159a0001c0002t0001g0190others(2): Show | 5 | HG01255.hp2 HG02004.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-11592_202-1159 others(9): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777903 | ||||||
| chr3:15777903
|
C | CACACACA others(2): Show |
4 | a0001c0001t0010g0274a0001c0001t0010g0275a0001c0002t0001g0160others(1): Show | 4 | HG01361.hp2 HG01934.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-11592_202-1159 others(13): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777903 | ||||||
| chr3:15777903
|
C | CACACACA others(4): Show |
2 | a0001c0002t0001g0142a0001c0002t0051g0279 | 2 | HG01099.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.202-11592_202-1159 others(15): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777903 | ||||||
| chr3:15777903
|
C | CACACACA others(10): Show |
1 | a0001c0002t0045g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.202-11592_202-1159 others(21): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777903 | ||||||
| chr3:15777998
|
T | C | 1 | a0001c0002t0001g0208 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.202-11686A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15777998 | ||||||
| chr3:15778006
|
C | G | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-11694G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778006 | ||||||
| chr3:15778455
|
A | C | 5 | a0001c0005t0020g0300a0001c0005t0020g0301a0001c0007t0021g0302others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-12143T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778455 | ||||||
| chr3:15778469
|
T | C | 4 | a0001c0002t0001g0162a0001c0002t0001g0163a0001c0002t0001g0164others(1): Show | 4 | HG00673.hp1 NA18962.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-12157A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778469 | ||||||
| chr3:15778545
|
G | C | 9 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0138others(6): Show | 9 | HG00642.hp1 HG01071.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-12233C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778545 | ||||||
| chr3:15778730
|
C | T | 12 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-12418G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778730 | ||||||
| chr3:15778865
|
G | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.202-12553C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15778865 | ||||||
| chr3:15779162
|
A | G | 1 | a0001c0002t0017g0228 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.202-12850T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779162 | ||||||
| chr3:15779284
|
G | T | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.202-12972C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779284 | ||||||
| chr3:15779429
|
T | C | 3 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042 | 3 | NA18950.hp2 NA18998.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.202-13117A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779429 | ||||||
| chr3:15779565
|
T | C | 2 | a0001c0002t0030g0010a0001c0014t0037g0105 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.202-13253A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779565 | ||||||
| chr3:15779614
|
T | C | 151 | a0001c0001t0001g0166a0001c0001t0006g0304a0001c0001t0006g0305others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.202-13302A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779614 | ||||||
| chr3:15779635
|
C | T | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-13323G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779635 | ||||||
| chr3:15779759
|
T | C | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.202-13447A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779759 | ||||||
| chr3:15779763
|
T | C | 1 | a0003c0015t0011g0234 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.202-13451A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779763 | ||||||
| chr3:15779779
|
C | T | 3 | a0001c0004t0009g0298a0001c0004t0009g0299a0001c0004t0025g0005 | 3 | HG02723.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.202-13467G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779779 | ||||||
| chr3:15779836
|
A | T | 1 | a0001c0001t0008g0338 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.202-13524T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779836 | ||||||
| chr3:15779980
|
C | T | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202-13668G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15779980 | ||||||
| chr3:15780001
|
T | C | 1 | a0001c0002t0017g0227 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.202-13689A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780001 | ||||||
| chr3:15780007
|
G | C | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202-13695C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780007 | ||||||
| chr3:15780080
|
T | C | 100 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(97): Show | 101 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.202-13768A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780080 | ||||||
| chr3:15780191
|
C | T | 280 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(277): Show | 281 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.202-13879G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780191 | ||||||
| chr3:15780276
|
C | A | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.202-13964G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780276 | ||||||
| chr3:15780401
|
T | C | 1 | a0001c0001t0004g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202-14089A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780401 | ||||||
| chr3:15780410
|
C | T | 1 | a0001c0001t0003g0262 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.202-14098G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780410 | ||||||
| chr3:15780488
|
T | C | 1 | a0001c0002t0001g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.202-14176A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780488 | ||||||
| chr3:15780717
|
A | G | 1 | a0001c0001t0008g0332 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.202-14405T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780717 | ||||||
| chr3:15780804
|
A | G | 5 | a0001c0002t0001g0225a0001c0003t0018g0232a0001c0003t0018g0233others(2): Show | 5 | HG01081.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+14419T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780804 | ||||||
| chr3:15780932
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.201+14291T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15780932 | ||||||
| chr3:15781659
|
G | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | HG02155.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.201+13564C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15781659 | ||||||
| chr3:15781667
|
A | C | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+13556T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15781667 | ||||||
| chr3:15781787
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.201+13436A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15781787 | ||||||
| chr3:15781949
|
A | G | 102 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(99): Show | 103 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.201+13274T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15781949 | ||||||
| chr3:15781951
|
T | A | 1 | a0001c0001t0008g0338 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.201+13272A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15781951 | ||||||
| chr3:15782035
|
A | G | 294 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(291): Show | 295 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.201+13188T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782035 | ||||||
| chr3:15782043
|
T | C | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+13180A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782043 | ||||||
| chr3:15782073
|
T | C | 1 | a0001c0002t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.201+13150A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782073 | ||||||
| chr3:15782114
|
A | G | 1 | a0001c0001t0004g0251 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.201+13109T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782114 | ||||||
| chr3:15782189
|
C | T | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.201+13034G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782189 | ||||||
| chr3:15782424
|
A | T | 16 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(13): Show | 16 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.201+12799T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782424 | ||||||
| chr3:15782436
|
G | C | 1 | a0001c0001t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.201+12787C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782436 | ||||||
| chr3:15782525
|
C | G | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.201+12698G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782525 | ||||||
| chr3:15782619
|
T | C | 10 | a0001c0002t0001g0115a0001c0002t0001g0132a0001c0002t0001g0167others(7): Show | 10 | HG02015.hp2 HG02129.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+12604A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782619 | ||||||
| chr3:15782623
|
G | A | 1 | a0001c0001t0004g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.201+12600C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782623 | ||||||
| chr3:15782649
|
T | C | 1 | a0001c0001t0006g0315 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.201+12574A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782649 | ||||||
| chr3:15782803
|
C | A | 4 | a0001c0002t0014g0109a0001c0002t0014g0110a0001c0002t0014g0111others(1): Show | 4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+12420G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782803 | ||||||
| chr3:15782836
|
T | C | 1 | a0001c0001t0008g0339 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.201+12387A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15782836 | ||||||
| chr3:15783040
|
T | A | 1 | a0001c0002t0001g0224 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.201+12183A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783040 | ||||||
| chr3:15783118
|
A | C | 6 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0002t0001g0146others(3): Show | 6 | HG00558.hp2 HG02056.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+12105T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783118 | ||||||
| chr3:15783188
|
A | C | 1 | a0001c0002t0001g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.201+12035T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783188 | ||||||
| chr3:15783325
|
G | A | 1 | a0001c0002t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.201+11898C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783325 | ||||||
| chr3:15783329
|
T | C | 102 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(99): Show | 103 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.201+11894A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783329 | ||||||
| chr3:15783353
|
T | G | 157 | a0001c0001t0001g0166a0001c0001t0006g0304a0001c0001t0006g0305others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.201+11870A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783353 | ||||||
| chr3:15783383
|
T | C | 1 | a0001c0001t0004g0249 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.201+11840A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783383 | ||||||
| chr3:15783681
|
G | A | 24 | a0001c0001t0044g0178a0001c0002t0001g0119a0001c0002t0001g0120others(21): Show | 24 | HG00558.hp1 HG00639.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.201+11542C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15783681 | ||||||
| chr3:15784501
|
TA | T | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.201+10721delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784501 | ||||||
| chr3:15784601
|
G | GACCAATA others(9): Show |
263 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(260): Show | 264 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.201+10621_201+1062 others(20): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784601 | ||||||
| chr3:15784832
|
A | G | 293 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(290): Show | 294 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.201+10391T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784832 | ||||||
| chr3:15784849
|
C | G | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+10374G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784849 | ||||||
| chr3:15784903
|
A | G | 1 | a0001c0002t0001g0194 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.201+10320T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784903 | ||||||
| chr3:15784925
|
A | G | 275 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(272): Show | 276 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.201+10298T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784925 | ||||||
| chr3:15784936
|
C | G | 14 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(11): Show | 14 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.201+10287G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15784936 | ||||||
| chr3:15785107
|
T | C | 12 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+10116A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785107 | ||||||
| chr3:15785216
|
G | A | 2 | a0001c0001t0002g0055a0001c0001t0029g0009 | 2 | NA18954.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.201+10007C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785216 | ||||||
| chr3:15785337
|
C | A | 5 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046others(2): Show | 5 | HG00423.hp2 NA18986.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+9886G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785337 | ||||||
| chr3:15785535
|
T | C | 2 | a0001c0002t0001g0134a0001c0002t0042g0133 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.201+9688A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785535 | ||||||
| chr3:15785699
|
A | AT | 9 | a0001c0002t0001g0136a0001c0002t0001g0137a0001c0002t0001g0138others(6): Show | 9 | HG00642.hp1 HG01071.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+9523dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785699 | ||||||
| chr3:15785937
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.201+9286A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15785937 | ||||||
| chr3:15786028
|
G | A | 5 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0212others(2): Show | 5 | HG01243.hp2 HG02300.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+9195C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786028 | ||||||
| chr3:15786047
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.201+9176C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786047 | ||||||
| chr3:15786105
|
A | T | 1 | a0001c0001t0002g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.201+9118T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786105 | ||||||
| chr3:15786157
|
C | A | 238 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(235): Show | 239 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.201+9066G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786157 | ||||||
| chr3:15786200
|
A | C | 2 | a0001c0002t0001g0134a0001c0002t0042g0133 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.201+9023T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786200 | ||||||
| chr3:15786361
|
T | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.201+8862A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786361 | ||||||
| chr3:15786395
|
T | C | 1 | a0001c0002t0017g0228 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.201+8828A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786395 | ||||||
| chr3:15786757
|
C | T | 254 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(251): Show | 255 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.201+8466G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15786757 | ||||||
| chr3:15787090
|
C | T | 2 | a0001c0001t0004g0238a0001c0001t0004g0239 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.201+8133G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787090 | ||||||
| chr3:15787094
|
G | A | 1 | a0001c0005t0012g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.201+8129C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787094 | ||||||
| chr3:15787304
|
G | T | 264 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(261): Show | 265 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.201+7919C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787304 | ||||||
| chr3:15787425
|
A | C | 254 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(251): Show | 255 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.201+7798T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787425 | ||||||
| chr3:15787435
|
G | A | 26 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.201+7788C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787435 | ||||||
| chr3:15787620
|
A | G | 135 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.201+7603T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787620 | ||||||
| chr3:15787820
|
A | G | 1 | a0001c0001t0003g0261 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.201+7403T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787820 | ||||||
| chr3:15787824
|
T | C | 3 | a0001c0001t0010g0276a0001c0001t0010g0277a0001c0001t0010g0278 | 3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.201+7399A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787824 | ||||||
| chr3:15787859
|
C | T | 5 | a0001c0005t0012g0318a0001c0005t0012g0319a0001c0005t0057g0323others(2): Show | 5 | HG02622.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+7364G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787859 | ||||||
| chr3:15787894
|
T | C | 1 | a0001c0002t0001g0192 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.201+7329A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15787894 | ||||||
| chr3:15788198
|
A | G | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.201+7025T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788198 | ||||||
| chr3:15788218
|
T | C | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.201+7005A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788218 | ||||||
| chr3:15788407
|
C | T | 1 | a0001c0002t0017g0227 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.201+6816G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788407 | ||||||
| chr3:15788510
|
G | A | 3 | a0001c0001t0010g0276a0001c0001t0010g0277a0001c0001t0010g0278 | 3 | HG02970.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.201+6713C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788510 | ||||||
| chr3:15788730
|
T | C | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.201+6493A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788730 | ||||||
| chr3:15788765
|
C | T | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.201+6458G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788765 | ||||||
| chr3:15788766
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.201+6457C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788766 | ||||||
| chr3:15788811
|
G | T | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.201+6412C>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788811 | ||||||
| chr3:15788902
|
C | T | 1 | a0001c0001t0008g0331 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.201+6321G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788902 | ||||||
| chr3:15788905
|
C | T | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.201+6318G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788905 | ||||||
| chr3:15788908
|
A | C | 18 | a0001c0001t0003g0260a0001c0001t0006g0304a0001c0001t0006g0305others(15): Show | 18 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.201+6315T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15788908 | ||||||
| chr3:15789085
|
C | G | 1 | a0001c0002t0001g0132 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.201+6138G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789085 | ||||||
| chr3:15789090
|
C | CT | 12 | a0001c0003t0005g0281a0001c0003t0005g0282a0001c0003t0005g0285others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.201+6132dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789090 | ||||||
| chr3:15789164
|
C | T | 8 | a0001c0001t0006g0306a0001c0001t0006g0307a0001c0001t0006g0308others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.201+6059G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789164 | ||||||
| chr3:15789369
|
C | T | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.201+5854G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789369 | ||||||
| chr3:15789413
|
C | T | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.201+5810G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789413 | ||||||
| chr3:15789437
|
T | A | 2 | a0001c0002t0001g0225a0001c0002t0030g0010 | 2 | HG01081.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.201+5786A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789437 | ||||||
| chr3:15789437
|
TAAAAA | T | 12 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+5781_201+5785d others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789437 | ||||||
| chr3:15789443
|
AAAAAG | A | 11 | a0001c0004t0009g0294a0001c0004t0009g0295a0001c0004t0009g0296others(8): Show | 11 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.201+5775_201+5779d others(7): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789443 | ||||||
| chr3:15789519
|
T | A | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.201+5704A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789519 | ||||||
| chr3:15789564
|
C | A | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.201+5659G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789564 | ||||||
| chr3:15789641
|
A | G | 1 | a0001c0002t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.201+5582T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789641 | ||||||
| chr3:15789780
|
T | A | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+5443A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15789780 | ||||||
| chr3:15790018
|
T | C | 153 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.201+5205A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790018 | ||||||
| chr3:15790138
|
G | A | 101 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(98): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.201+5085C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790138 | ||||||
| chr3:15790152
|
TAA | T | 5 | a0001c0001t0003g0256a0001c0001t0003g0257a0001c0001t0003g0258others(2): Show | 5 | NA18957.hp2 NA18961.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+5069_201+5070d others(4): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790152 | ||||||
| chr3:15790200
|
C | T | 7 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0127others(4): Show | 7 | NA18940.hp2 NA18942.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+5023G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790200 | ||||||
| chr3:15790263
|
T | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.201+4960A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790263 | ||||||
| chr3:15790422
|
T | A | 1 | a0001c0007t0031g0049 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.201+4801A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790422 | ||||||
| chr3:15790518
|
T | C | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.201+4705A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790518 | ||||||
| chr3:15790542
|
T | C | 1 | a0001c0001t0002g0050 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.201+4681A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790542 | ||||||
| chr3:15790784
|
T | G | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.201+4439A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790784 | ||||||
| chr3:15790828
|
T | C | 99 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(96): Show | 100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.201+4395A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790828 | ||||||
| chr3:15790848
|
T | C | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.201+4375A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790848 | ||||||
| chr3:15790876
|
A | G | 1 | a0001c0002t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.201+4347T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790876 | ||||||
| chr3:15790910
|
C | T | 130 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(127): Show | 130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.201+4313G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15790910 | ||||||
| chr3:15791040
|
C | T | 97 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(94): Show | 97 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.201+4183G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791040 | ||||||
| chr3:15791054
|
C | T | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+4169G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791054 | ||||||
| chr3:15791216
|
C | T | 3 | a0001c0002t0001g0119a0001c0002t0001g0120a0001c0002t0001g0121 | 3 | HG01978.hp1 HG02148.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.201+4007G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791216 | ||||||
| chr3:15791352
|
TAACTTCA others(28): Show |
T | 16 | a0001c0001t0008g0331a0001c0001t0008g0332a0001c0001t0008g0334others(13): Show | 16 | HG00140.hp1 HG01261.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.201+3836_201+3870d others(37): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791352 | ||||||
| chr3:15791823
|
C | T | 1 | a0001c0002t0001g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.201+3400G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791823 | ||||||
| chr3:15791833
|
C | T | 2 | a0001c0010t0012g0316a0001c0010t0012g0317 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.201+3390G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791833 | ||||||
| chr3:15791945
|
T | C | 3 | a0001c0004t0009g0298a0001c0004t0009g0299a0001c0004t0025g0005 | 3 | HG02723.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.201+3278A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15791945 | ||||||
| chr3:15792033
|
T | C | 13 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(10): Show | 13 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.201+3190A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792033 | ||||||
| chr3:15792059
|
T | A | 1 | a0001c0001t0002g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.201+3164A>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792059 | ||||||
| chr3:15792060
|
C | A | 1 | a0001c0001t0002g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.201+3163G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792060 | ||||||
| chr3:15792107
|
GA | G | 10 | a0001c0003t0005g0285a0001c0003t0005g0286a0001c0005t0012g0318others(7): Show | 10 | HG01168.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+3115delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792107 | ||||||
| chr3:15792146
|
C | T | 254 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(251): Show | 255 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.201+3077G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792146 | ||||||
| chr3:15792166
|
C | T | 1 | a0003c0015t0011g0234 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.201+3057G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792166 | ||||||
| chr3:15792396
|
C | G | 265 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(262): Show | 266 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.201+2827G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792396 | ||||||
| chr3:15792554
|
C | T | 1 | a0001c0001t0003g0254 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.201+2669G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792554 | ||||||
| chr3:15792813
|
T | G | 2 | a0001c0007t0021g0302a0001c0007t0021g0303 | 2 | NA19087.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.201+2410A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792813 | ||||||
| chr3:15792852
|
A | T | 1 | a0001c0002t0001g0123 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.201+2371T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15792852 | ||||||
| chr3:15793089
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.201+2134G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793089 | ||||||
| chr3:15793163
|
A | C | 1 | a0001c0002t0043g0122 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.201+2060T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793163 | ||||||
| chr3:15793189
|
A | G | 1 | a0001c0001t0002g0055 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.201+2034T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793189 | ||||||
| chr3:15793239
|
G | A | 280 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(277): Show | 281 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.201+1984C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793239 | ||||||
| chr3:15793322
|
A | C | 3 | a0001c0002t0001g0119a0001c0002t0001g0120a0001c0002t0001g0121 | 3 | HG01978.hp1 HG02148.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.201+1901T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793322 | ||||||
| chr3:15793568
|
A | G | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | HG02615.hp2 HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.201+1655T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793568 | ||||||
| chr3:15793653
|
A | C | 1 | a0001c0001t0003g0253 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.201+1570T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793653 | ||||||
| chr3:15793688
|
C | T | 1 | a0001c0001t0006g0305 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.201+1535G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793688 | ||||||
| chr3:15793720
|
C | T | 1 | a0001c0001t0006g0304 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.201+1503G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793720 | ||||||
| chr3:15793813
|
C | T | 1 | a0001c0002t0001g0115 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.201+1410G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793813 | ||||||
| chr3:15793882
|
A | T | 1 | a0001c0002t0001g0114 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.201+1341T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15793882 | ||||||
| chr3:15794070
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.201+1153A>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794070 | ||||||
| chr3:15794076
|
A | AATAC | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.201+1143_201+1146d others(6): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794076 | ||||||
| chr3:15794155
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.201+1068A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794155 | ||||||
| chr3:15794211
|
A | G | 4 | a0001c0003t0018g0232a0001c0003t0018g0233a0001c0003t0019g0230others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+1012T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794211 | ||||||
| chr3:15794309
|
G | A | 3 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100 | 3 | HG02129.hp1 NA18964.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.201+914C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794309 | ||||||
| chr3:15794328
|
T | TA | 107 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(104): Show | 108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.201+894dupT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794328 | ||||||
| chr3:15794328
|
T | TAA | 130 | a0001c0001t0001g0166a0001c0001t0002g0053a0001c0001t0002g0054others(127): Show | 130 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.201+893_201+894dup others(2): Show |
ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794328 | ||||||
| chr3:15794392
|
A | G | 1 | a0001c0002t0001g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.201+831T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794392 | ||||||
| chr3:15794411
|
C | G | 1 | a0001c0005t0036g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.201+812G>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794411 | ||||||
| chr3:15794461
|
C | T | 2 | a0001c0003t0005g0281a0001c0003t0005g0282 | 2 | HG01109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.201+762G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794461 | ||||||
| chr3:15794489
|
C | T | 1 | a0007c0016t0050g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.201+734G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794489 | ||||||
| chr3:15794589
|
TA | T | 237 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(234): Show | 238 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.201+633delT | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794589 | ||||||
| chr3:15794597
|
A | T | 2 | a0001c0005t0020g0300a0001c0005t0020g0301 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.201+626T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794597 | ||||||
| chr3:15794627
|
A | G | 2 | a0001c0002t0001g0112a0001c0002t0001g0113 | 2 | NA19063.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.201+596T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794627 | ||||||
| chr3:15794822
|
A | T | 1 | a0003c0013t0052g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.201+401T>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794822 | ||||||
| chr3:15794891
|
T | C | 1 | a0001c0005t0057g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.201+332A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794891 | ||||||
| chr3:15794995
|
G | A | 10 | a0001c0002t0001g0215a0001c0002t0001g0216a0001c0002t0001g0217others(7): Show | 10 | HG00140.hp2 HG00741.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.201+228C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15794995 | ||||||
| chr3:15795184
|
C | A | 1 | a0001c0005t0012g0319 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.201+39G>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15795184 | ||||||
| chr3:15795198
|
G | A | 1 | a0001c0003t0005g0292 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.201+25C>T | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15795198 | ||||||
| chr3:15795216
|
G | GT | 13 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(10): Show | 13 | HG01168.hp1 HG01169.hp2 HG01891.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.201+6dupA | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 2/27 | chr3 | 15795216 | ||||||
| chr3:15795461
|
G | C | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.118-155C>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795461 | ||||||
| chr3:15795473
|
T | C | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.118-167A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795473 | ||||||
| chr3:15795514
|
C | T | 4 | a0001c0002t0014g0109a0001c0002t0014g0110a0001c0002t0014g0111others(1): Show | 4 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-208G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795514 | ||||||
| chr3:15795558
|
T | C | 1 | a0001c0001t0004g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.118-252A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795558 | ||||||
| chr3:15795861
|
A | C | 21 | a0001c0001t0006g0304a0001c0001t0006g0305a0001c0001t0006g0306others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.117+544T>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795861 | ||||||
| chr3:15795913
|
T | C | 17 | a0001c0002t0001g0225a0001c0003t0005g0281a0001c0003t0005g0282others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.117+492A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15795913 | ||||||
| chr3:15796031
|
T | C | 51 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(48): Show | 51 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.117+374A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15796031 | ||||||
| chr3:15796070
|
T | C | 2 | a0001c0002t0017g0227a0001c0002t0017g0228 | 2 | HG00597.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.117+335A>G | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15796070 | ||||||
| chr3:15796149
|
A | G | 128 | a0001c0001t0001g0166a0001c0001t0044g0178a0001c0002t0001g0112others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.117+256T>C | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15796149 | ||||||
| chr3:15796277
|
C | T | 280 | a0001c0001t0001g0166a0001c0001t0002g0011a0001c0001t0002g0012others(277): Show | 281 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.117+128G>A | ANKRD28 | ENSG00000206560.12 | transcript | ENST00000683139.1 | protein_coding | 1/27 | chr3 | 15796277 |